51. 135GC and 172GT polymorphism in the 5' untranslated region of RAD51 and sporadic endometrial cancer risk in Polish women
- Author
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Beata, Smolarz, Dariusz, Samulak, Magdalena, Michalska, Bożena, Góralczyk, Krzysztof, Szyłło, Jarosław, Lewy, Stanisław, Sporny, Grzegorz, Kokołaszwili, Marek, Burzyński, and Hanna, Romanowicz-Makowska
- Subjects
DNA, Neoplasm ,Adenocarcinoma ,Middle Aged ,Polymorphism, Single Nucleotide ,Endometrial Neoplasms ,Postmenopause ,Risk Factors ,Odds Ratio ,Humans ,Female ,Genetic Predisposition to Disease ,Poland ,Rad51 Recombinase ,5' Untranslated Regions - Abstract
Despite advanced diagnostic and therapeutic procedures, endometrial cancer (EC) is still responsible for high morbidity and mortality of women. The genetic variability in RAD51 may contribute to the appearance and progression of various cancers including EC.We investigated the association of polymorphisms in the DNA repair genes RAD51 135GC and 172GT with endometrial cancer risk.The genotypes of RAD51 135GC and 172GT polymorphism were determined by PCR-RFLP methods in endometrial tissue of 240 cancer subjects and 240 healthy subjects who served as controls.In the present work we demonstrated a significant positive association between the RAD51 C/C genotype and endometrial carcinoma, with an adjusted odds ratio (OR) of 13.0 (p0.0001). The distribution of genotypes for 135GC SNP in endometrial cancer patients vs. controls was: 10% vs. 27% for GG, 13% vs. 58% for GC and 77% vs. 15% for CC genotype, respectively. Variant 135C allele of RAD51 increased the cancer risk (OR = 1.81; 95% CI 0.11-2.93, p = 0.022). The higher risk of EC occurrence was associated with the combined C135C-G172T genotype (OR = 7.69; 95% CI 3.45-17.12).The results indicated that the polymorphism 135GC of the RAD51 gene may be positively associated with endometrial carcinoma in the Polish population. Further studies, conducted on a larger group, are required to clarify this point.
- Published
- 2011