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Host-Microbiome Cross-talk in Oral Mucositis

Identifieur interne : 000782 ( Pmc/Corpus ); précédent : 000781; suivant : 000783

Host-Microbiome Cross-talk in Oral Mucositis

Auteurs : R. M. Vasconcelos ; N. Sanfilippo ; B. J. Paster ; A. R. Kerr ; Y. Li ; L. Ramalho ; E. L. Queiroz ; B. Smith ; S. T. Sonis ; P. M. Corby

Source :

RBID : PMC:4914867

Abstract

Oral mucositis (OM) is among the most common, painful, and debilitating toxicities of cancer regimen–related treatment, resulting in the formation of ulcers, which are susceptible to increased colonization of microorganisms. Novel discoveries in OM have focused on understanding the host-microbial interactions, because current pathways have shown that major virulence factors from microorganisms have the potential to contribute to the development of OM and may even prolong the existence of already established ulcerations, affecting tissue healing. Additional comprehensive and disciplined clinical investigation is needed to carefully characterize the relationship between the clinical trajectory of OM, the local levels of inflammatory changes (both clinical and molecular), and the ebb and flow of the oral microbiota. Answering such questions will increase our knowledge of the mechanisms engaged by the oral immune system in response to mucositis, facilitating their translation into novel therapeutic approaches. In doing so, directed clinical strategies can be developed that specifically target those times and tissues that are most susceptible to intervention.


