Serveur d'exploration sur le lymphœdème

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Preleukemia: one name, many meanings

Identifieur interne : 000132 ( Pmc/Checkpoint ); précédent : 000131; suivant : 000133

Preleukemia: one name, many meanings

Auteurs : H P Koeffler [États-Unis, Singapour] ; G. Leong [Singapour]

Source :

RBID : PMC:5339433

Abstract

Definition of preleukemia has evolved. It was first used to describe the myelodysplastic syndrome (MDS) with a propensity to progress to acute myeloid leukemia (AML). Individuals with germline mutations of either RUNX1, CEBPA, or GATA2 can also be called as preleukemic because they have a markedly increased incidence of evolution into AML. Also, alkylating chemotherapy or radiation can cause MDS/preleukemia, which nearly always progress to AML. More recently, investigators noted that AML patients who achieved complete morphological remission after chemotherapy often have clonal hematopoiesis predominantly marked by either DNMT3A, TET2 or IDH1/2 mutations, which were also present at diagnosis of AML. This preleukemic clone represents involvement of an early hematopoietic stem cells, which is resistant to standard therapy. The same clonal hematopoietic mutations have been identified in older ‘normal' individuals who have a modest increased risk of developing frank AML. These individuals have occasionally been said, probably inappropriately, to have a preleukemia clone. Our evolving understanding of the term preleukemia has occurred by advancing technology including studies of X chromosome inactivation, cytogenetics and more recently deep nucleotide sequencing.


Url:
DOI: 10.1038/leu.2016.364
PubMed: 27899806
PubMed Central: 5339433


Affiliations:


Links toward previous steps (curation, corpus...)


