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Marine Sponges as Pharmacy

Identifieur interne : 000293 ( Pmc/Corpus ); précédent : 000292; suivant : 000294

Marine Sponges as Pharmacy

Auteurs : Detmer Sipkema ; Maurice C. R. Franssen ; Ronald Osinga ; Johannes Tramper ; René H. Wijffels

Source :

RBID : PMC:7087563

Abstract

Marine sponges have been considered as a gold mine during the past 50 years, with respect to the diversity of their secondary metabolites. The biological effects of new metabolites from sponges have been reported in hundreds of scientific papers, and they are reviewed here. Sponges have the potential to provide future drugs against important diseases, such as cancer, a range of viral diseases, malaria, and inflammations. Although the molecular mode of action of most metabolites is still unclear, for a substantial number of compounds the mechanisms by which they interfere with the pathogenesis of a wide range of diseases have been reported. This knowledge is one of the key factors necessary to transform bioactive compounds into medicines. Sponges produce a plethora of chemical compounds with widely varying carbon skeletons, which have been found to interfere with pathogenesis at many different points. The fact that a particular disease can be fought at different points increases the chance of developing selective drugs for specific targets.


Url:
DOI: 10.1007/s10126-004-0405-5
PubMed: 15776313
PubMed Central: 7087563

Links to Exploration step

PMC:7087563

Le document en format XML

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</div1>
</back>
</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Mar Biotechnol (NY)</journal-id>
<journal-id journal-id-type="iso-abbrev">Mar. Biotechnol</journal-id>
<journal-title-group>
<journal-title>Marine Biotechnology (New York, N.y.)</journal-title>
</journal-title-group>
<issn pub-type="ppub">1436-2228</issn>
<issn pub-type="epub">1436-2236</issn>
<publisher>
<publisher-name>Springer-Verlag</publisher-name>
<publisher-loc>New York</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">15776313</article-id>
<article-id pub-id-type="pmc">7087563</article-id>
<article-id pub-id-type="publisher-id">405</article-id>
<article-id pub-id-type="doi">10.1007/s10126-004-0405-5</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Marine Sponges as Pharmacy</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Sipkema</surname>
<given-names>Detmer</given-names>
</name>
<address>
<phone>+31(0)317-482237</phone>
<fax>+31(0)317-485097</fax>
<email>detmer.sipkema@wur.nl</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Franssen</surname>
<given-names>Maurice C. R.</given-names>
</name>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Osinga</surname>
<given-names>Ronald</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tramper</surname>
<given-names>Johannes</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wijffels</surname>
<given-names>René H.</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<aff id="Aff1">
<label>1</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.4818.5</institution-id>
<institution-id institution-id-type="ISNI">0000000107915666</institution-id>
<institution>Wageningen University, Food and Bioprocess Engineering Group,</institution>
</institution-wrap>
8129, 6700 EV Wageningen, The Netherlands</aff>
<aff id="Aff2">
<label>2</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.4818.5</institution-id>
<institution-id institution-id-type="ISNI">0000000107915666</institution-id>
<institution>Wageningen University, Laboratory of Organic Chemistry,</institution>
</institution-wrap>
Dreijenplein 8, 6703 HB Wageningen, The Netherlands</aff>
</contrib-group>
<pub-date pub-type="epub">
<day>24</day>
<month>3</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="ppub">
<year>2005</year>
</pub-date>
<volume>7</volume>
<issue>3</issue>
<elocation-id>142</elocation-id>
<history>
<date date-type="received">
<day>19</day>
<month>1</month>
<year>2004</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>8</month>
<year>2004</year>
</date>
</history>
<permissions>
<copyright-statement>© Springer Science+Business Media, Inc. 2005</copyright-statement>
<license>
<license-p>This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p>
</license>
</permissions>
<abstract id="Abs1">
<p>Marine sponges have been considered as a gold mine during the past 50 years, with respect to the diversity of their secondary metabolites. The biological effects of new metabolites from sponges have been reported in hundreds of scientific papers, and they are reviewed here. Sponges have the potential to provide future drugs against important diseases, such as cancer, a range of viral diseases, malaria, and inflammations. Although the molecular mode of action of most metabolites is still unclear, for a substantial number of compounds the mechanisms by which they interfere with the pathogenesis of a wide range of diseases have been reported. This knowledge is one of the key factors necessary to transform bioactive compounds into medicines. Sponges produce a plethora of chemical compounds with widely varying carbon skeletons, which have been found to interfere with pathogenesis at many different points. The fact that a particular disease can be fought at different points increases the chance of developing selective drugs for specific targets.</p>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>sponge medicine</kwd>
<kwd>natural product</kwd>
<kwd>cancer</kwd>
<kwd>inflammation</kwd>
<kwd>virus</kwd>
</kwd-group>
<custom-meta-group>
<custom-meta>
<meta-name>issue-copyright-statement</meta-name>
<meta-value>© Springer Science+Business Media, Inc. 2005</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body>
<sec id="Sec1" sec-type="introduction">
<title>I
<sc>NTRODUCTION</sc>
</title>
<p>The relationship between sponges and medicines goes back to Alexandrian physicians and was thoroughly describes by the Roman historian Plinius. Physicians used sponges that were saturated with iodine to stimulate coagulation of the blood, or with bioactive plant extracts to anesthetize patients. Sponges were soaked with pure wine and put on the left part of the chest in case of heartaches and soaked in urine to treat bites of poisonous animals. Plinius recommended the use of sponges against sunstrokes, and they were used against all kinds of wounds, bone fractures, dropsy, stomach aches, infectious diseases, and testicular tumors (
<xref ref-type="bibr" rid="CR76">Hofrichter and Sidri, 2001</xref>
), or even as implants after breast operations (
<xref ref-type="bibr" rid="CR8">Arndt, 1938</xref>
). At least since the 18th century, Russian, Ukrainian, and Polish physicians have used a freshwater sponge they call Badiaga (Figure 
<xref rid="Fig1" ref-type="fig">1</xref>
) for the treatment of patients (
<xref ref-type="bibr" rid="CR134">Nozeman, 1788</xref>
). The dry powder of this sponge is rubbed on the chest or back of patients with lung diseases or on the sore places in cases of foot and leg aches (such as rheumatism (
<xref ref-type="bibr" rid="CR164">Schroder, 1942</xref>
).
<xref ref-type="bibr" rid="CR135">Oficjalski (1937)</xref>
discovered that Badiaga is not really one sponge, but mixtures of several freshwater sponges that differ depending on the region. In Poland it consisted of powder of
<italic>Euspongilla lacustris</italic>
,
<italic>Ephydatia fluviatilis</italic>
, and
<italic>Meyenia muelleri</italic>
, while the Russian Badiaga was a mixture of
<italic>Euspongilla lacustris</italic>
,
<italic>Ephydatia fluviatilis</italic>
,
<italic>Spongilla fragilis</italic>
, and
<italic>Carterius stepanowi.</italic>
He suggested that the high iodine concentration in all sponge species gives rise to the wholesome effect of Badiaga. At present Stodal, syrup containing roasted
<italic>Spongia officinalis</italic>
, is used for homeopathic treatment of dry and asthmatic cough in the Western world (
<xref ref-type="bibr" rid="CR175">Stodal, 2003</xref>
).
<fig id="Fig1">
<label>Figure 1</label>
<caption>
<p>Examples of homeopathic drugs based on sponge extracts currently in use (Badiaga and Stodal syrup).</p>
</caption>
<graphic xlink:href="10126_2004_405_f1" id="MO8"></graphic>
</fig>
</p>
<p>Pharmaceutical interest in sponges was aroused in the early 1950s by the discovery of a nucleosides spongothymidine and spongouridine in the marine sponge
<italic>Cryptotethia crypta</italic>
(
<xref ref-type="bibr" rid="CR14">Bergmann and Feeney, 1950</xref>
,
<xref ref-type="bibr" rid="CR15">1951)</xref>
. These nucleosides were the basis for the synthesis of Ara-C, the first marine-derived anticancer agent, and the antiviral drug Ara-A (
<xref ref-type="bibr" rid="CR147">Proksch et al., 2002</xref>
). Ara-C is currently used in the routine treatment of patients with leukemia and lymphoma. One of its fluorinated derivatives has also been approved for use in patients with pancreatic, breast, bladder, and lung cancer (
<xref ref-type="bibr" rid="CR166">Schwartsmann, 2000</xref>
). At the same time it was revealed that certain lipid components such as fatty acids, sterols and other unsaponifiable compounds occur in lower invertebrates in a diversity far greater than that encountered among animals of higher organization (
<xref ref-type="bibr" rid="CR16">Bergmann and Swift, 1951</xref>
). These early promises have now been substantiated by an overwhelming number of bioactive compounds that have been discovered in marine organisms. More than 15,000 marine products have been described thus for (
<xref ref-type="bibr" rid="CR113">MarinLit, 1999</xref>
;
<xref ref-type="bibr" rid="CR54">Faulkner, 2000</xref>
,
<xref ref-type="bibr" rid="CR55">2001</xref>
,
<xref ref-type="bibr" rid="CR56">2002)</xref>
. Sponges, in particular, are responsible for more than 5300 different products, and every year hundreds of new compounds are being discovered (
<xref ref-type="bibr" rid="CR54">Faulkner 2000</xref>
,
<xref ref-type="bibr" rid="CR55">2001</xref>
,
<xref ref-type="bibr" rid="CR56">2002)</xref>
.</p>
<p>Most bioactive compounds from sponges can be classified as antiinflammatory, antitumor, immunosuppressive or neurosuppressive, antiviral, antimalarial, antibiotic, or antifouling. The chemical diversity of sponge products is remarkable. In addition to the unusual nucleosides, bioactive terpenes, sterols, cyclic peptides, alkaloids, fatty acids, peroxides, and amino acid derivatives (which are frequently halogenated) have been described from sponges (Figure 
<xref rid="Fig2" ref-type="fig">2</xref>
).
<fig id="Fig2">
<label>Figure 2</label>
<caption>
<p>An illustration of the chemical diversity of sponge-derived molecules.
<bold>a:</bold>
Xestospongin C (
<italic>Xestospongia</italic>
sp. / macrocyclic bis-oxaquinolizidine.
<bold>b:</bold>
Spongothymidine (
<italic>Cryptotethia crypta /</italic>
unusual nucleoside).
<bold>c:</bold>
discorhabdin D (
<italic>Latrunculia brevis; Prianos</italic>
sp. / fused pyrrolophenanthroline alkaloid.
<bold>d:</bold>
Contignasterol (
<italic>Petrosia contignata /</italic>
oxygenated sterol).
<bold>e:</bold>
Jaspamide (
<italic>Hemiastrella minor /</italic>
macrocyclic lactam/lactone).