Url:
DOI: 10.1177/0022034516641890
PubMed: 27053118
PubMed Central: 4914867

Links to Exploration step

PMC:4914867

Le document en format XML

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<div type="abstract" xml:lang="en">
<p>Oral mucositis (OM) is among the most common, painful, and debilitating toxicities of cancer regimen–related treatment, resulting in the formation of ulcers, which are susceptible to increased colonization of microorganisms. Novel discoveries in OM have focused on understanding the host-microbial interactions, because current pathways have shown that major virulence factors from microorganisms have the potential to contribute to the development of OM and may even prolong the existence of already established ulcerations, affecting tissue healing. Additional comprehensive and disciplined clinical investigation is needed to carefully characterize the relationship between the clinical trajectory of OM, the local levels of inflammatory changes (both clinical and molecular), and the ebb and flow of the oral microbiota. Answering such questions will increase our knowledge of the mechanisms engaged by the oral immune system in response to mucositis, facilitating their translation into novel therapeutic approaches. In doing so, directed clinical strategies can be developed that specifically target those times and tissues that are most susceptible to intervention.</p>
</div>
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<journal-id journal-id-type="iso-abbrev">J. Dent. Res</journal-id>
<journal-id journal-id-type="publisher-id">JDR</journal-id>
<journal-id journal-id-type="hwp">spjdr</journal-id>
<journal-title-group>
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</journal-title-group>
<issn pub-type="ppub">0022-0345</issn>
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</article-categories>
<title-group>
<article-title>Host-Microbiome Cross-talk in Oral Mucositis</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Vasconcelos</surname>
<given-names>R.M.</given-names>
</name>
<xref ref-type="aff" rid="aff1-0022034516641890">1</xref>
<xref ref-type="aff" rid="aff2-0022034516641890">2</xref>
<xref ref-type="aff" rid="aff3-0022034516641890">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sanfilippo</surname>
<given-names>N.</given-names>
</name>
<xref ref-type="aff" rid="aff1-0022034516641890">1</xref>
<xref ref-type="aff" rid="aff4-0022034516641890">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Paster</surname>
<given-names>B.J.</given-names>
</name>
<xref ref-type="aff" rid="aff5-0022034516641890">5</xref>
<xref ref-type="aff" rid="aff6-0022034516641890">6</xref>
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<contrib contrib-type="author">
<name>
<surname>Kerr</surname>
<given-names>A.R.</given-names>
</name>
<xref ref-type="aff" rid="aff2-0022034516641890">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Li</surname>
<given-names>Y.</given-names>
</name>
<xref ref-type="aff" rid="aff2-0022034516641890">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ramalho</surname>
<given-names>L.</given-names>
</name>
<xref ref-type="aff" rid="aff3-0022034516641890">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Queiroz</surname>
<given-names>E.L.</given-names>
</name>
<xref ref-type="aff" rid="aff2-0022034516641890">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Smith</surname>
<given-names>B.</given-names>
</name>
<xref ref-type="aff" rid="aff1-0022034516641890">1</xref>
<xref ref-type="aff" rid="aff4-0022034516641890">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sonis</surname>
<given-names>S.T.</given-names>
</name>
<xref ref-type="aff" rid="aff7-0022034516641890">7</xref>
<xref ref-type="aff" rid="aff8-0022034516641890">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Corby</surname>
<given-names>P.M.</given-names>
</name>
<xref ref-type="aff" rid="aff1-0022034516641890">1</xref>
<xref ref-type="aff" rid="aff2-0022034516641890">2</xref>
<xref ref-type="corresp" rid="corresp1-0022034516641890"></xref>
</contrib>
</contrib-group>
<aff id="aff1-0022034516641890">
<label>1</label>
School of Medicine, New York University, New York, NY, USA</aff>
<aff id="aff2-0022034516641890">
<label>2</label>
College of Dentistry, New York University, New York, NY, USA</aff>
<aff id="aff3-0022034516641890">
<label>3</label>
Faculdade de Odontologia, Universidade Federal da Bahia, Salvador, BA, Brazil</aff>
<aff id="aff4-0022034516641890">
<label>4</label>
New York University Perlmutter Cancer Center, New York, NY, USA</aff>
<aff id="aff5-0022034516641890">
<label>5</label>
The Forsyth Institute, Cambridge, MA, USA</aff>
<aff id="aff6-0022034516641890">
<label>6</label>
Department of Oral Medicine, Infection & Immunity, Harvard School of Dental Medicine, Boston, MA, USA</aff>
<aff id="aff7-0022034516641890">
<label>7</label>
Biomodels, LLC, Watertown, MA, USA</aff>
<aff id="aff8-0022034516641890">
<label>8</label>
Brigham and Women’s Hospital and Dana-Farber Cancer Institute, Boston, MA, USA</aff>
<author-notes>
<corresp id="corresp1-0022034516641890">P.M. Corby, School of Medicine, New York University, One Park Avenue, New York, NY 10010, USA. Email:
<email>Patricia.Corby@nyumc.org</email>
</corresp>
<corresp id="corresp2-0022034516641890">S.T. Sonis, Division of Oral Medicine and Dentistry, Brigham and Women’s Hospital, 75 Francis Street, Boston, MA 02115, USA. Email:
<email>ssonis@Biomodels.com</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>06</day>
<month>4</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="ppub">
<month>7</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>1</day>
<month>7</month>
<year>2017</year>
</pub-date>
<pmc-comment> PMC Release delay is 12 months and 0 days and was based on the . </pmc-comment>
<volume>95</volume>
<issue>7</issue>
<fpage>725</fpage>
<lpage>733</lpage>
<permissions>
<copyright-statement>© International & American Associations for Dental Research 2016</copyright-statement>
<copyright-year>2016</copyright-year>
<copyright-holder content-type="society">International & American Associations for Dental Research</copyright-holder>
</permissions>
<abstract>
<p>Oral mucositis (OM) is among the most common, painful, and debilitating toxicities of cancer regimen–related treatment, resulting in the formation of ulcers, which are susceptible to increased colonization of microorganisms. Novel discoveries in OM have focused on understanding the host-microbial interactions, because current pathways have shown that major virulence factors from microorganisms have the potential to contribute to the development of OM and may even prolong the existence of already established ulcerations, affecting tissue healing. Additional comprehensive and disciplined clinical investigation is needed to carefully characterize the relationship between the clinical trajectory of OM, the local levels of inflammatory changes (both clinical and molecular), and the ebb and flow of the oral microbiota. Answering such questions will increase our knowledge of the mechanisms engaged by the oral immune system in response to mucositis, facilitating their translation into novel therapeutic approaches. In doing so, directed clinical strategies can be developed that specifically target those times and tissues that are most susceptible to intervention.</p>
</abstract>
<kwd-group>
<kwd>cancer</kwd>
<kwd>oral microbiome</kwd>
<kwd>Toll-like receptor</kwd>
<kwd>pathogen-associated molecular pattern</kwd>
<kwd>damage-associated molecular pattern</kwd>
<kwd>cancer complications</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
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