Literature DB >> 24535941

Functional polymorphisms in apoptosis pathway genes and survival in patients with gastric cancer.

Dongying Gu1, Mulong Du, Cuiju Tang, Haiyan Chu, Zhi Xu, Xinyin Huo, Weida Gong, Yongfei Tang, Jianwei Zhou, Na Tong, Yong Xu, Zhengdong Zhang, Meilin Wang, Jinfei Chen.   

Abstract

The FAS, FAS ligand (FASL), and CASP8 are key regulators for apoptosis and their deregulations play an important role in carcinogenesis. However, the effects of promoter polymorphisms of the FAS, and FASL, and CASP8 genes on the survival of gastric cancer are unknown. In this study, we investigated the association of four polymorphisms (FAS -1377G>A, -670A>G, FASL -844C>T, and CASP8 -652 6N ins>del) with the clinical outcome of 940 gastric cancer patients in a Chinese population. The correlation between genotype and survival outcomes was assessed by the Kaplan-Meier method, Cox proportional hazards models and the log-rank test. Our results revealed that individuals with CASP8 -652 6N ins/del+del/del genotypes had a decreased risk of death compared with those with ins/ins genotype (log-rank P=0.005; hazard ratio=0.75, 95% confidence interval=0.62-0.92). The protective effect of the del allele was further confirmed in subgroups of patients with tumor size ≤ 5 cm (0.66, 0.50-0.86) and T2 depth invasion (0.59, 0.37-0.94), but no significant association was observed in the subgroups of lymph node metastasis (0.67, 0.47-0.97), and distance metastasis (0.73, 0.60-0.90). Our findings suggest that, if validated in different independent populations, the CASP8 -652 6N ins>del polymorphism may serve as a promising genetic marker for gastric cancer prognosis.
Copyright © 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  CASP8; FAS/FASL; apoptosis; gastric cancer survival; single-nucleotide polymorphisms

Mesh:

Substances:

Year:  2014        PMID: 24535941     DOI: 10.1002/em.21856

Source DB:  PubMed          Journal:  Environ Mol Mutagen        ISSN: 0893-6692            Impact factor:   3.216


  4 in total

1.  Association of FAS A-670G Polymorphism and Risk of Uterine Leiomyoma in a Southeast Iranian Population.

Authors:  Abbas Mohammadpour-Gharehbagh; Saeedeh Salimi; Farshid Keshavarzi; Sepideh Zakerian; Mojtaba Sajadian; Mojgan Mokhtari
Journal:  Rep Biochem Mol Biol       Date:  2016-10

2.  FAS rs2234767 and rs1800682 polymorphisms jointly contributed to risk of colorectal cancer by affecting SP1/STAT1 complex recruitment to chromatin.

Authors:  Shizhi Wang; Shenshen Wu; Qingtao Meng; Xiaobo Li; Jinchun Zhang; Rui Chen; Meilin Wang
Journal:  Sci Rep       Date:  2016-01-13       Impact factor: 4.379

3.  Association of caspase 8 polymorphisms -652 6N InsDel and Asp302His with progression-free survival and tumor infiltrating lymphocytes in early breast cancer.

Authors:  Jan Dominik Kuhlmann; Hagen Sjard Bachmann; Theresa Link; Pauline Wimberger; Eric Kröber; Christoph Thomssen; Brahima Mallé; Daniel Bethmann; Martina Vetter; Eva Johanna Kantelhardt
Journal:  Sci Rep       Date:  2019-08-29       Impact factor: 4.379

4.  Prognostic relevance of caspase 8 -652 6N InsDel and Asp302His polymorphisms for breast cancer.

Authors:  J D Kuhlmann; A Bankfalvi; K W Schmid; R Callies; R Kimmig; P Wimberger; W Siffert; H S Bachmann
Journal:  BMC Cancer       Date:  2016-08-09       Impact factor: 4.430

  4 in total

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