<bold>f:</bold>
agelasphin (
<italic>Agelas mauritianus /</italic>
α-galactosylceramide).</p>
</caption>
<graphic xlink:href="10126_2004_405_f2" id="MO9"></graphic>
</fig>
</p>
<p>For this review we have surveyed the discoveries of products derived from marine sponges up to now, and attempted to show the variety of potential medical applications of metabolites from sponges and the mechanisms by which they interfere with the pathogenesis of human diseases. This knowledge is a prerequisite for the development of a drug from a bioactive compound. For example, many secondary metabolites inhibit growth of cancer cell lines, but this does not imply that they will be suitable as a medicine against cancer, because they may exhibit important side effects. The following sections summarize compounds by disease type and describe their mode of action, and discuss the reasons why sponges would produce these metabolites.</p>
</sec>
<sec id="Sec2">
<title>S
<sc>PONGE </sc>
P
<sc>RODUCTS</sc>
</title>
<sec id="Sec3">
<title>Antiinflammatory Compounds</title>
<p>Acute inflammations in the human body can result from microbial infection, physical damage, or chemical agents. The body reacts by changing the blood flow, increasing the permeability of blood vessels, and allowing the escape of cells from the blood into the tissues (Tan et al., 1999). Chronic inflammation of the skin or joints may severely damage the body if it leads to psoriasis or rheumatic arthritis (
<xref ref-type="bibr" rid="CR145">Pope et at., 1999</xref>
). Sponges have proved to be an interesting source of antiinflammatory compounds (Table 
<xref rid="Tab1" ref-type="table">1</xref>
).
<table-wrap id="Tab1">
<label>Table 1</label>
<caption>
<p>Examples of Antiinflammatory Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Mode of action</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Manoalide</td>
<td align="left">Cyclohexane sesterterpenoid</td>
<td align="left">
<italic>Luffariella variabilis</italic>
/Dictyoceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR13">Bennet et al., 1987</xref>
</td>
</tr>
<tr>
<td align="left">Dysidotronic acid</td>
<td align="left">Drimane sesquiterpenoid</td>
<td align="left">
<italic>Dysidea</italic>
sp./Dendroceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR69">Giannini et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Ircinin-1 and -2</td>
<td align="left">Acyclic sesterterpenoid</td>
<td align="left">
<italic>Ircinia oros</italic>
/Dictyoceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR33">Ciminoe et al., 1972</xref>
</td>
</tr>
<tr>
<td align="left">Petrosaspongiolides M-R</td>
<td align="left">Cheilantane sesterterpenoid</td>
<td align="left">
<italic>Petrosaspongia nigra/</italic>
Dictyoceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR151">Randazzo et al., 1998a</xref>
</td>
</tr>
<tr>
<td align="left">Spongidines A-D</td>
<td align="left">Pyridinium alkaloid</td>
<td align="left">
<italic>Spongia</italic>
sp./Dictyoceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR43">De Marino et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Topsentin</td>
<td align="left">Bis-indole alkaloid</td>
<td align="left">
<italic>Topsentia genitrix</italic>
/Halichondrida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR85">Jacobs et al., 1994</xref>
</td>
</tr>
<tr>
<td align="left">Scalaradial</td>
<td align="left">Scalarane sesterterpene</td>
<td align="left">
<italic>Cacospongia scalaris</italic>
/Dictyoceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR41">De Carvalho and Jacobs, 1991</xref>
</td>
</tr>
<tr>
<td align="left">Cacospongionolide B</td>
<td align="left">Sesterterpene lactone</td>
<td align="left">
<italic>Fasciospongia cavernosa</italic>
/Dictyoceratida</td>
<td align="left">Phospholipase A
<sub>2</sub>
inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR67">Garcia Pastor et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Jaspaquinol</td>
<td align="left">Diterpene benzenoid</td>
<td align="left">
<italic>Jaspis splendens</italic>
/Astrophorida</td>
<td align="left">Lipoxygenase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR30">Carroll et al., 2001</xref>
</td>
</tr>
<tr>
<td align="left">Subersic acid</td>
<td align="left">Diterpene benzenoid</td>
<td align="left">
<italic>Suberea</italic>
sp./Verongida</td>
<td align="left">Lipoxygenase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR30">Carroll et al., 2001</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
<p>Manoalide, one of the first sesterterpenoids to be isolated from a marine sponge (
<italic>Luffariella variabilis</italic>
),
<italic>was</italic>
found to be an antibiotic (
<xref ref-type="bibr" rid="CR46">De Silva and Scheuer, 1980</xref>
) and an analgesic (
<xref ref-type="bibr" rid="CR117">Mayer and Jacobs, 1988</xref>
). In addition, its antiinflammatory properties have been studied extensively (
<xref ref-type="bibr" rid="CR13">Bennet et al., 1987</xref>
). The antiinflammatory action is based on the irreversible inhibition of the release of arachidonic acid from membrane phospholipids by preventing the enzyme phospholipase A
<sub>2</sub>
from binding to the membranes (
<xref ref-type="bibr" rid="CR70">Glaser et al., 1989</xref>
). A rise in the intracellular arachidonic acid concentration would lead to upregulation of the synthesis of inflammation mediators as prostaglandins and leukotrienes (Figure 
<xref rid="Fig3" ref-type="fig">3</xref>
). Phospholipase A
<sub>2</sub>
inhibition has been recorded for many sesterterpenes from sponges of the order Dictyoceratida, but also for bis-indole alkaloids such as topsentin (
<xref ref-type="bibr" rid="CR85">Jacobs et al., 1994</xref>
). The mechanism by which they affect the inflammation process is different from commonly used nonsteroidal antiinflammatory drugs. Only a few sponge-derived terpenoids have been found to inhibit lipoxygenase, another enzyme that is involved in the inflammatory response (
<xref ref-type="bibr" rid="CR30">Carroll et al., 2001</xref>
).
<fig id="Fig3">
<label>Figure 3</label>
<caption>
<p>Inflammatory cascade inside the cell. Phospholipase A
<sub>2</sub>
(PLA
<sub>2</sub>
) catalyzes the release of membrane-bound arachidonic acid (AA) to free arachidonic acid. Arachidonic acid is converted to leukotrienes and prostaglandins by lipoxygenase (LOX) and cyclooxygenase-2 (COX-2), respectively. Sponge-derived antiinflammatory molecules are mainly inhibitors of PLA
<sub>2</sub>
or LOX, while nonsteroidal antiinflammatory drugs inhibit COX-2, but also the constitutive COX-1.</p>
</caption>
<graphic xlink:href="10126_2004_405_f3" id="MO10"></graphic>
</fig>
</p>
<p>The antiinflammatory sponge products are selective inhibitors of specific enzymes of a range of diseases, like psoriasis or rheumatic arthritis. The currently used nonsteroidal antiinflammatory drugs often fail to control the disease and present important side effects such as risk of gastrointestinal bleeding and renal complications (
<xref ref-type="bibr" rid="CR45">De Rosa, 2002</xref>
). These are caused by unselective inhibition of cyclooxygenases, some of which are also involved in the promotion of the production of the natural mucus that protects the gastrointestinal tract (
<xref ref-type="bibr" rid="CR18">Bjarnason et al., 1993</xref>
).</p>
</sec>
<sec id="Sec4">
<title>Antitumor Compounds</title>
<p>A number of isolated sponge compounds are inhibitors of protein kinase C (PKC). PKC inhibitors have attracted interest worldwide, as there is evidence that too high levels of PKC enzyme are involved both in the pathogenesis of arthritis and psoriasis (owing to regulation of phospholipase A
<sub>2</sub>
activity), and in tumor development (
<xref ref-type="bibr" rid="CR22">Bradshaw et al., 1993</xref>
;
<xref ref-type="bibr" rid="CR195">Yoshiji et al., 1999</xref>
). PKC is believed to be the receptor protein of tumor-promoting phorbol esters, and PKC inhibitors prevent binding of carcinosarcoma cells to the endothelium (
<xref ref-type="bibr" rid="CR108">B. Liu et al., 1991</xref>
). Glycosylation of the receptors, and especially the presence of fucose residues, plays an important role in the binding of carcinosarcoma cells and leukocytes to the receptors in the endothelium (
<xref ref-type="bibr" rid="CR173">Springer and Lasky, 1991</xref>
).</p>
<p>Fucosyltransferase inhibitors, such as the octa- and nonaprenylhydroquinone sulfates that were isolated from a
<italic>Sarcotragus</italic>
sp. (
<xref ref-type="bibr" rid="CR190">Wakimoto et al., 1999</xref>
), may therefore be promising candidates for controlling inflammatory processes such as arthritis or for combating tumor growth.</p>
<p>In addition to PKC inhibitors and fucosyl transferase inhibitors, numerous anticancer molecules with a different mode of action have been discovered in marine sponges (Table 
<xref rid="Tab2" ref-type="table">2</xref>
). These compounds can be divided in 3 classes:
<table-wrap id="Tab2">
<label>Table 2</label>
<caption>
<p>Examples of Antitumor Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Mode of action</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">BRS1</td>
<td align="left">Diamino-dihydroxy polyunsaturated lipid</td>
<td align="left">Calcareous sponge/?</td>
<td align="left">Protein kinase C inhibitor
<sup>a</sup>
</td>
<td align="left">
<xref ref-type="bibr" rid="CR193">Willis and De Vries, 1997</xref>
</td>
</tr>
<tr>
<td align="left">Isoaaptamine</td>
<td align="left">Benzonaphthyridine alkaloid</td>
<td align="left">
<italic>Aaptos aaptos</italic>
/Hadromerida</td>
<td align="left">Protein kinase C inhibitor
<sup>a</sup>
</td>
<td align="left">
<xref ref-type="bibr" rid="CR57">Fedoreev et al., 1989</xref>
</td>
</tr>
<tr>
<td align="left">Debromohymenialdisine</td>
<td align="left">Pyrrole-guanidine alkaloid, prenylhydroquinone derivative</td>