Links to Exploration step

PMC:5339433

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Preleukemia: one name, many meanings</title>
<author>
<name sortKey="Koeffler, H P" sort="Koeffler, H P" uniqKey="Koeffler H" first="H P" last="Koeffler">H P Koeffler</name>
<affiliation wicri:level="1">
<nlm:aff id="aff1">
<institution>Department of Hematology and Oncology, Cedars-Sinai Medical Center</institution>
, Los Angeles, CA,
<country>USA</country>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff2">
<institution>Cancer Science Institute of Singapore, National University of Singapore</institution>
,
<country>Singapore</country>
</nlm:aff>
<country xml:lang="fr">Singapour</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff3">
<institution>National University Cancer Institute of Singapore, National University Hospital</institution>
,
<country>Singapore</country>
</nlm:aff>
<country xml:lang="fr">Singapour</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Leong, G" sort="Leong, G" uniqKey="Leong G" first="G" last="Leong">G. Leong</name>
<affiliation wicri:level="1">
<nlm:aff id="aff2">
<institution>Cancer Science Institute of Singapore, National University of Singapore</institution>
,
<country>Singapore</country>
</nlm:aff>
<country xml:lang="fr">Singapour</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PMC</idno>
<idno type="pmid">27899806</idno>
<idno type="pmc">5339433</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339433</idno>
<idno type="RBID">PMC:5339433</idno>
<idno type="doi">10.1038/leu.2016.364</idno>
<date when="2017">2017</date>
<idno type="wicri:Area/Pmc/Corpus">000987</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000987</idno>
<idno type="wicri:Area/Pmc/Curation">000987</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">000987</idno>
<idno type="wicri:Area/Pmc/Checkpoint">000132</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">000132</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a" type="main">Preleukemia: one name, many meanings</title>
<author>
<name sortKey="Koeffler, H P" sort="Koeffler, H P" uniqKey="Koeffler H" first="H P" last="Koeffler">H P Koeffler</name>
<affiliation wicri:level="1">
<nlm:aff id="aff1">
<institution>Department of Hematology and Oncology, Cedars-Sinai Medical Center</institution>
, Los Angeles, CA,
<country>USA</country>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff2">
<institution>Cancer Science Institute of Singapore, National University of Singapore</institution>
,
<country>Singapore</country>
</nlm:aff>
<country xml:lang="fr">Singapour</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff3">
<institution>National University Cancer Institute of Singapore, National University Hospital</institution>
,
<country>Singapore</country>
</nlm:aff>
<country xml:lang="fr">Singapour</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Leong, G" sort="Leong, G" uniqKey="Leong G" first="G" last="Leong">G. Leong</name>
<affiliation wicri:level="1">
<nlm:aff id="aff2">
<institution>Cancer Science Institute of Singapore, National University of Singapore</institution>
,
<country>Singapore</country>
</nlm:aff>
<country xml:lang="fr">Singapour</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Leukemia</title>
<idno type="ISSN">0887-6924</idno>
<idno type="eISSN">1476-5551</idno>
<imprint>
<date when="2017">2017</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Definition of preleukemia has evolved. It was first used to describe the myelodysplastic syndrome (MDS) with a propensity to progress to acute myeloid leukemia (AML). Individuals with germline mutations of either
<italic>RUNX1</italic>
,
<italic>CEBPA</italic>
, or
<italic>GATA2</italic>
can also be called as preleukemic because they have a markedly increased incidence of evolution into AML. Also, alkylating chemotherapy or radiation can cause MDS/preleukemia, which nearly always progress to AML. More recently, investigators noted that AML patients who achieved complete morphological remission after chemotherapy often have clonal hematopoiesis predominantly marked by either
<italic>DNMT3A</italic>
,
<italic>TET2</italic>
or
<italic>IDH1/2</italic>
mutations, which were also present at diagnosis of AML. This preleukemic clone represents involvement of an early hematopoietic stem cells, which is resistant to standard therapy. The same clonal hematopoietic mutations have been identified in older ‘normal' individuals who have a modest increased risk of developing frank AML. These individuals have occasionally been said, probably inappropriately, to have a preleukemia clone. Our evolving understanding of the term preleukemia has occurred by advancing technology including studies of X chromosome inactivation, cytogenetics and more recently deep nucleotide sequencing.</p>
</div>
</front>
<back>
<div1 type="bibliography">
<listBibl>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
<biblStruct></biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Leukemia</journal-id>
<journal-id journal-id-type="iso-abbrev">Leukemia</journal-id>
<journal-title-group>
<journal-title>Leukemia</journal-title>
</journal-title-group>
<issn pub-type="ppub">0887-6924</issn>
<issn pub-type="epub">1476-5551</issn>
<publisher>
<publisher-name>Nature Publishing Group</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">27899806</article-id>
