Differential expression of p73 splice variants and protein in benign and malignant ovarian tumours

The p73 gene encodes a protein with substantial structural and functional similarities to the tumour-suppressor p53. Alternative splicing of p73 mRNA leads to expression of 6 known RNA species and proteins ( alpha , beta , gamma , delta , epsilon , zeta ). We analysed the expression of these splice...

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Veröffentlicht in:International journal of cancer 2000-10, Vol.88 (1), p.66-70
Hauptverfasser: Zwahlen, D, Tschan, M P, Grob, T J, Peters, U R, Fink, D, Haenggi, W, Altermatt, HJ, Cajot, J-F, Tobler, A, Fey, M F, Aebi, S
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Sprache:eng
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Zusammenfassung:The p73 gene encodes a protein with substantial structural and functional similarities to the tumour-suppressor p53. Alternative splicing of p73 mRNA leads to expression of 6 known RNA species and proteins ( alpha , beta , gamma , delta , epsilon , zeta ). We analysed the expression of these splice variants in ovarian adenocarcinoma by RT-PCR followed by detection of amplicons with the Southern technique and by immunoblot in 32 malignant and benign epithelial ovarian tumour specimens and 3 ovarian adenocarcinoma cell lines (A2780, 2008, OVCAR-3). p73 alpha mRNA was expressed in all 17 ovarian cancer specimens, and 14 of 17 expressed at least 3 splice variants. In contrast, a different expression pattern was present in the ovarian adenomas: p73 alpha was detected in 6 of 12 benign tumours, and only 1 adenoma expressed 3 splice variants. p73 protein was expressed in 9 of 16 ovarian cancer specimens, in all cell lines and in 1 of 3 borderline tumours. In contrast, none of 9 ovarian adenomas expressed detectable amounts of p73 protein. Expression of p73 mRNA and protein was not correlated with FIGO stage and histological grade, but we observed a significant correlation with over-expression of p53 protein. In summary, epithelial ovarian cancers express a more complex p73 isoform pattern and higher levels of p73 mRNA and protein than ovarian adenomas.
ISSN:0020-7136
DOI:10.1002/1097-0215(20001001)88:1<66::AID-IJC10>3.3.CO;2-P