<td align="left">
<italic>Hymeniacidonaldis</italic>
/Halichondrida</td>
<td align="left">Protein kinase C inhibitor
<sup>a</sup>
</td>
<td align="left">
<xref ref-type="bibr" rid="CR92">Kitagawa et al., 1983</xref>
</td>
</tr>
<tr>
<td align="left"></td>
<td align="left"></td>
<td align="left">
<italic>Sarcotragus</italic>
sp./Dictyoceratida</td>
<td align="left">A1, 3-fucosyltransferase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR190">Wakimoto et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Adociasulfates</td>
<td align="left">Triterpenoid hydroquinones</td>
<td align="left">
<italic>Haliclona (aka Adocia)</italic>
sp./Haplosclerida</td>
<td align="left">Kinesin motor protein inhibitors</td>
<td align="left">
<xref ref-type="bibr" rid="CR19">Blackburn et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Discodermolide</td>
<td align="left">Linear tetraene lactone</td>
<td align="left">
<italic>Discodermia dissolute</italic>
/Lithistida</td>
<td align="left">Stabilization of microtubules</td>
<td align="left">
<xref ref-type="bibr" rid="CR181">Ter Haar et al., 1996</xref>
</td>
</tr>
<tr>
<td align="left">Laulimalide</td>
<td align="left">Macrocyclic lactone</td>
<td align="left">
<italic>Cacospongia mycofljiensis</italic>
/Dictyoceratida</td>
<td align="left">Stabilization of microtubules</td>
<td align="left">
<xref ref-type="bibr" rid="CR122">Mooberry et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Peloruside A</td>
<td align="left">Macrocyclic lactone</td>
<td align="left">
<italic>Mycdle hentschett</italic>
/Poecilosclerida</td>
<td align="left">Stabilization of microtubules</td>
<td align="left">
<xref ref-type="bibr" rid="CR79">Hood et al., 2002</xref>
</td>
</tr>
<tr>
<td align="left">Hemiasterlin</td>
<td align="left">Unusual tripeptide</td>
<td align="left">
<italic>Auletta</italic>
sp./Halichondrida</td>
<td align="left">Stabilization of microtubules</td>
<td align="left">
<xref ref-type="bibr" rid="CR2">Anderson et al., 1997</xref>
</td>
</tr>
<tr>
<td align="left">Dictyostatin</td>
<td align="left">Macrocyclic lactone</td>
<td align="left">
<italic>Corallistidae</italic>
sp./Lithistida</td>
<td align="left">Stabilization of microtubules</td>
<td align="left">
<xref ref-type="bibr" rid="CR84">Isbrucker et al., 2003</xref>
</td>
</tr>
<tr>
<td align="left">Spongistatin 1</td>
<td align="left">Bis(spiroacetal) macrolide</td>
<td align="left">
<italic>Spongia</italic>
sp./Dictyoceratida</td>
<td align="left">Tubulin polymerisation inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR10">Bai et al., 1993</xref>
</td>
</tr>
<tr>
<td align="left">Halichondrin B</td>
<td align="left">Polyether macrolide</td>
<td align="left">e.g.,
<italic>Halichondria okadai</italic>
/Halichondrida</td>
<td align="left">Tubulin polymerisation inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR73">Hirata and Uemura, 1986</xref>
;
<xref ref-type="bibr" rid="CR9">Bai et al., 1991</xref>
</td>
</tr>
<tr>
<td align="left">Arenastatin A</td>
<td align="left">Macrocyclic lactan/lactone</td>
<td align="left">
<italic>Dysidea arenaria</italic>
/Dendroceratida</td>
<td align="left">Tubulin polymerisation inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR97">Koiso et al., 1996</xref>
</td>
</tr>
<tr>
<td align="left">Latrunculin A</td>
<td align="left">Thiazole macrolide</td>
<td align="left">
<italic>Latrunculia magnified</italic>
/Poecilosclerida</td>
<td align="left">Actin-depolymerisation</td>
<td align="left">
<xref ref-type="bibr" rid="CR88">Kashman et al., 1980</xref>
<xref ref-type="bibr" rid="CR36">Coue et al., 1987</xref>
</td>
</tr>
<tr>
<td align="left">Swinholide A</td>
<td align="left">Macrocyclic lactone</td>
<td align="left">
<italic>Theonella swinhoei/</italic>
Lithistida</td>
<td align="left">Actin-depolymerization</td>
<td align="left">
<xref ref-type="bibr" rid="CR24">Bubb et al., 1995</xref>
</td>
</tr>
<tr>
<td align="left">Mycalolide B</td>
<td align="left">Oxazole macrolide</td>
<td align="left">
<italic>Mycale</italic>
sp./Poecilosclerida</td>
<td align="left">Actin-depolymerization</td>
<td align="left">
<xref ref-type="bibr" rid="CR62">Fusetani et al., 1989</xref>
<xref ref-type="bibr" rid="CR159">Saito et al., 1994</xref>
</td>
</tr>
<tr>
<td align="left">Jaspamide</td>
<td align="left">Macrocyclic lactam/lactone</td>
<td align="left">
<italic>Hemiastrella minor</italic>
/Hadromerida</td>
<td align="left">Actin filament stabilizer</td>
<td align="left">
<xref ref-type="bibr" rid="CR52">Fabian et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Fascaplysin</td>
<td align="left">Bisindole alkaloid</td>
<td align="left">
<italic>Fascaplysinopsis </italic>
sp./Dictyoceratida</td>
<td align="left">Cyclin-dependent kinase 4 inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR172">Soni et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Spongiacidin B</td>
<td align="left">Pyrrole alkaloid</td>
<td align="left">
<italic>Hymeniacidon </italic>
sp. / Halichondrida</td>
<td align="left">Cyclin-dependent kinase 4 inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR83">Inaba et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Mycalamide A and B</td>
<td align="left">Polyether amide (pederin-like)</td>
<td align="left">
<italic>Mycale </italic>
sp./Poecilosclerida</td>
<td align="left">Protein synthesis inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR27">Burres and Clement, 1989</xref>
</td>
</tr>
<tr>
<td align="left">Girodazole</td>
<td align="left">Imidazole alkaloid</td>
<td align="left">
<italic>Cymbastela cantharella</italic>
/Halichondrida</td>
<td align="left">Protein synthesis inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR1">Ahond et al., 1988</xref>
;
<xref ref-type="bibr" rid="CR34">Colson et al., 1992</xref>
</td>
</tr>
<tr>
<td align="left">Aragusterol A</td>
<td align="left">Sterol</td>
<td align="left">
<italic>Xestospongia </italic>
sp./Haplosclerida</td>
<td align="left">Protein synthesis inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR82">Iguchi et al., 1993</xref>
;
<xref ref-type="bibr" rid="CR60">Fukuoka et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Neoamphimedine</td>
<td align="left">Pyridoacridine alkaloid</td>
<td align="left">
<italic>Xestospongia </italic>
cf.
<italic>carbonaria/</italic>
Haplosclerida</td>
<td align="left">Topoisomerase II inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR42">De Guzman et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Elenic acid</td>
<td align="left">Alkylphenol</td>
<td align="left">
<italic>Plakinastrella </italic>
sp./Homosclerophorida</td>
<td align="left">Topoisomerase II inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR87">Juagdan et al., 1995</xref>
</td>
</tr>
<tr>
<td align="left">Naamine D</td>
<td align="left">Imidazole alkaloid</td>
<td align="left">
<italic>Leucetta </italic>
cf.
<italic>chagosensis</italic>
/Calcinea</td>
<td align="left">Nitric oxide synthetase inhibitor
<sup>b</sup>
</td>
<td align="left">
<xref ref-type="bibr" rid="CR49">Dunbar et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Agelasphin (KRN7000)</td>
<td align="left">α-Galactosylceramide</td>
<td align="left">
<italic>Agelas mauritianus </italic>
/Agelasida</td>
<td align="left">NKT cell activator</td>
<td align="left">
<xref ref-type="bibr" rid="CR168">Shimosaka, 2002</xref>
</td>
</tr>
<tr>
<td align="left">Agosterol A</td>
<td align="left">Sterol</td>
<td align="left">
<italic>Spongia </italic>
sp./Dictyoceratida</td>
<td align="left">Reverses drug resistancy of dancer cells</td>
<td align="left">
<xref ref-type="bibr" rid="CR6">Aoki et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Salicylihalamide A</td>
<td align="left">Salicylate macrolide</td>
<td align="left">
<italic>Haliclona </italic>
sp./Haplosclerida</td>
<td align="left">v-ATPase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR51">Erickson et al., 1997</xref>
</td>
</tr>
<tr>
<td align="left">Chondropsin A and B</td>
<td align="left">Macrolide lactam</td>
<td align="left">
<italic>Chondropsis </italic>
sp./Poecilosclerida</td>
<td align="left">v-ATPase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR29">Cantrell et al., 2000</xref>
;
<xref ref-type="bibr" rid="CR21">Bowman et al., 2003</xref>
</td>
</tr>
<tr>
<td align="left">6-Hydroximino-4-en-3-one steroids</td>
<td align="left">Oximated steroid</td>
<td align="left">
<italic>Cinachyrella </italic>
sp./Spirophorida</td>
<td align="left">Aromatase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR77">Holland et al., 1992</xref>
</td>
</tr>
<tr>
<td align="left">Crambescidins 1-4</td>
<td align="left">Pentacyclic guanidine derivative</td>
<td align="left">
<italic>Crambe crambe</italic>
/Poecilosclerida</td>
<td align="left">Ca
<sup>2+</sup>
/channel blocker</td>
<td align="left">
<xref ref-type="bibr" rid="CR86">Jares-Erijman et al., 1991</xref>
;
<xref ref-type="bibr" rid="CR17">Berlinck et al., 1993</xref>
</td>
</tr>
<tr>
<td align="left">Haligramides A and B</td>
<td align="left">Cyclic peptide</td>
<td align="left">
<italic>Haliclona nigra</italic>
/Haplosclerida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR153">Rashid et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Discorhabdin D</td>
<td align="left">Fused pyrrolophenanthroline alkaloid</td>
<td align="left">
<italic>Latrunculia brevis</italic>
/Poecilosclerida;
<italic>Prianos </italic>
sp./Haplosclerida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR140">Perry et al., 1988</xref>
</td>
</tr>
<tr>
<td align="left">Callystatin A</td>
<td align="left">Polyketide</td>
<td align="left">
<italic>Callyspongia truncata</italic>
/Haplosclerida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR95">Kobayashi et al., 1997</xref>
</td>
</tr>
<tr>
<td align="left">Tedanolide</td>
<td align="left">Macrocyclic lactone</td>