<article-id pub-id-type="pmc">5339433</article-id>
<article-id pub-id-type="pii">leu2016364</article-id>
<article-id pub-id-type="doi">10.1038/leu.2016.364</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Preleukemia: one name, many meanings</article-title>
<alt-title alt-title-type="running">Preleukemia</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Koeffler</surname>
<given-names>H P</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="aff" rid="aff2">2</xref>
<xref ref-type="aff" rid="aff3">3</xref>
<xref ref-type="corresp" rid="caf1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Leong</surname>
<given-names>G</given-names>
</name>
<xref ref-type="aff" rid="aff2">2</xref>
</contrib>
<aff id="aff1">
<label>1</label>
<institution>Department of Hematology and Oncology, Cedars-Sinai Medical Center</institution>
, Los Angeles, CA,
<country>USA</country>
</aff>
<aff id="aff2">
<label>2</label>
<institution>Cancer Science Institute of Singapore, National University of Singapore</institution>
,
<country>Singapore</country>
</aff>
<aff id="aff3">
<label>3</label>
<institution>National University Cancer Institute of Singapore, National University Hospital</institution>
,
<country>Singapore</country>
</aff>
</contrib-group>
<author-notes>
<corresp id="caf1">
<label>*</label>
<institution>Cancer Science Institute of Singapore, National University of Singapore</institution>
. 14 Medical Drive, MD6, Centre for Translational Medicine, #12-01, Singapore 117599,
<country>Singapore</country>
. E-mail:
<email>phillip_koeffler@nuhs.edu.sg</email>
or
<email>H.Koeffler@cshs.org</email>
.</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>03</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epreprint">
<day>30</day>
<month>11</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>03</day>
<month>01</month>
<year>2017</year>
</pub-date>
<volume>31</volume>
<issue>3</issue>
<fpage>534</fpage>
<lpage>542</lpage>
<history>
<date date-type="received">
<day>31</day>
<month>05</month>
<year>2016</year>
</date>
<date date-type="rev-recd">
<day>11</day>
<month>11</month>
<year>2016</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>11</month>
<year>2016</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2017 The Author(s)</copyright-statement>
<copyright-year>2017</copyright-year>
<copyright-holder>The Author(s)</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/4.0/">
<pmc-comment>author-paid</pmc-comment>
<license-p>This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc-sa/4.0/">http://creativecommons.org/licenses/by-nc-sa/4.0/</ext-link>
</license-p>
</license>
</permissions>
<abstract>
<p>Definition of preleukemia has evolved. It was first used to describe the myelodysplastic syndrome (MDS) with a propensity to progress to acute myeloid leukemia (AML). Individuals with germline mutations of either
<italic>RUNX1</italic>
,
<italic>CEBPA</italic>
, or
<italic>GATA2</italic>
can also be called as preleukemic because they have a markedly increased incidence of evolution into AML. Also, alkylating chemotherapy or radiation can cause MDS/preleukemia, which nearly always progress to AML. More recently, investigators noted that AML patients who achieved complete morphological remission after chemotherapy often have clonal hematopoiesis predominantly marked by either
<italic>DNMT3A</italic>
,
<italic>TET2</italic>
or
<italic>IDH1/2</italic>
mutations, which were also present at diagnosis of AML. This preleukemic clone represents involvement of an early hematopoietic stem cells, which is resistant to standard therapy. The same clonal hematopoietic mutations have been identified in older ‘normal' individuals who have a modest increased risk of developing frank AML. These individuals have occasionally been said, probably inappropriately, to have a preleukemia clone. Our evolving understanding of the term preleukemia has occurred by advancing technology including studies of X chromosome inactivation, cytogenetics and more recently deep nucleotide sequencing.</p>
</abstract>
</article-meta>
</front>
<floats-group>
<fig id="fig1">
<label>Figure 1</label>
<caption>
<p>Schematic diagram of the hematopoietic tree with stem cells having a preleukemic mutation (
<italic>DNMT3A</italic>
) and blast cells acquiring a Driver (pan-AML) mutation (
<italic>NPM1</italic>
mutation), and retaining the
<italic>DNMT3A</italic>
mutations. Black dot,
<italic>DNMT3A</italic>
mutation; Red dot,
<italic>NPM1</italic>
mutation. Figure summarizes data by John Dick's lab.
<sup>
<xref ref-type="bibr" rid="bib93">93</xref>
</sup>
</p>
</caption>
<graphic xlink:href="leu2016364f1"></graphic>
</fig>
<fig id="fig2">
<label>Figure 2</label>
<caption>
<p>Evolution to MDS→secondary (s) AML (sAML)→remission and potential therapeutic intervention.</p>
</caption>
<graphic xlink:href="leu2016364f2"></graphic>
</fig>
<fig id="fig3">
<label>Figure 3</label>
<caption>
<p>Hematopoiesis: Normal elderly individual±evolution to sAML. Normal elderly individuals can develop clonal hemtopoiesis marked by a mutation in their early hematopoietic stem cells (HSC). Some of these individuals will develop myelodysplastic syndrome (MDS); and with the acquisition of a Driver mutation, they can develop secondary AML (sAML). These patients may go into complete morphologic remission but often retain their preleukemic clone. With relapse, they can either retain the original Driver mutation or acquire a new Driver mutation. Dotted line suggests that some normal elderly individuals with clonal hematopoiesis may develop MDS and sAML.</p>
