Expression of the proliferating cell nuclear antigen and protein products of tumour suppressor genes in the human foetal testis

Tumour suppressor genes retinoblastoma (Rb1) and adenomatous polyposis coli (Apc) as well as the proliferating cell nuclear antigen (PCNA) are involved in embryonic development. The purpose of the present study was to investigate the expression of Rb1 protein, APC protein and PCNA during development...

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Published inAndrologia Vol. 36; no. 1; pp. 24 - 30
Main Authors Marić, S., Bulić-Jakuš, F., Ježek, D., Jurić-Lekić, G., Kos, M., Vlahović, M.
Format Journal Article
LanguageEnglish
Published Berlin, Germany Blackwell Verlag GmbH 01.02.2004
Blackwell
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Summary:Tumour suppressor genes retinoblastoma (Rb1) and adenomatous polyposis coli (Apc) as well as the proliferating cell nuclear antigen (PCNA) are involved in embryonic development. The purpose of the present study was to investigate the expression of Rb1 protein, APC protein and PCNA during development of the human foetal testis. Qualitative analysis of their expression at the single‐cell level was performed using immunohistochemistry on archive samples of the foetal testis (18–37 gestation week). Stereological parameters (volume density, absolute volume, numerical density, absolute number) were calculated for quantification of the overall expression of those proteins that were expressed frequently enough for such an analysis. PCNA was frequently expressed in nuclei of immature Sertoli cells and prospermatogonia and less frequently in surrounding peritubular (myoid) and interstitial cells. The pRb1 protein was present in nuclei of prospermatogonia and Sertoli cells but was absent from the interstitial tissue. APC protein was expressed in the cytoplasm of a very small number of prospermatogonia and interstitial (Leydig) cells. The overall expression of PCNA in all stages of development was higher than pRb1 expression.
Bibliography:ark:/67375/WNG-K2ZV83ZK-R
ArticleID:AND597
istex:B8BA0BADA45C325560A352A754785D3886E1EAC8
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0303-4569
1439-0272
DOI:10.1046/j.1439-0272.2003.00597.x