<td align="left">
<italic>Tedania ignis</italic>
/Poecilosclerida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR163">Schmitz et al., 1984</xref>
</td>
</tr>
<tr>
<td align="left">Glaciasterols A and B</td>
<td align="left">9, 11-Secosterol</td>
<td align="left">
<italic>Aplysilla glacialis/</italic>
Dendroceratida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR144">Pika et al., 1992</xref>
</td>
</tr>
<tr>
<td align="left">Axinellins A and B</td>
<td align="left">Cyclic peptide</td>
<td align="left">
<italic>Axinella carter!</italic>
/Halichondrida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR152">Randazzo et al., 1998b</xref>
</td>
</tr>
<tr>
<td align="left">Incrustasterols A and B</td>
<td align="left">Sterol</td>
<td align="left">
<italic>Dysidea incrustans</italic>
/Dendroceratida</td>
<td align="left">Unknown</td>
<td align="left">
<xref ref-type="bibr" rid="CR31">Casapullo et al., 1995</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>
<sup>a</sup>
Also has antiinflammatory activity.</p>
<p>
<sup>b</sup>
Also has immunosuppressive activity.</p>
</table-wrap-foot>
</table-wrap>
</p>
<p>(1) nonspecific inhibitors of cell growth; (2) specific inhibitors of cancer cells; and (3) inhibitors of cancer cells of a certain type of cancer (as the aforementioned PKC inhibitors).</p>
<p>Many nonspecific cell growth inhibitors have been discovered in sponges. They are valuable for treating cancer under certain conditions, but they also affect the division of healthy cells. Therefore, their applications are limited, depending on their specific characteristics. The cytoskeleton is an interesting target for cancer therapy, as the microtubules and microfilaments are involved in cellular organization during cell division. A number of adociasulfates (triterpenoid hydroquinones) from a
<italic>Haticlona</italic>
sp. were the first inhibitors of the kinesin motor protein to be discovered. These toxins are believed to inhibit the protein by binding to the microtubule binding site, “locking up” the protein’s motor function, and thereby blocking cell division (
<xref ref-type="bibr" rid="CR19">Blackburn et al., 1999</xref>
). In addition to these triterpenoid hydroquinones, a number of potent microtubule-interfering compounds have been discovered in marine sponges, such as halichondrin B (
<xref ref-type="bibr" rid="CR9">Bai et al., 1991</xref>
), spongistatin (
<xref ref-type="bibr" rid="CR10">Bai et al., 1993</xref>
), discodermolide (
<xref ref-type="bibr" rid="CR181">Ter Haar et al., 1996</xref>
), laulimalide (
<xref ref-type="bibr" rid="CR122">Moobeny et al., 1999</xref>
), peloruside A (
<xref ref-type="bibr" rid="CR79">Hood et al., 2002</xref>
), and dictyostatin (
<xref ref-type="bibr" rid="CR84">Isbrucker et al., 2003</xref>
). Other metabolites, such as latrunculin A from
<italic>Latrunculia magnifica</italic>
(
<xref ref-type="bibr" rid="CR36">Coue et al., 1987</xref>
) and swinholide A from
<italic>Theonella swinhoei</italic>
(Bubb et al., 1998), disrupt the polymerization of actin. Actin which is the key element of the microfilaments, and it can block many cellular processes including cell division. Spongiacidin B (
<xref ref-type="bibr" rid="CR83">Inaba et al., 1998</xref>
) and fascaplysin (
<xref ref-type="bibr" rid="CR172">Soni et al., 2000</xref>
) are examples of sponge-derived metabolites that inhibit cell division by inhibition of cyclin-dependent kinase 4, which leads to arrest of cells in the G1 phase. Other metabolites, such as mycalamide (
<xref ref-type="bibr" rid="CR27">Burres and Clement, 1989</xref>
) and aragusterol (
<xref ref-type="bibr" rid="CR60">Fukuoka et al., 2000</xref>
), disturb cell division by inhibition of protein synthesis. Neoamphimedine (
<xref ref-type="bibr" rid="CR42">De Guzman et al., 1999</xref>
) and elenic acid (
<xref ref-type="bibr" rid="CR87">Juagdan et al., 1995</xref>
) inhibit the development of tumors by blocking topoisomerase II, the nuclear enzyme which makes transient DNA breaks that are required for replication (
<xref ref-type="bibr" rid="CR109">L.F. Liu and Chen, 1994</xref>
).</p>
<p>Nitric oxide synthetase inhibitors, such as the imidazole alkaloid Na amine D that was isolated from the calcareous sponge
<italic>Leucetta</italic>
cf.
<italic>chagosensis</italic>
(
<xref ref-type="bibr" rid="CR49">Dunbar et al., 2000</xref>
), are not involved in growth inhibition of cancer cells, but may prevent events in the early phases of tumorigenesis. Nitric oxide could participate in the tumorigenesis by mediating DNA damage and support tumor progression through the induction of angiogenesis (
<xref ref-type="bibr" rid="CR103">Lala and Orucevic, 1998</xref>
). However, inhibition of nitric oxide synthetase may also affect other physiologic processes in which nitric oxide is involved, such as intracellular or transcellular messaging, and it is involved in regulation of the immunogenic respons by T lymphocytes. Agelasphin (KRN7000) from
<italic>Agelas mauritianus</italic>
(
<xref ref-type="bibr" rid="CR94">E. Kobayashi et al., 1995</xref>
) has been found to stimulate the immune system by activation of dendritic and natural killer T (NKT) cells. The NKT cell level is lower in the blood of patients with cancer or autoimmune disease, such as type 1 diabetes (
<xref ref-type="bibr" rid="CR168">Shimosaka, 2002</xref>
), and in mice it was shown that tumors could be rejected by stimulation of the immune system by agelasphin (
<xref ref-type="bibr" rid="CR194">Yamaguchi et al., 1996</xref>
).</p>
<p>The activity of other compounds is more specific toward tumor cells. Multidrug resistance in human carcinoma cells caused by overexpression of two kinds of membrane glycoproteins is reversed by agosterol A from the marine sponge
<italic>Spongia</italic>
sp. It has been suggested that an altered cytosolic pH plays a role in drug resistance. Vascular (H
<sup>+</sup>
) ATPase (v-ATPase) is an enzyme involved in many cellular processes that are often upregulated in cancer cells, such as acidic vesicular organelle formation, which is a response to radiation injury or manipulation of the pH to decrease entry of chemotherapeutics into the cells (
<xref ref-type="bibr" rid="CR114">Martinez-Zaguilan et al., 1999</xref>
). Salicylihamide A was isolated from a
<italic>Haliclona</italic>
sp. as a selective inhibitor of v-ATPase and has been shown to be 60-fold more cytotoxic to certain cancer cells than to their normal noncancerous counterparts (
<xref ref-type="bibr" rid="CR51">Erickson et al., 1997</xref>
). The first natural 6-hydroximino-4-en-3-one steroids were isolated from
<italic>Cinachyrella</italic>
spp. (
<xref ref-type="bibr" rid="CR155">Rodriguez et al., 1997</xref>
) and are examples of molecules that can be deployed against a specific type of cancer. They displayed high affinity to aromatase (
<xref ref-type="bibr" rid="CR77">Holland et al., 1992</xref>
), which is the rate-limiting enzyme that catalyzes the conversion of androgens to estrogens (Figure 
<xref rid="Fig4" ref-type="fig">4</xref>
). Blockade of this step allows treatment of hormone-sensitive breast cancer that is dependent on estrogen (
<xref ref-type="bibr" rid="CR110">Lonning et al., 2003</xref>
). A peculiar fact about the 6-hydroximi no-4-en-3-one steroids is that they were chemically synthesized before they were even discovered in nature.
<fig id="Fig4">
<label>Figure 4</label>
<caption>
<p>Inhibition of breast cancer by
<italic>Cinachyrella</italic>
sp. steroids. Aromatase is the key enzyme in the formation of the estrogens estrone (E
<sub>1</sub>
) and estradiol (E
<sub>2</sub>
). It catalyzes the final steps, from androstenedione (A) to estron and from testosterone (T) to estradiol, in the estrogen pathway. Estrogen conversion can occur in the blood, in normal breast tissue, as well as in breast tumor tissue (adapted from
<xref ref-type="bibr" rid="CR68">Geisler, 2003</xref>
). The 6-hydroximino-4-en-3-one steroids from
<italic>Cinachyrella</italic>
sp. are inhibitors of aromatase. The inhibition of aromatase in the tumor tissue is not shown to maintain the clarity of the illustration.</p>
</caption>
<graphic xlink:href="10126_2004_405_f4" id="MO11"></graphic>
</fig>
</p>
<p>In addition, many more compounds that displayed growth inhibition activity of tumor cell lines have been isolated (Table 
<xref rid="Tab2" ref-type="table">2</xref>
), although their exact effects are still unclear. Discorhabdin D (
<xref ref-type="bibr" rid="CR140">Perry et al., 1988</xref>
), chondropsin A and B (
<xref ref-type="bibr" rid="CR29">Cantrell et al., 2000</xref>
), haligramides A and B (
<xref ref-type="bibr" rid="CR153">Rashid et al., 2000</xref>
), and glaciasterols A and B (
<xref ref-type="bibr" rid="CR144">Pika et al., 1992</xref>
) are only a few examples of these molecules.</p>
</sec>
<sec id="Sec5">
<title>Immunosuppressive Compounds</title>
<p>In addition to their potential for treatment of cancer, nitric oxide synthetase inhibitors downregulate T-cells are, suppressing the immune system, and they diminish the fierceness of migraine attacks (
<xref ref-type="bibr" rid="CR71">Griffith and Gross, 1996</xref>
). Immune system suppression is desired in cases of hypersensitivity to certain antigens (e.g., allergies) or organ transplantations. Patients who receive a donor organ need life-long medication to prevent rejection by the immune system, and for that reason it is extremely important that these medicines are very specific suppressors. Therefore there is a continuous demand for new immunosuppressives. A number of new molecules with immunosuppressive activity, which interfere at different points of the immune response have been discovered in marine sponges (Table 
<xref rid="Tab3" ref-type="table">3</xref>
; Figure 
<xref rid="Fig5" ref-type="fig">5</xref>
).
