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Expression screening of cancer/testis genes in prostate cancer identifies nr6a1 as a novel marker of disease progression and aggressiveness

Identifieur interne : 000E64 ( Istex/Corpus ); précédent : 000E63; suivant : 000E65

Expression screening of cancer/testis genes in prostate cancer identifies nr6a1 as a novel marker of disease progression and aggressiveness

Auteurs : Romain Mathieu ; Bertrand Evrard ; Gaëlle Fromont ; Nathalie Rioux-Leclercq ; Julie Godet ; Xavier Cathelineau ; François Guillé ; Michael Primig ; Frédéric Chalmel

Source :

RBID : ISTEX:6636028DAD7073A903B1AA8F93CFB8DD8ED432B5

English descriptors

Abstract

Cancer/Testis (CT) genes are expressed in male gonads, repressed in most healthy somatic tissues and de‐repressed in various somatic malignancies including prostate cancers (PCa). Because of their specific expression signature and their associations with tumor aggressiveness and poor outcomes, CT genes are considered to be useful biomarkers and they are also targets for the development of new anti‐cancer immunotherapies. The aim of this study was to identify novel CT genes associated with hormone‐sensitive prostate cancer (HSPC), and castration‐resistant prostate cancer (CRPC).

Url:
DOI: 10.1002/pros.22659

Links to Exploration step

ISTEX:6636028DAD7073A903B1AA8F93CFB8DD8ED432B5

Le document en format XML

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<affiliation>Centre d'étude et de Recherche sur les Pathologies Prostatiques, Paris, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Nathalie</namePart>
<namePart type="family">Rioux‐Leclercq</namePart>
<affiliation>Service d'Anatomie et Cytologie Pathologiques, CHU/Université de Rennes, Rennes, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Julie</namePart>
<namePart type="family">Godet</namePart>
<affiliation>Département d'Anatomocytopathologie, CHU/Université de Poitiers, Poitiers, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Xavier</namePart>
<namePart type="family">Cathelineau</namePart>
<affiliation>Institut Mutualiste Montsouris, Paris, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">François</namePart>
<namePart type="family">Guillé</namePart>
<affiliation>Département d'Urologie, CHU de Rennes, Rennes, France</affiliation>
<affiliation>Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Michael</namePart>
<namePart type="family">Primig</namePart>
<affiliation>Inserm Unité 1085‐Irset, Université de Rennes 1, Rennes, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Frédéric</namePart>
<namePart type="family">Chalmel</namePart>
<affiliation>Inserm Unité 1085‐Irset, Université de Rennes 1, Rennes, France</affiliation>
<affiliation>Inserm Unité 1085‐Irset, Université de Rennes 1, Rennes F‐35042, France.</affiliation>
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<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<place>
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</place>
<dateIssued encoding="w3cdtf">2013-07</dateIssued>
<dateCaptured encoding="w3cdtf">2012-11-23</dateCaptured>
<dateValid encoding="w3cdtf">2013-02-10</dateValid>
<copyrightDate encoding="w3cdtf">2013</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract>Cancer/Testis (CT) genes are expressed in male gonads, repressed in most healthy somatic tissues and de‐repressed in various somatic malignancies including prostate cancers (PCa). Because of their specific expression signature and their associations with tumor aggressiveness and poor outcomes, CT genes are considered to be useful biomarkers and they are also targets for the development of new anti‐cancer immunotherapies. The aim of this study was to identify novel CT genes associated with hormone‐sensitive prostate cancer (HSPC), and castration‐resistant prostate cancer (CRPC).</abstract>
<abstract>To identify novel CT genes we screened genes for which transcripts were detected by RNA profiling specifically in normal testis and in either HSPC or CRPC as compared to normal prostate and 44 other healthy tissues using GeneChips. The expression and clinicopathological significance of a promising candidate—NR6A1—was examined in HSPC, CRPC, and metastatic site samples using tissue microarrays.</abstract>
<abstract>We report the identification of 98 genes detected in CRPC, HSPC and testicular samples but not in the normal controls. Among them, cellular levels of NR6A1 were found to be higher in HSPC compared to normal prostate and further increased in metastatic lesions and CRPC. Furthermore, increased NR6A1 immunoreactivity was significantly associated with a high Gleason score, advanced pT stage and cancer cell proliferation.</abstract>
<abstract>Our results show that cellular levels of NR6A1 are correlated with disease progression in PCa. We suggest that this essential orphan nuclear receptor is a potential therapeutic target as well as a biomarker of PCa aggressiveness. Prostate 73: 1103–1114, 2013. © 2013 Wiley Periodicals, Inc.</abstract>
<note type="content">*Michael Primig and Frédéric Chalmel contributed equally to this work.</note>
<note type="content">*The authors declare no potential conflicts of interest.</note>
<note type="funding">ARTP Fellowship</note>
<note type="funding">ARC - No. 7985; </note>
<note type="funding">Inserm Avenir - No. R07216NS; </note>
<subject lang="en">
<genre>keywords</genre>
<topic>Cancer/Testis genes</topic>
<topic>castration‐resistant prostate cancer</topic>
<topic>biomarker</topic>
<topic>NR6A1</topic>
<topic>nuclear receptor</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>The Prostate</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Prostate</title>
</titleInfo>
<genre type="journal">journal</genre>
<note type="content"> Additional Supporting Information may be found in the online version of this article.Supporting Info Item: Supplemental File 1 - Supplemental File 2 - Supplemental File 3 - </note>
<subject>
<genre>article-category</genre>
<topic>Original Article</topic>
</subject>
<identifier type="ISSN">0270-4137</identifier>
<identifier type="eISSN">1097-0045</identifier>
<identifier type="DOI">10.1002/(ISSN)1097-0045</identifier>
<identifier type="PublisherID">PROS</identifier>
<part>
<date>2013</date>
<detail type="volume">
<caption>vol.</caption>
<number>73</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>10</number>
</detail>
<extent unit="pages">
<start>1103</start>
<end>1114</end>
<total>12</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">6636028DAD7073A903B1AA8F93CFB8DD8ED432B5</identifier>
<identifier type="DOI">10.1002/pros.22659</identifier>
<identifier type="ArticleID">PROS22659</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2013 Wiley Periodicals, Inc.</accessCondition>
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