| Literature DB >> 32910383 |
T M Zavarykina1, A S Tyulyandina2, S V Khokhlova3, G N Khabas3, A V Asaturova3, Yu A Nosova3, P K Brenner4, M A Kapralova4,5, M V Atkarskaya4, D S Khodyrev6, A M Burdennyi4, V I Loginov7, M B Stenina2, G T Sukhikh3.
Abstract
We studied the association of polymorphic markers of cell cycle control genes (Arg72Pro of the TP53 gene, T(-410)G of the MDM2 gene, and Ser31Arg of the CDKN1A gene) in ovarian cancer and progression-free survival following platinum-based chemotherapy. Tumor tissue samples obtained from 49 patients who had undergone chemotherapy were examined. Patients received standard platinum-based chemotherapy and were observed until disease progression. Polymorphic markers of genes were evaluated by PCR-RFLP and real-time PCR. In patients carrying the G allele of the T(-410)G marker of the MDM2 gene, a decreasing trend was observed in median progression-free survival. An increase in the median progression-free survival was observed in carriers of the Pro allele of the TP53 gene (p=0.045). Furthermore, a stronger association was noted with carriers of the minor Pro/Pro homozygous genotype relative to the Arg/Arg genotype (p=0.007). In the subgroup of patients who underwent optimal or complete cytoreductive surgery, carriage of the minor Arg allele of the Ser31Arg marker (CDN1A gene) was associated with a decrease in the median progression-free survival time (p=0.004).Entities:
Keywords: cell cycle control; ovarian cancer; platinum-based chemotherapy; polymorphic marker; progression-free survival
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Year: 2020 PMID: 32910383 DOI: 10.1007/s10517-020-04915-5
Source DB: PubMed Journal: Bull Exp Biol Med ISSN: 0007-4888 Impact factor: 0.804