<table-wrap id="Tab3">
<label>Table 3</label>
<caption>
<p>Examples of Immunosuppressive Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Mode of action</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Simplexides</td>
<td align="left">Glycolipid</td>
<td align="left">
<italic>Plakortis simplex</italic>
/Homosclerophorida</td>
<td align="left">Inhibitor of T-cell proliferation</td>
<td align="left">
<xref ref-type="bibr" rid="CR35">Costantino et al.,1999</xref>
</td>
</tr>
<tr>
<td align="left">Polyoxygenated sterols</td>
<td align="left">Sterol</td>
<td align="left">
<italic>Dysidea</italic>
sp./Dendroceratida</td>
<td align="left">IL-8 inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR107">Leone et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Contignasterol</td>
<td align="left">Oxygenated sterol</td>
<td align="left">
<italic>Petrosia contignata</italic>
/Haplosclerida</td>
<td align="left">Histamine release inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR179">Takei et al., 1994</xref>
;
<xref ref-type="bibr" rid="CR23">Bramley et al., 1995</xref>
</td>
</tr>
<tr>
<td align="left">Xestobergsterols A and B</td>
<td align="left">Pentacyclic sterol</td>
<td align="left">
<italic>Xestosponga berquistia</italic>
/Haplosclerida</td>
<td align="left">Histamine release inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR169">Shoji et al., 1992</xref>
</td>
</tr>
<tr>
<td align="left">Taurodispacamide A</td>
<td align="left">Pyrrole-imidazole alkaloid</td>
<td align="left">
<italic>Agelas oroides</italic>
/Agelasida</td>
<td align="left">IL-2 inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR53">Fattorusso and Taglialatela-Scafati, 2000</xref>
</td>
</tr>
<tr>
<td align="left">Pateamine A</td>
<td align="left">Thiazole macrolide</td>
<td align="left">
<italic>Mycale</italic>
sp./Poecilosclerida</td>
<td align="left">IL-2 inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR133">Northcote et al., 1991</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="Fig5">
<label>Figure 5</label>
<caption>
<p>Simplified representation of the immune respons after capture of an antigen by macrophages (M). Both macrophages, but especially T-helper cells (T-help), secrete many interleukins (IL-x) or macrophage activation factor (MAP), to trigger the primary immune response via neutrophils (N), or the secondary immune respons by activating resting T cells (T-rest) and B cells (B). Activated B cells secrete antibodies that bind to macrophages that have phagocytized an antigen, and they are subsequently destroyed by T-killer cells (T-kill). Mast cells (Mast) release histamine as a response to binding of an antigen to IgE molecules present in their cell membranes. The black crosses indicate position where sponge-derived immunosuppressive compounds interfere with the immune response.</p>
</caption>
<graphic xlink:href="10126_2004_405_f5" id="MO12"></graphic>
</fig>
</p>
<p>Three polyoxygenated sterols from a
<italic>Dysidea</italic>
sp. from Northern Australia are selective immunosuppressive compounds that inhibit the binding of interleukin 8 (IL-8), a cytokine that attracts neutrophils into an area of tissue injury, to the IL-8 receptor (
<xref ref-type="bibr" rid="CR107">Leone et al., 2000</xref>
). The simplexides from the Caribbean sponge
<italic>Plakortis simplex</italic>
are a group of immunosuppressive glycolipids that inhibit proliferation of activated T cells by a noncytotoxic mechanism (
<xref ref-type="bibr" rid="CR35">Costantino et al., 1999</xref>
). Pateamine A, from a
<italic>Mycale</italic>
sp., inhibits the production of IL-2 (
<xref ref-type="bibr" rid="CR156">Romo et al., 1998</xref>
) and thereby the activation of resting T cells and B cells to a lesser extent. Contignasterol from
<italic>Petrosia contignata</italic>
(
<xref ref-type="bibr" rid="CR25">Burgoyne and Andersen, 1992</xref>
) inhibits allergen-induced histamine release from rat mast cells (
<xref ref-type="bibr" rid="CR179">Takei et al., 1994</xref>
) and from guinea-pig lung tissue in vitro (
<xref ref-type="bibr" rid="CR23">Bramley et al., 1995</xref>
), and the activation of eosinophils into airways in guinea-pigs and could be used to treat asthma (
<xref ref-type="bibr" rid="CR105">Langlands et al., 1995</xref>
).</p>
</sec>
<sec id="Sec6">
<title>Cardiovascular Agents</title>
<p>In addition to regulators of the white blood cells, a number of sponge-derived molecules have been found to interfere with other blood-related diseases such as thrombosis, atherosclerosis, or diabetes (Table 
<xref rid="Tab4" ref-type="table">4</xref>
). The process of blood coagulation is triggered by a complex proteolytic cascade that leads to the formation of fibrin. Thrombin is a serine protease that cleaves a peptide fragment from fibrinogen, which then leads to the generation of fibrin, a major component of blood clots (
<xref ref-type="bibr" rid="CR170">Shuman et al., 1993</xref>
). Cyclotheonarnide A, isolated from a
<italic>Theonella</italic>
sp. (
<xref ref-type="bibr" rid="CR63">Fusetani et al., 1990</xref>
), represents an unusual class of serine protease inhibitors and is a potential drug for the treatment of thrombosis (
<xref ref-type="bibr" rid="CR115">Maryanoff et al., 1993</xref>
). Eryloside F from
<italic>Erylus formosus</italic>
was found to be a potent thrombin receptor antagonist (
<xref ref-type="bibr" rid="CR174">Stead et al., 2000</xref>
). Thrombin receptor activation is likely to play a key role not only in arterial thrombosis but also in atherosclerosis (
<xref ref-type="bibr" rid="CR32">Chackalamannil, 2001</xref>
). Atherosclerosis starts with damage to the endothelium and subsequent deposition of fats, cholesterol platelets, cellular waste products, calcium, and other substances in the artery wall. These may stimulate endothelial cells to produce a vascular cell adhesion molecule that results in further buildup of cells and shrinkage of the arterial diameter (
<xref ref-type="bibr" rid="CR197">Zapolska-Downar et al., 2001</xref>
). Halichlorine from
<italic>Halichondria okadai</italic>
is an inhibitor of the expression of vascular cell adhesion molecule 1 (
<xref ref-type="bibr" rid="CR102">Kuramoto et al., 1996</xref>
) and may thus impede atherogenesis (
<xref ref-type="bibr" rid="CR7">Arimoto et al., 1998</xref>
).
<table-wrap id="Tab4">
<label>Table 4</label>
<caption>
<p>Examples of Sponge Products that Affect Blood-Related Diseases</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Mode of Action</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Cyclotheonamide A</td>
<td align="left">Cyclic pentapeptide</td>
<td align="left">
<italic>Theonella</italic>
sp./Lithistida</td>
<td align="left">Serine protease inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR115">Maryanoff et al., 1993</xref>
</td>
</tr>
<tr>
<td align="left">Eryloside F</td>
<td align="left">Penasterol disaccharide</td>
<td align="left">
<italic>Eryltus formosus</italic>
/Astrophorida</td>
<td align="left">Thrombin receptor antagonist</td>
<td align="left">
<xref ref-type="bibr" rid="CR174">Stead et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Halichlorine</td>
<td align="left">Cyclic aza-polyketide</td>
<td align="left">
<italic>Halichondria okadai</italic>
/Halichondrida</td>
<td align="left">VCAM-1 inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR7">Arimoto et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Callyspongynic acid</td>
<td align="left">Polyacetylene</td>
<td align="left">
<italic>Callyspongia truncata</italic>
/Haplosclerida</td>
<td align="left">α-glucosidase inhibitor
<sup>a</sup>
</td>
<td align="left">
<xref ref-type="bibr" rid="CR131">Nakao et al., 2002</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>
<sup>a</sup>
Also has potential antiviral activity.</p>
</table-wrap-foot>
</table-wrap>
</p>
<p>Callyspongynic acid, isolated from
<italic>Callyspongia truncata</italic>
, is an α-glucosidase inhibitor (
<xref ref-type="bibr" rid="CR131">Nakao et al., 2002</xref>
). α-Glucosidase inhibitors interfere with the hydrolysis of glycogen, keeping the glucose concentration in the blood at a lower level, and can be used to treat patients with diabetes (
<xref ref-type="bibr" rid="CR106">Lebovitz, 1992</xref>
).</p>
</sec>
<sec id="Sec7">
<title>Neurosuppressive Compounds</title>
<p>Keramidine, isolated from an
<italic>Agelas</italic>
sp. (
<xref ref-type="bibr" rid="CR130">Nakamura et al., 1984</xref>
), is an example of a number of neurosuppressive compounds that have been isolated from marine sponges (Table 
<xref rid="Tab5" ref-type="table">5</xref>
). It is a serotonergic receptor antagonist and blocks serotonin-mediated neural communication. Several different serotonin receptors have been identified. They are related to (1) platelet aggregation, and may therefore be useful against thrombosis (
<xref ref-type="bibr" rid="CR158">Ruomei et al., 1996</xref>
); (2) smooth muscle contraction (
<xref ref-type="bibr" rid="CR66">Garcia-Colunga and Miledi, 1996</xref>
); (3) vomiting, owing to their presence in the gastrointestinal tract (
<xref ref-type="bibr" rid="CR104">Lang and Marvig, 1989</xref>
); (4) and most interestingly, may function as antidepressant drugs in the brain (
<xref ref-type="bibr" rid="CR128">Nagayama et al., 1980</xref>
).
