Serveur d'exploration Hippolyte Bernheim

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Genome-Wide High-Resolution aCGH Analysis of Gestational Choriocarcinomas

Identifieur interne : 000166 ( Main/Exploration ); précédent : 000165; suivant : 000167

Genome-Wide High-Resolution aCGH Analysis of Gestational Choriocarcinomas

Auteurs : Henriette Poaty [France] ; Philippe Coullin [France] ; Jean Félix Peko ; Philippe Dessen [France] ; Ange Lucien Diatta [Sénégal] ; Alexander Valent [France] ; Eric Leguern [France] ; Sophie Prévot [France] ; Charles Gombé-Mbalawa ; Jean-Jacques Candelier [France] ; Jean-Yves Picard [France] ; Alain Bernheim [France]

Source :

RBID : PMC:3253784

Abstract

Eleven samples of DNA from choriocarcinomas were studied by high resolution CGH-array 244 K. They were studied after histopathological confirmation of the diagnosis, of the androgenic etiology and after a microsatellite marker analysis confirming the absence of contamination of tumor DNA from maternal DNA. Three cell lines, BeWo, JAR, JEG were also studied by this high resolution pangenomic technique. According to aCGH analysis, the de novo choriocarcinomas exhibited simple chromosomal rearrangements or normal profiles. The cell lines showed various and complex chromosomal aberrations. 23 Minimal Critical Regions were defined that allowed us to list the genes that were potentially implicated. Among them, unusually high numbers of microRNA clusters and imprinted genes were observed.


Url:
DOI: 10.1371/journal.pone.0029426
PubMed: 22253721
PubMed Central: 3253784


Affiliations:


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Le document en format XML

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<name sortKey="Picard, Jean Yves" sort="Picard, Jean Yves" uniqKey="Picard J" first="Jean-Yves" last="Picard">Jean-Yves Picard</name>
<affiliation wicri:level="4">
<nlm:aff id="aff2">
<addr-line>Université Paris XI, Paris Sud, Orsay, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>Université Paris XI, Paris Sud, Orsay</wicri:regionArea>
<placeName>
<settlement type="city">Orsay</settlement>
</placeName>
<orgName type="university">Université Paris-Sud</orgName>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff3">
<addr-line>INSERM U782, Endocrinologie et génétique de la reproduction et du développement, Clamart, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INSERM U782, Endocrinologie et génétique de la reproduction et du développement, Clamart</wicri:regionArea>
<wicri:noRegion>Clamart</wicri:noRegion>
<wicri:noRegion>Clamart</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Bernheim, Alain" sort="Bernheim, Alain" uniqKey="Bernheim A" first="Alain" last="Bernheim">Alain Bernheim</name>
<affiliation wicri:level="1">
<nlm:aff id="aff1">
<addr-line>INSERM U985, Institut Gustave Roussy, Villejuif, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INSERM U985, Institut Gustave Roussy, Villejuif</wicri:regionArea>
<wicri:noRegion>Villejuif</wicri:noRegion>
<wicri:noRegion>Villejuif</wicri:noRegion>
</affiliation>
<affiliation wicri:level="4">
<nlm:aff id="aff2">
<addr-line>Université Paris XI, Paris Sud, Orsay, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>Université Paris XI, Paris Sud, Orsay</wicri:regionArea>
<placeName>
<settlement type="city">Orsay</settlement>
</placeName>
<orgName type="university">Université Paris-Sud</orgName>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff6">
<addr-line>Molecular Pathology, Institut Gustave Roussy, Villejuif, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>Molecular Pathology, Institut Gustave Roussy, Villejuif</wicri:regionArea>
<wicri:noRegion>Villejuif</wicri:noRegion>
<wicri:noRegion>Villejuif</wicri:noRegion>
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</analytic>
<series>
<title level="j">PLoS ONE</title>
<idno type="eISSN">1932-6203</idno>
<imprint>
<date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Eleven samples of DNA from choriocarcinomas were studied by high resolution CGH-array 244 K. They were studied after histopathological confirmation of the diagnosis, of the androgenic etiology and after a microsatellite marker analysis confirming the absence of contamination of tumor DNA from maternal DNA. Three cell lines, BeWo, JAR, JEG were also studied by this high resolution pangenomic technique. According to aCGH analysis, the
<italic>de novo</italic>
choriocarcinomas exhibited simple chromosomal rearrangements or normal profiles. The cell lines showed various and complex chromosomal aberrations. 23 Minimal Critical Regions were defined that allowed us to list the genes that were potentially implicated. Among them, unusually high numbers of microRNA clusters and imprinted genes were observed.</p>
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<li>Sénégal</li>
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<region>
<li>Île-de-France</li>
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<name sortKey="Bernheim, Alain" sort="Bernheim, Alain" uniqKey="Bernheim A" first="Alain" last="Bernheim">Alain Bernheim</name>
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<name sortKey="Dessen, Philippe" sort="Dessen, Philippe" uniqKey="Dessen P" first="Philippe" last="Dessen">Philippe Dessen</name>
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}}

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HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:22253721" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a BernheimV1 

Wicri

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