| Literature DB >> 18677302 |
Richard J Flavin1, Paul C Smyth, Alexandros Laios, Sharon A O'Toole, Ciara Barrett, Stephen P Finn, Susan Russell, Martina Ring, Karen M Denning, Jinghuan Li, Sinead T Aherne, Dania A Sammarae, Natasha A Aziz, Araibi Alhadi, Brian L Sheppard, Kai Lao, Orla M Sheils, John J O'Leary.
Abstract
MicroRNAs are a group of small non-coding RNAs approximately 22 nucleotides in length. Recent work has shown differential expression of mature microRNAs in human cancers. We characterized the alteration in expression of a select group of microRNAs in primary peritoneal carcinoma relative to matched cases of ovarian serous carcinoma. MicroRNA expression was analysed using semi-quantitative stem-loop RT-PCR on a set of 34 formalin-fixed paraffin-embedded samples. Protein expression of p53 and bcl-2 was quantified in the corresponding tissue microarray. We provide definitive evidence that there is downregulation of a select group of microRNAs in tumours meeting Gynaecological Oncology Group criteria for primary peritoneal carcinoma relative to ovarian serous carcinoma. Specifically, we show decreased p53 expression and downregulation of miR-195 and miR-497 from the microRNA cluster site at chromosome 17p13.1 in primary peritoneal carcinoma relative to ovarian serous carcinoma. miR-195 and miR-497 may have potential roles as tumour-suppressor genes in primary peritoneal tumourigenesis.Entities:
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Year: 2008 PMID: 18677302 DOI: 10.1038/modpathol.2008.135
Source DB: PubMed Journal: Mod Pathol ISSN: 0893-3952 Impact factor: 7.842