Genetic variations in apoptosis pathway and the risk of ovarian cancer

Hui Xie, Wade Tao, Xifeng Wu, Jian Gu

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Background: Apoptosis is a highly conserved form of cell death and aberrant regulation of apoptotic cell death mechanisms leads to variety of major human diseases, especially tumor formation. Genetic variations in apoptosis genes may increase susceptibility to ovarian cancer. Results: In individual SNP analysis, 12 SNPs in 5 apoptosis pathway genes were significantly associated with ovarian cancer risk after adjustment for multiple comparisons at q-value <0.05. The most significant SNP was rs11152377 in the Bcl- 2 gene. The homozygous variant TT genotype was associated with a significantly decreased risk of ovarian cancer (odds ratio [OR] =0.53; 95% confidence interval [CI], 0.37-0.77, P<0.001). Cumulative effect analysis showed joint effects of increased risk of ovarian cancer with increasing number of unfavorable genotypes in patients. Classification and regression tree (CART) analysis further revealed high-order genegene interactions and categorized the study subjects into low-, medium-, and highrisk groups. Compared with the low-risk group, medium-risk group and high-risk group conferred 1.76-fold (95% CI: 1.06-2.90) and 3.64-fold (95% CI: 2.37-5.59) increased risk of ovarian cancer (P for trend <0.001) Materials and Methods: In a case-control study of 417 ovarian cancer patients and 417 matched controls, we evaluated the associations of 587 single nucleotide polymorphisms (SNPs) from 65 genes of the apoptosis pathway with the risk of ovarian cancer. Conclusions: Our results suggest that genetic variations in apoptosis pathway genes modulate the risk of ovarian cancer individually and jointly.

Original languageEnglish (US)
Pages (from-to)56737-56745
Number of pages9
JournalOncotarget
Volume7
Issue number35
DOIs
StatePublished - 2016

Keywords

  • Apoptosis pathway
  • Ovarian cancer
  • Risk
  • Single nucleotide polymorphism

ASJC Scopus subject areas

  • Oncology

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