<table-wrap id="Tab5">
<label>Table 5</label>
<caption>
<p>Examples of Neurosuppressives and Muscle Relaxants from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Mode of action</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Dysiherbaine</td>
<td align="left">Unusual amino acid</td>
<td align="left">
<italic>Dysidea herbacea</italic>
/Dendroceratida</td>
<td align="left">Glutamate receptor antagonist</td>
<td align="left">
<xref ref-type="bibr" rid="CR161">Sakai et al., 1997</xref>
</td>
</tr>
<tr>
<td align="left">Keramadine</td>
<td align="left">Pyrrole-guanidine alkaloid</td>
<td align="left">
<italic>Agelas</italic>
sp. / Agelasida</td>
<td align="left">Serotonergic receptor antagonist</td>
<td align="left">
<xref ref-type="bibr" rid="CR130">Nakamura et al., 1984</xref>
</td>
</tr>
<tr>
<td align="left">1-Methylisoguanosine</td>
<td align="left">Nucleoside analogue</td>
<td align="left">
<italic>Tedania digitata</italic>
/Poecilosclerida</td>
<td align="left">Unknown (muscle relaxant, antiallergic)</td>
<td align="left">
<xref ref-type="bibr" rid="CR148">Quinn et al., 1980</xref>
</td>
</tr>
<tr>
<td align="left">Xestospongin C</td>
<td align="left">Macrocyclic bis-oxaquinolizidine</td>
<td align="left">
<italic>Xestospongia</italic>
sp./Haplosclerida</td>
<td align="left">IP
<sub>3</sub>
-inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR47">De Smet et al.,1999</xref>
</td>
</tr>
<tr>
<td align="left">Okinonellin B</td>
<td align="left">Furanosesterterpenoid</td>
<td align="left">
<italic>Spongionella</italic>
sp./Dendroceratida</td>
<td align="left">Unknown (muscle relaxant)</td>
<td align="left">
<xref ref-type="bibr" rid="CR89">Kato et al., 1986</xref>
</td>
</tr>
<tr>
<td align="left">Bromotopsentin</td>
<td align="left">Bis-indole alkaloid</td>
<td align="left">
<italic>Spongosorites</italic>
sp./Halichondrida</td>
<td align="left">α
<sub>1</sub>
-Adrenergic receptor antagonist</td>
<td align="left">
<xref ref-type="bibr" rid="CR143">Phife et al., 1996</xref>
</td>
</tr>
<tr>
<td align="left">Penaresidin A</td>
<td align="left">Azetidine alkaloid</td>
<td align="left">
<italic>Penares</italic>
sp./Astrophorida</td>
<td align="left">Actomyosin ATPase inhibitor</td>
<td align="left">
<xref ref-type="bibr" rid="CR93">Kobayashi et al., 1991</xref>
</td>
</tr>
<tr>
<td align="left">S1319</td>
<td align="left">Benzothiazole derivative</td>
<td align="left">
<italic>Dysidea</italic>
sp./Dendroceratida</td>
<td align="left">Unknown (antiasthmatic, uterine relaxation)</td>
<td align="left">
<xref ref-type="bibr" rid="CR178">Suzuki et al., 1999</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
<p>Dysiherbaine from
<italic>Dysidea herbacea</italic>
(
<xref ref-type="bibr" rid="CR161">Sakai et al., 1997</xref>
) is a potent excitatory amino acid that causes seizures by interfering with the
<sc>L</sc>
-glutamate-based neurotransmitter communication and may provide a lead compound in therapeutical agents for neurologic disorders (
<xref ref-type="bibr" rid="CR162">Sakai et al., 2001</xref>
).</p>
</sec>
<sec id="Sec8">
<title>Muscle Relaxants</title>
<p>Disturbances in neuromuscular communication resulting from stress cause permanent muscle activation (
<xref ref-type="bibr" rid="CR112">Lundberg, 1995</xref>
;
<xref ref-type="bibr" rid="CR50">Edgar et al., 2002</xref>
). In addition to the above-mentioned centrally acting muscle relaxants, which mediate neuromuscular communication, peripherally acting muscle relaxant may be used for local muscle relaxation. They are applied for relief of strokes, or during intubations and surgery (
<xref ref-type="bibr" rid="CR59">Frakes, 2001</xref>
). 1-Methylguanosine from
<italic>Tedania digitata</italic>
(
<xref ref-type="bibr" rid="CR148">Quinn et al., 1980</xref>
) and xestospongin C, which was isolated from a
<italic>Xestospongia</italic>
sp. (
<xref ref-type="bibr" rid="CR65">Gafni et al., 1997</xref>
), are examples of muscle relaxants that discovered in sponges (Table 
<xref rid="Tab5" ref-type="table">5</xref>
). Xestospongin C is a potent inhibitor of the inositol 1,4,5-triphosphate (IP
<sub>3</sub>
) receptors and the endoplasmic-reticulum Ca
<sup>2+</sup>
pumps (
<xref ref-type="bibr" rid="CR47">De Smet et al., 1999</xref>
) and inhibits IP
<sub>3</sub>
-induced increase in the oscillatory contraction of muscles (
<xref ref-type="bibr" rid="CR120">Miyamoto et al., 2000</xref>
). ß-Adrenoreceptor agonists, such as S1319 isolated from a
<italic>Dysidea</italic>
sp. (
<xref ref-type="bibr" rid="CR178">Suzuki et al., 1999</xref>
), have utero-relaxant properties, which can be therapeutically used for the preterm delivery of infants (
<xref ref-type="bibr" rid="CR44">Dennedy et al., 2002</xref>
), and are widely used as antiasthmatic drugs (
<xref ref-type="bibr" rid="CR178">Suzuki et al., 1999</xref>
). However, owing to their low selectivity ß-adrenoreceptor agonists may have severe side effects such as arterial hypertension, corony heart disease, and tachycardia (
<xref ref-type="bibr" rid="CR20">Borchard, 1998</xref>
). Therefore, there is continued interest in finding more selective ß-adrenoreceptor agonists such as S1319.</p>
</sec>
<sec id="Sec9">
<title>Antiviral Compounds</title>
<p>Sponges are also a rich source of compounds with antiviral properties (Table 
<xref rid="Tab6" ref-type="table">6</xref>
). The high number of HIV-inhibiting compounds discovered does not reflect greater potential of sponges to fight AIDS compared with other viral diseases, but rather the interest of many researchers. The strong focus on screening for anti-HIV activity has led to discovery of numerous compounds, but the mechanism of inhibition is still poorly characterized. Papuamides C and D (
<xref ref-type="bibr" rid="CR58">Ford et al., 1999</xref>
), haplosamates A and B (
<xref ref-type="bibr" rid="CR149">Qureshi and Faulkner, 1999</xref>
), and avarol (
<xref ref-type="bibr" rid="CR126">Muller et al., 1987</xref>
), which has also been patented as antipsoriasis (
<xref ref-type="bibr" rid="CR127">Muller et al., 1991</xref>
), are examples of HIV-inhibiting compounds from different sponges. Avarol is one of the few compounds for which the mechanism by which it inhibits progression of HIV infection is more or less known. In vitro and animal data indicate that avarol combines useful properties of an increased humoral immune response, as IgG and IgM production is significantly increased, and interference with the posttranscriptional processes of viral infection (
<xref ref-type="bibr" rid="CR126">Muller et al., 1987</xref>
). Avarol inhibits HIV by almost completely blocking the synthesis of the natural UAG suppressor glutamine transfer tRNA. Synthesis of this tRNA is upregulated after viral infection, and it is important for the synthesis of a viral protease, which is necessary for viral proliferation (
<xref ref-type="bibr" rid="CR123">Muller and Schroder, 1991</xref>
). Low concentrations of only 0.9 and 0.3 μM avarol resulted in 80% and 50% inhibition of virus release from infected cells, respectively (
<xref ref-type="bibr" rid="CR165">Schroder et al., 1991</xref>
), while uninfected cells were highly resistant against avarol (
<xref ref-type="bibr" rid="CR125">Muller et al., 1985</xref>
;
<xref ref-type="bibr" rid="CR101">Kuchino et al., 1988</xref>
). Furthermore, it was shown that the avarol derivatives, 6′-hydroxy avarol and 3′-hydroxy avarone (Figure 
<xref rid="Fig6" ref-type="fig">6</xref>
), were very potent inhibitors of HIV reverse transcriptase. This enzyme has a key role in the early stages of HIV infection and is a specific target for antiviral drugs, as it is responsible for converting the viral genomic RNA into proviral double-stranded DNA, which is subsequently integrated into the host chromosomal DNA (
<xref ref-type="bibr" rid="CR111">Loya and Hizi, 1990</xref>
).
<table-wrap id="Tab6">
<label>Table 6</label>
<caption>
<p>Examples of Antiviral Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Activity</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Dragmacidin F</td>
<td align="left">Indole alkaloid</td>
<td align="left">
<italic>Halicortex</italic>
sp./?</td>
<td align="left">Antiviral</td>
<td align="left">
<xref ref-type="bibr" rid="CR37">Cutignano et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Papuamides C and D</td>
<td align="left">Cyclic peptide</td>
<td align="left">
<italic>Theonella mirabilis, T. swinhoei</italic>
/Lithistida</td>
<td align="left">Antiviral (HIV-1)</td>
<td align="left">
<xref ref-type="bibr" rid="CR58">Ford et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Mololipids</td>
<td align="left">Tyramine lipid</td>
<td align="left">?/Verongida</td>
<td align="left">Antiviral (HIV-1)</td>
<td align="left">
<xref ref-type="bibr" rid="CR157">Ross et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Haplosamates A and B</td>
<td align="left">Sulfamated steroid</td>
<td align="left">
<italic>Xestospongia</italic>
sp./Haplosclerida</td>
<td align="left">Antiviral (HIV-1 integrase inhibitor)</td>
<td align="left">
<xref ref-type="bibr" rid="CR149">Qureshi and Faulkner, 1999</xref>
</td>
</tr>
<tr>
<td align="left">Hamigeran B</td>
<td align="left">Phenolic macrolide</td>
<td align="left">
<italic>Hamigera tarangaensis</italic>
/Poecilosclerida</td>
<td align="left">Antiviral (herpes and polio)</td>
<td align="left">
<xref ref-type="bibr" rid="CR191">Wellington et al., 2000</xref>
</td>
</tr>
<tr>
<td align="left">Weinbersterols A and B</td>
<td align="left">Sulfated sterol</td>
<td align="left">
<italic>Petrosia weinbergi</italic>
/Haplosclerida</td>
<td align="left">Antiviral (feline leukemia, mouse influenza, mouse corona)</td>
<td align="left">
<xref ref-type="bibr" rid="CR177">Sun et al., 1991</xref>
</td>
</tr>
<tr>
<td align="left">Variolin B</td>
<td align="left">Pyridopyrrolopyrimidine alkaloid</td>
<td align="left">
<italic>Kirkpatrickia varialosa</italic>
/Poecilosclerida</td>
<td align="left">Antiviral</td>
<td align="left">
<xref ref-type="bibr" rid="CR141">Perry et al., 1994</xref>
</td>
</tr>
<tr>
<td align="left">Avarol</td>
<td align="left">Hydroquinone, sesquiterpenoid</td>
<td align="left">
<italic>Dysidea avara</italic>
/Dendroceratida</td>
<td align="left">UAG suppressor glutamine tRNA inhibitor
<sup>a</sup>
</td>
<td align="left">
<xref ref-type="bibr" rid="CR126">Muller et al., 1987</xref>
;
<xref ref-type="bibr" rid="CR127">Muller et al., 1991</xref>
</td>
</tr>
<tr>
<td align="left">2-5A</td>
<td align="left">2′, 5′ Linked oligonucleotide</td>
<td align="left">Many sponges</td>
<td align="left">Interferon mediator</td>
<td align="left">
<xref ref-type="bibr" rid="CR91">Kelve et al., 2003</xref>
</td>
</tr>
<tr>
<td align="left">Hennoxazole A</td>
<td align="left">Bisoxazole</td>
<td align="left">
<italic>Polyfibrospongia</italic>
sp./Dictyoceratida</td>
<td align="left">Antiviral</td>
<td align="left">
<xref ref-type="bibr" rid="CR81">Ichiba et al., 1991</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>
<sup>a</sup>
Also has antiinflammatory potential antitumor activity.</p>
</table-wrap-foot>
</table-wrap>
<fig id="Fig6">
<label>Figure 6</label>
<caption>
<p>Molecular structures of avarol (
<bold>a:</bold>
R1 = H) and 6′-hydroxy avarol (
<bold>a:</bold>
R1 = OH) and avarone (
<bold>b:</bold>
R1 = H) and 3′-hydroxy avarone (
<bold>b:</bold>
R1 = OH).</p>
</caption>
<graphic xlink:href="10126_2004_405_f6" id="MO13"></graphic>
</fig>
</p>
<p>In addition to their applications to treat diabetes, α-glucosidase inhibitors, such as callyspongymc acid, are potentially broad-based antiviral agents. They disturb protein glycosylation and cause some viral envelope proteins to be misfolded, which leads to arrest of these proteins within the endoplasmic reticulum, where protein folding takes place. It has been demonstrated that alteration of the glycosylation pattern of HIV, hepatitis B virus, and bovine viral diarrhea virus by α-glucosidase inhibitors attenuates viral infectivity (
<xref ref-type="bibr" rid="CR154">Ratner et al., 1991</xref>
;
<xref ref-type="bibr" rid="CR118">Mehta et al., 1998</xref>
).</p>
<p>A very different class of virus inhibitors that has been found in many different sponges are 2′-5′ oligoadenylates (2–5A), which are involved in the interferon-mediated response against a wide range of viruses in mammals. The antiviral action is based on the activation of a latent endoribonuclease that prevents viral replication by degradation of its mRNA as well as cellular RNA (
<xref ref-type="bibr" rid="CR91">Kelve et al., 2003</xref>
). For many other antivirals, the mechanism of inhibition is still unclear, but they are active against range of viruses. Hamigeran B from
<italic>Hamigera tarangaensis</italic>
, for example, showed 100 % in vitro inhibition against both the herpes and polio viruses (
<xref ref-type="bibr" rid="CR191">Wellington et al., 2000</xref>
), and the weinbersterols A and B from
<italic>Petrosia weinbergi</italic>
exhibited in vitro activity against feline leukemia virus, mouse influenza virus, and mouse corona virus (
<xref ref-type="bibr" rid="CR177">Sun et al., 1991</xref>
;
<xref ref-type="bibr" rid="CR96">Koehn et al., 1991</xref>
).</p>
<p>In general, antiviral molecules from sponges do not give protection against viruses, but they may result in drugs to treat already infected persons. In addition, broad-based antiviral agents such as 2-5A and α-glucosidase inhibitors may be useful in cases of sudden outbreaks of (unfamiliar) viruses like SARS and Ebola.</p>
</sec>
<sec id="Sec10">
<title>Antimalarial Compounds</title>
<p>Several sponge-derived antimalarial compounds have been discovered during the last decade (Table 
<xref rid="Tab7" ref-type="table">7</xref>
). New antimalarial drugs are needed to cope with the increasing number of multidrug-resistant
<italic>Plasmodium</italic>
strains that cause malaria.