</caption>
<graphic xlink:href="leu2016364f3"></graphic>
</fig>
<table-wrap id="tbl1">
<label>Table 1</label>
<caption>
<title>Exome sequencing: mutational defects in MDS and sAML versus
<italic>de novo</italic>
AML</title>
</caption>
<table frame="hsides" rules="groups" border="1">
<colgroup>
<col align="left"></col>
<col align="center"></col>
<col align="left"></col>
<col align="center"></col>
<col align="center"></col>
<col align="center"></col>
</colgroup>
<thead valign="bottom">
<tr>
<th colspan="2" align="center" valign="top" charoff="50">
<italic>MDS</italic>
<hr></hr>
</th>
<th colspan="2" align="center" valign="top" charoff="50">
<italic>sAML</italic>
<hr></hr>
</th>
<th colspan="2" align="center" valign="top" charoff="50">
<italic>De novo AML</italic>
<hr></hr>
</th>
</tr>
<tr>
<th align="left" valign="top" charoff="50">
<italic>Gene</italic>
</th>
<th align="center" valign="top" charoff="50">
<italic>Mutations (%)</italic>
</th>
<th align="left" valign="top" charoff="50">
<italic>Gene</italic>
</th>
<th align="center" valign="top" charoff="50">
<italic>Mutations (%)</italic>
</th>
<th align="center" valign="top" charoff="50">
<italic>Gene</italic>
</th>
<th align="center" valign="top" charoff="50">
<italic>Mutations (%)</italic>
</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left" valign="top" charoff="50">TET2
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">33</td>
<td align="left" valign="top" charoff="50">
<italic>TET2</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">20</td>
<td align="center" valign="top" charoff="50">FLT3
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">28</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">→SF3B1
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">32</td>
<td align="left" valign="top" charoff="50">
<italic>SF3B1</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">11</td>
<td align="center" valign="top" charoff="50">NPM1
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">27</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">ASXL1
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">23</td>
<td align="left" valign="top" charoff="50">
<italic>ASXL1</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">32</td>
<td align="center" valign="top" charoff="50">DNMT3A</td>
<td align="center" valign="top" charoff="50">26</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">→SRSF2
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">17</td>
<td align="left" valign="top" charoff="50">
<italic>SRSF2</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">20</td>
<td align="center" valign="top" charoff="50">IDH1/2</td>
<td align="center" valign="top" charoff="50">10</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">→ZRSR2
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">8</td>
<td align="left" valign="top" charoff="50">
<italic>ZRSR2</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">8</td>
<td align="center" valign="top" charoff="50">RUNX1
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">9</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">EZH2
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="left" valign="top" charoff="50">
<italic>EZH2</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">9</td>
<td align="center" valign="top" charoff="50">TET2</td>
<td align="center" valign="top" charoff="50">9</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">BCOR
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">4</td>
<td align="left" valign="top" charoff="50">
<italic>BCOR</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">8</td>
<td align="center" valign="top" charoff="50">NRAS/KRAS
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">8</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">→U2AF1
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">8</td>
<td align="left" valign="top" charoff="50">
<italic>U2AF1</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">16</td>
<td align="center" valign="top" charoff="50">TP53</td>
<td align="center" valign="top" charoff="50">8</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">STAG2
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">8</td>
<td align="left" valign="top" charoff="50">
<italic>STAG2</italic>
<xref ref-type="fn" rid="t1-fn2">a</xref>
</td>
<td align="center" valign="top" charoff="50">14</td>
<td align="center" valign="top" charoff="50">CEBPA
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">6</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">RUNX1</td>
<td align="center" valign="top" charoff="50">10</td>
<td align="left" valign="top" charoff="50">
<italic>RUNX1</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">31</td>
<td align="center" valign="top" charoff="50">WT1
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">6</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">DNMT3A</td>
<td align="center" valign="top" charoff="50">13</td>
<td align="left" valign="top" charoff="50">
<italic>NF1</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">6</td>
<td align="center" valign="top" charoff="50">PTPN11
