Meng Kuang1, Wei Xu1, Chunxiang Cao1, Lili Shen1, Xunlei Zhang2, Juan Chang3, Jinfei Chen1, Tangcui Jun1
1Department of Oncology,
Nanjing First Hospital, 2Department of Oncology,
Nantong Tumor Hospital, 3Department of Oncology,
Taixing people’s Hospital
Objective:Breast cancer (BC) is the most widespread
cause of cancer-related death among women. Many published studies have assessed
the association between Glutathione S-transferase P1 (GSTP1) rs1695 polymorphism
and BC risk. However, whether GSTP1 rs1695 polymorphism could influence BC risk
has been controversial. So we performed this meta-analysis to pursue a more comprehensive
estimation of the association. Method: The electronic literature PUBMED
was searched using the search terms: “rs1695”, “GSTP1”, “polymorphism” and
“breast cancer” to look up all relevant articles. The search was limited to
English language papers. Additionally, a hand search of references of original
studies was used on this topic in order to identify additional studies. Studies
which were satisfied to the following criteria were included in our
meta-analysis: (a) performed a case–control studies, (b) contained available
genotype frequencies for both patients and control populations or provided OR
and 95% CI of relevant genetic models, (c) evaluation of the GSTP1 rs1695 polymorphism
and breast cancer risk. Result: In total, 36 case–control trails
including 20,615 cases and 20,481 controls were selected in our study. The primary
features of these included studies are shown in Table1. Among these eligible publications,
there were 21 studies from Europe, 12 from Asian and 2 from Africa and 3 of
mixed people. There were ten studies of premenopausal women and 13 studies of postmenopausal
women, While, 15 of them are hospital-based studies and 19 studies are population-based.Conclusion: In summary, our meta-analysis suggests that GSTP1 rs1695
A>G increase breast cancer risk in Asians. Understanding the components of
CEMP molecular links may provide an avenue for preventive and therapeutic
strategies to reduce cancer risk and mortality. Further investigations are
needed to characterize the association of GSTP1 A>G polymorphism with breast
cancer risk, and more original studies should be investigated to verify our
result in the future.
Key
Words: GSTP1
Polymorphism Breast cancer
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