<italic>Plasmodium falciparum</italic>
has become resistant against chloroquinone, pyrimethamine, and sulfadoxine (
<xref ref-type="bibr" rid="CR28">Bwijo et al., 2003</xref>
). Kalihinol A from a
<italic>Acanthella</italic>
sp. (
<xref ref-type="bibr" rid="CR121">Miyaoka et al., 1998</xref>
) and a number of terpenoid isocyanates, isothiocyanates, and isonitriles from
<italic>Cymbastela hooperi</italic>
(
<xref ref-type="bibr" rid="CR98">Konig et al., 1996</xref>
) display selective in vitro antimalarial activity against
<italic>P. falciparum</italic>
. Also a number of free carboxylic acids from
<italic>Diacarnus levii</italic>
were used as precursors to yield new cyclic norditerpene peroxides after esterification. These epidioxy-substituted norditerpenes and norsesterterpenes displayed selective activity against both chloroquine-sensitive and chloroquine-resistant
<italic>P. falciparum</italic>
strains (
<xref ref-type="bibr" rid="CR39">D’ Ambrosio et al., 1998</xref>
). The manzamines, the most promising antimalarial compound, have been discovered in a number of sponges (
<xref ref-type="bibr" rid="CR160">Sakai et al., 1986</xref>
;
<xref ref-type="bibr" rid="CR3">Ang et al., 2000</xref>
;
<xref ref-type="bibr" rid="CR196">Youssaf et al., 2002</xref>
). It has been suggested that the antimalarial effect of manzamine A is due to an enhanced immune response (
<xref ref-type="bibr" rid="CR4">Ang et al., 2001</xref>
).
<table-wrap id="Tab7">
<label>Table 7</label>
<caption>
<p>Examples of Antimalarial Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Axisonitrile-3</td>
<td align="left">Sesquiterpenoid isocyanide</td>
<td align="left">
<italic>Acanthella klethra</italic>
/Halichondrida</td>
<td align="left">
<xref ref-type="bibr" rid="CR5">Angerhofer et al., 1992</xref>
</td>
</tr>
<tr>
<td align="left">Manzamine A</td>
<td align="left">Manzamine alkaloid, diterpene isocyanates, isothiocyanates and isonitriles, norditerpenoid and norsesterterpenoid endoperoxides</td>
<td align="left">e.g., Haliclona sp./Haplosclerida</td>
<td align="left">
<xref ref-type="bibr" rid="CR4">Ang et al., 2001</xref>
</td>
</tr>
<tr>
<td align="left"></td>
<td align="left"></td>
<td align="left">
<italic>Cymbastela</italic>
hooperi/Halichondrida</td>
<td align="left">
<xref ref-type="bibr" rid="CR98">Konig et al., 1996</xref>
</td>
</tr>
<tr>
<td align="left"></td>
<td align="left"></td>
<td align="left">
<italic>Diacarnus levii</italic>
/Poecilosclerida</td>
<td align="left">
<xref ref-type="bibr" rid="CR39">D’Ambrosio et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Kalihinol A</td>
<td align="left">Isonitril-containing kalihinane diterpenoid</td>
<td align="left">
<italic>Acanthella </italic>
sp./Halichondrida1</td>
<td align="left">
<xref ref-type="bibr" rid="CR121">Miyaoka et al., 1998</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
</sec>
<sec id="Sec11">
<title>Antibiotics and Fungicides</title>
<p>With respect to antibiotics and fungicides, similar multiresistance problems have concerned physicians for a long time. Many new molecules with antibiotic properties are discovered every year, but in marine sponges their ubiquity is remarkable (Table 
<xref rid="Tab8" ref-type="table">8</xref>
). An early screening by
<xref ref-type="bibr" rid="CR26">Burkholder and Ruetzler (1969)</xref>
revealed that 18 of 31 sponges tested showed antimicrobial effects, of which some were very strong against a range of gram-positive and gram-negative bacteria. The added value of some new sponge-derived antibiotics was shown by the inhibitory effect of arenosclerins A–C from
<italic>Arenosclera brasiliensis</italic>
on 12 antibiotic-resistant bacteria isolated from a hospital (
<xref ref-type="bibr" rid="CR183">Torres et al., 2002</xref>
). Fungicides that are currently used are less diverse than antimicrobials, and the use of many of them is restricted because of toxic effects to humans, animals, and plants (
<xref ref-type="bibr" rid="CR129">Nakagawa and Moore, 1995</xref>
;
<xref ref-type="bibr" rid="CR150">Rahden-Staron, 2002</xref>
). It remains to be demonstrated whether antifungals like topsentiasterols D and E from
<italic>Topsentia</italic>
sp. (
<xref ref-type="bibr" rid="CR64">Fusetani et al., 1994</xref>
), acanthosterol sulfates I and J from an
<italic>Acanthodendrilla</italic>
sp. (
<xref ref-type="bibr" rid="CR186">Tsukamoto et al., 1998</xref>
) or the macrolide leucascandrolide A from the calcareous sponge
<italic>Leucascandra caveolata</italic>
(
<xref ref-type="bibr" rid="CR38">D’Ambrosio et al., 1996</xref>
) will have different characteristics than the fungicides that are currently used, but the fact that they are produced by eukaryotic organism (if not produced by a symbiont) may imply that they are less toxic to other nonfungal eukaryotes.
<table-wrap id="Tab8">
<label>Table 8</label>
<caption>
<p>Examples of Antibacterial and Antifungal Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Activity</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Discodermins B, C, and D</td>
<td align="left">Cyclic peptide</td>
<td align="left">
<italic>Discodermia kiiensis</italic>
/Lithistida</td>
<td align="left">Antibacterial</td>
<td align="left">
<xref ref-type="bibr" rid="CR116">Matsunaga et al., 1985</xref>
</td>
</tr>
<tr>
<td align="left">Topsentiasterol sulfates A–E</td>
<td align="left">Sulfated sterol</td>
<td align="left">
<italic>Topsentia</italic>
sp./Halichondrida</td>
<td align="left">Antibacterial/antifungal (D and E)</td>
<td align="left">
<xref ref-type="bibr" rid="CR64">Fusetani et al., 1994</xref>
</td>
</tr>
<tr>
<td align="left">Arenosclerins A, B, and C</td>
<td align="left">Alkylpiperidine alkaloid</td>
<td align="left">
<italic>Arenosclera brasiliensis</italic>
/Haplosclerida</td>
<td align="left">Antibacterial</td>
<td align="left">
<xref ref-type="bibr" rid="CR183">Torres et al., 2002</xref>
</td>
</tr>
<tr>
<td align="left">Axinellamines B–D</td>
<td align="left">Imidazo-azolo-imidazole alkaloid</td>
<td align="left">
<italic>Axinella</italic>
sp./Halichondrida</td>
<td align="left">Antibacterial</td>
<td align="left">
<xref ref-type="bibr" rid="CR189">Urban et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Acanthosterol I and J</td>
<td align="left">Sulfated sterol</td>
<td align="left">
<italic>Acanthodendrilla</italic>
sp./Dendroceratida</td>
<td align="left">Antifungal</td>
<td align="left">
<xref ref-type="bibr" rid="CR186">Tsukamoto et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Oceanapiside</td>
<td align="left">Bisaminohydroxylipid glycoside</td>
<td align="left">
<italic>Oceanapia phillipensis</italic>
/Haplosclerida</td>
<td align="left">Antifungal</td>
<td align="left">
<xref ref-type="bibr" rid="CR132">Nicolas et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Spongistatin</td>
<td align="left">Polyether macrolide lactone</td>
<td align="left">
<italic>Hyrtios erecta</italic>
/Dictyoceratida</td>
<td align="left">Antifungal</td>
<td align="left">
<xref ref-type="bibr" rid="CR142">Pettit et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Leucascandrolide A</td>
<td align="left">Oxazole-containing polyether macrolide</td>
<td align="left">
<italic>Leucascandra caveolata</italic>
/Calcarea</td>
<td align="left">Antifungal</td>
<td align="left">
<xref ref-type="bibr" rid="CR38">D’Ambrosio et al., 1996</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
</sec>
<sec id="Sec12">
<title>Antifouling Compounds</title>
<p>A last class of bioactive compounds from marine sponges are antifouling molecules (Table 
<xref rid="Tab9" ref-type="table">9</xref>
). They are not associated with the development of new drugs, but could be environmentally friendly substitutes for chemical antifoulants. Biofouling organisms such as blue mussels, barnacles, and macroalgae cause serious problems to ship’s hulls, cooling systems of power plants, and aquaculture materials (
<xref ref-type="bibr" rid="CR78">Holmes, 1970</xref>
;
<xref ref-type="bibr" rid="CR80">Houghton, 1978</xref>
). Long-term use of chemical antifoulants has led to increased concentrations of tributyltin and its current replacements in coastal sediments (
<xref ref-type="bibr" rid="CR99">Konstantinou and Albanis, 2004</xref>
) and to mortality and change of sex of nontarget organisms (
<xref ref-type="bibr" rid="CR90">Katranitsas et al., 2003</xref>
). Natural marine antifouling molecules have recently been reviewed (
<xref ref-type="bibr" rid="CR61">Fusetani, 2004</xref>
) and may provide less toxic and more specific antifouling activity. Sponge-derived antifouling molecules have been found to inhibit the settlement of barnacle larvae (
<xref ref-type="bibr" rid="CR137">Okino et al., 1995</xref>
;
<xref ref-type="bibr" rid="CR184">Tsukamoto et al., 1996a</xref>
,
<xref ref-type="bibr" rid="CR185">1996b)</xref>
, inhibit fouling by macroalgae (
<xref ref-type="bibr" rid="CR72">Hattori et al., 1998</xref>
;
<xref ref-type="bibr" rid="CR100">Kubanek et al., 2002</xref>
), or repell the blue mussel
<italic>Mytilus edulis galloprovincialis</italic>
(
<xref ref-type="bibr" rid="CR167">Sera et al., 1999</xref>
).