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">5</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">IDH2/IDH1</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="left" valign="top" charoff="50">
<italic>NRAS/KRAS</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">31</td>
<td align="center" valign="top" charoff="50">KIT
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">4</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">TP53</td>
<td align="center" valign="top" charoff="50">6</td>
<td align="left" valign="top" charoff="50">
<italic>TP53</italic>
</td>
<td align="center" valign="top" charoff="50">15</td>
<td align="center" valign="top" charoff="50">U2AF1</td>
<td align="center" valign="top" charoff="50">4</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">FLT3</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="left" valign="top" charoff="50">
<italic>IDH1/2</italic>
</td>
<td align="center" valign="top" charoff="50">20</td>
<td align="center" valign="top" charoff="50">KRAS
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">4</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">CBL</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="left" valign="top" charoff="50">
<italic>FLT3</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">19</td>
<td align="center" valign="top" charoff="50">SMC1A</td>
<td align="center" valign="top" charoff="50">4</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">JAK2</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="left" valign="top" charoff="50">
<italic>DNMT3A</italic>
</td>
<td align="center" valign="top" charoff="50">19</td>
<td align="center" valign="top" charoff="50">SMC3</td>
<td align="center" valign="top" charoff="50">4</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">BCOR</td>
<td align="center" valign="top" charoff="50">3</td>
<td align="left" valign="top" charoff="50">
<italic>PTPN11</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="center" valign="top" charoff="50">PHF6</td>
<td align="center" valign="top" charoff="50">3</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">NRAS or KRAS</td>
<td align="center" valign="top" charoff="50">7</td>
<td align="left" valign="top" charoff="50">
<italic>CEBPA</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">3</td>
<td align="center" valign="top" charoff="50">STAG2</td>
<td align="center" valign="top" charoff="50">2</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">MPL</td>
<td align="center" valign="top" charoff="50">3</td>
<td align="left" valign="top" charoff="50">
<italic>NPM1</italic>
<xref ref-type="fn" rid="t1-fn3">b</xref>
</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="center" valign="top" charoff="50">RAD21</td>
<td align="center" valign="top" charoff="50">2</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">NF1</td>
<td align="center" valign="top" charoff="50">3</td>
<td align="left" valign="top" charoff="50">
<italic>SMC3</italic>
</td>
<td align="center" valign="top" charoff="50">2</td>
<td align="center" valign="top" charoff="50">FAM5C</td>
<td align="center" valign="top" charoff="50">2</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">ATM</td>
<td align="center" valign="top" charoff="50">3</td>
<td align="left" valign="top" charoff="50">
<italic>CBL</italic>
</td>
<td align="center" valign="top" charoff="50">5</td>
<td align="center" valign="top" charoff="50">EZH2</td>
<td align="center" valign="top" charoff="50">1</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="t1-fn1">
<p>→, mutant spliceosome gene; sAML, secondary AML (MDS→AML). MDS data;
<sup>
<xref ref-type="bibr" rid="bib9">9</xref>
</sup>
sAML data;
<sup>
<xref ref-type="bibr" rid="bib30">30</xref>
</sup>
de novo AML data.
<sup>
<xref ref-type="bibr" rid="bib26">26</xref>
</sup>
</p>
</fn>
<fn id="t1-fn2">
<label>a</label>
<p>Notable difference of incidence during MDS and sAML versus de novo AML.</p>
</fn>
<fn id="t1-fn3">
<label>b</label>
<p>Driver (Pan AML) mutations.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</pmc>
<affiliations>
<list>
<country>
<li>Singapour</li>
<li>États-Unis</li>
</country>
</list>
<tree>
<country name="États-Unis">
<noRegion>
<name sortKey="Koeffler, H P" sort="Koeffler, H P" uniqKey="Koeffler H" first="H P" last="Koeffler">H P Koeffler</name>
</noRegion>
</country>
<country name="Singapour">
<noRegion>
<name sortKey="Koeffler, H P" sort="Koeffler, H P" uniqKey="Koeffler H" first="H P" last="Koeffler">H P Koeffler</name>
</noRegion>
<name sortKey="Koeffler, H P" sort="Koeffler, H P" uniqKey="Koeffler H" first="H P" last="Koeffler">H P Koeffler</name>
<name sortKey="Leong, G" sort="Leong, G" uniqKey="Leong G" first="G" last="Leong">G. Leong</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Pmc/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000132 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Pmc/Checkpoint/biblio.hfd -nk 000132 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
   |flux=    Pmc
   |étape=   Checkpoint
   |type=    RBID
   |clé=     PMC:5339433
   |texte=   Preleukemia: one name, many meanings
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Checkpoint/RBID.i   -Sk "pubmed:27899806" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a LymphedemaV1 

Wicri

This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024