<table-wrap id="Tab9">
<label>Table 9</label>
<caption>
<p>Examples of Antifouling Products from Sponges</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Compound</th>
<th align="left">Compound class</th>
<th align="left">Species/order</th>
<th align="left">Reference</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Kalihinene X</td>
<td align="left">Isocyanoterpenoid</td>
<td align="left">
<italic>Acanthella cavernosa</italic>
/Halichondrida</td>
<td align="left">
<xref ref-type="bibr" rid="CR137">Okino et al., 1995</xref>
</td>
</tr>
<tr>
<td align="left">Kalihipyran B</td>
<td align="left">Isocyanoterpenoid</td>
<td align="left">
<italic>Acanthella cavernosa</italic>
/Halichondrida</td>
<td align="left">
<xref ref-type="bibr" rid="CR138">Okino et al., 1996</xref>
</td>
</tr>
<tr>
<td align="left">10β-Formarnidokalihinol</td>
<td align="left">Isocyanoterpenoid</td>
<td align="left">
<italic>Acanthella cavernosa</italic>
/Halichondrida</td>
<td align="left">
<xref ref-type="bibr" rid="CR74">Hirota et al., 1996</xref>
</td>
</tr>
<tr>
<td align="left">Pseudoceratidine 2</td>
<td align="left">Dibromopyrrole-containing spermidine derivative</td>
<td align="left">
<italic>Pseudoceratina purpurea</italic>
/Verongida</td>
<td align="left">
<xref ref-type="bibr" rid="CR185">Tsukamoto et al., 1996b</xref>
</td>
</tr>
<tr>
<td align="left">Ceratinamide A and B</td>
<td align="left">Bromotyrosine derivative</td>
<td align="left">
<italic>Pseudoceratina purpurea</italic>
/Verongida</td>
<td align="left">
<xref ref-type="bibr" rid="CR184">Tsukamoto et al., 1996a</xref>
</td>
</tr>
<tr>
<td align="left">C
<sub>22</sub>
ceramide</td>
<td align="left">Ceramide</td>
<td align="left">
<italic>Haliclona koremella</italic>
/Haplosclerida</td>
<td align="left">
<xref ref-type="bibr" rid="CR72">Hattori et al., 1998</xref>
</td>
</tr>
<tr>
<td align="left">Formoside</td>
<td align="left">Striterpene glycoside, sterol diperoxide</td>
<td align="left">
<italic>Erylus formosus</italic>
/Astrophorida</td>
<td align="left">
<xref ref-type="bibr" rid="CR100">Kubanek et al., 2002</xref>
</td>
</tr>
<tr>
<td align="left"></td>
<td align="left"></td>
<td align="left">
<italic>Lendenfeldia chondrodes </italic>
/Dictyoceratida</td>
<td align="left">
<xref ref-type="bibr" rid="CR167">Sera et al., 1999</xref>
</td>
</tr>
<tr>
<td align="left">Axinyssimides</td>
<td align="left">Sesquiterpene carbonimide dichlorides</td>
<td align="left">
<italic>Axinyssa</italic>
sp./Halichondrida</td>
<td align="left">
<xref ref-type="bibr" rid="CR75">Hirota et al., 1998</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
</sec>
<sec id="Sec13">
<title>Ecologic Role of Sponge Metabolites</title>
<p>Such an extensive collection of sponge-derived bioactive compounds raises the question of why sponges produce so many metabolites that can be useful to treat our human diseases. The huge number of different secondary metabolites discovered in marine sponges and the complexity of the compounds and their biosynthetic pathways (and corresponding kilobases of DNA for the programming of their synthesis) can be regarded as an indication of their importance for survival. An obvious example of the benefits of their secondary metabolites for the sponge itself, is the presence of antifouling products. To safeguard their water-pumping capacity, sponges cannot tolerate biofilm formation or settlement of barnacles or bryozoans on their surface (
<xref ref-type="bibr" rid="CR146">Proksch, 1994</xref>
), The level of cytotoxicity of some sponge products is high enough to even create a bare zone around the sponge (
<xref ref-type="bibr" rid="CR182">Thompson, 1985</xref>
) that is maintained by the emission of a mucus containing the toxins (
<xref ref-type="bibr" rid="CR176">Sullivan et al., 1981</xref>
). This allows the conquest of densely populated rocks or corals and competition with faster growing organisms, but it is striking that the sponge can selectively use its poisons without self-destruction.</p>
<p>Secondary metabolites can protect the organism against predation, which is especially important for physically unprotected sessile organisms like sponges (
<xref ref-type="bibr" rid="CR12">Becerro et al., 1997</xref>
). Relatively few animals, such as the hawksbill turtle and some highly evolved teleost fishes (
<xref ref-type="bibr" rid="CR119">Meylan, 1990</xref>
), are largely dependent on sponges for their diet. Also some nudibranches feed on sponges and even manage to use the sponge’s metabolites for their own chemical defence (
<xref ref-type="bibr" rid="CR139">Pawlik et al., 1988</xref>
). However, these spongivores represent only a tiny fraction of the animals inhabiting the seas. Secondary metabolites can also protect their producers against bacteria, fungi, or parasites (
<xref ref-type="bibr" rid="CR40">Davies, 1992</xref>
). In sponges the role of the chemical constituents is clouded by the complexity of the sponge-symbiont relationship (
<xref ref-type="bibr" rid="CR48">Dumdei et al., 1998</xref>
). Many different bacterial species permanently inhabit sponges and contribute considerably to the total sponge biomass (
<xref ref-type="bibr" rid="CR192">Wilkinson, 1978</xref>
). It has been suggested that the growth of “useful” microorganisms may be under control of the sponge host and serve as source of food or supply other metabolic products (
<xref ref-type="bibr" rid="CR124">Muller et al., 1981</xref>
). However, it has also been found that associated bacteria might be the actual producers of a number of compounds that have been isolated from sponges.
<italic>Oscillatoria spongelia</italic>
, a cyanobacterial symbiont that can constitute up to 40% of
<italic>Dysidea herbacea</italic>
, is the producer of antimicrobial polybrominated biphenyl ethers and might keep the sponge free of other bacteria (
<xref ref-type="bibr" rid="CR188">Unson, et al., 1994</xref>
).</p>
<p>For many products it is not yet known whether they are produced by the sponge or by a symbiont. It is clear, however, that sponges are responsible for the production of a rich arsenal of “chemical weapons.” Their early appearance in evolution has given them a lot of time for the development of an advanced chemical defense system. It is interesting to note that the synthesis of secondary metabolites is regulated depending on conditions that the sponge experiences. Specimens of
<italic>Crambe crambe</italic>
in well-illuminated regions grow faster than their counterparts exposed to darker conditions, but the specimens in the dark are better defended as they accumulate higher concentrations of cytotoxic metabolites (
<xref ref-type="bibr" rid="CR187">Turon et al., 1998</xref>
). Another example is the production of halichondrin B by
<italic>Lissodendoryx</italic>
sp., which varies seasonally, with depth, and with the condition of the sponge. Halichondrin B yields could be enhanced by an order of magnitude during serial cloning, suggesting a defensive response to damage (
<xref ref-type="bibr" rid="CR11">Battershill et al., 2002</xref>
). The ability to stimulate the production of secondary metabolites by sponges is an important consideration when one wants to harvest compounds from sponges for the production of potential new medicines.</p>
</sec>
</sec>
<sec id="Sec14" sec-type="discussion">
<title>C
<sc>ONCLUSION</sc>
</title>
<p>Marine sponges produce an enormous array of antitumor, antiviral, antiinflammatory, immunosuppressive, antibiotic, and other bioactive molecules that can affect the pathogenesis of many human diseases. The relationship between the chemical structures of the secondary metabolites from sponges and the diseases they affect is usually not obvious. Different components affect the targeted disease by different mechanisms (e.g., microtubule stabilization or interaction with DNA to combat tumors). Moreover, inhibitors of transcription may be effective against both cancer and viral diseases. To make things more complex, there are many relations between, for instance, inflammation, cancer, and viral infections via the immune system, which plays a key role in certain responses of the body to these diseases. Chronic inflammation of the lungs by cigarette smoke often leads to lung cancer (
<xref ref-type="bibr" rid="CR136">Ohwada et al., 1995</xref>
) and cervical and liver cancer can follow chronic inflammation caused by papilloma viruses (
<xref ref-type="bibr" rid="CR171">Smith-McCune et al., 1996</xref>
) and hepatitis B and C viruses, respectively (
<xref ref-type="bibr" rid="CR198">Zhu et al., 1997</xref>
). In addition, limited activity testing (e.g., only on cell growth inhibition and not on antiviral properties) yields an incomplete overview of the actual properties of the metabolites. Finally, for many bioactive molecules from sponges, the exact mode of action and their origin (sponge or symbiont) are still unclear. Most bioactive metabolites from sponges are inhibitors of certain enzymes, which often mediate or produce mediators of intracellular or intercellular messengers involved in the pathogenesis of a disease. As this is usually a cascade of reactions inside the cell or tissue, many enzymes in the cascade are targets for potential therapy. The different enzymes in the cascade can be structurally completely different proteins; therefore, it is not surprising that a wide range of metabolites can be used for the treatment of one disease. This applies in particular to a complex disease, such as cancer, which is affected by so many different factors. Furthermore, antiviral molecules also appear to encamps a wide array of chemical structures, such as peptides, lipids, alkaloids, sterols, oligonucleotides, and a phenolic macrolide. A similar diverse pattern is observed for antibacterial and immunosuppressive metabolites. Most compounds that display antiinflammatory activity are sesterterpenoids. Nevertheless, in these cases the activity of the sponge metabolites is concentrated on certain steps; for instance, most antiinflammatory compounds act against phospholipase A
<sub>2</sub>
.</p>
<p>The potency of sponge-derived medicines lies in the fact that each of these thousands of metabolites and their derivatives has its own specific dose-related inhibitory effect, efficacy, and potential (diminished) side effects that determine its suitability for medicinal use. In addition, the skeleton or active core of these molecules may be used as a vehicle to develop derivatives with their own specific efficacy and side effects. Therefore, the most important challenge in transforming bioactive molecules into medicines is now to screen the treasure-house of sponge metabolites and select those that display a specific mode of action with the desired characteristics against a disease. An important question for the future remains how to actually prepare the potential novel drugs on a large scale.</p>
</sec>
</body>
<back>
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