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Association between PLCE1 rs2274223 A > G polymorphism and cancer risk: proof from a meta-analysis
Wenji Xue1, Meiling Zhu1, Yiwei Wang1
1Department of Oncology, Xin Hua Hospital affiliated To Shanghai Jiaotong University School of Medicine, Shanghai 200092, Shanghai, China.
The Phospholipase C epsilon 1 (PLCE1) rs2274223 A > G polymorphism is linked to a higher risk of overall cancer, particularly esophageal squamous cell carcinoma (ESCC). Further research is needed to confirm these findings due to study heterogeneity.
Area of Science:
- Genetics and Molecular Biology
- Cancer Research
- Epidemiology
Background:
- Phospholipase C epsilon 1 (PLCE1) is implicated in cell growth, differentiation, and oncogenesis.
- Previous studies on the association between PLCE1 rs2274223 polymorphism and cancer risk have yielded inconclusive results.
- A comprehensive meta-analysis is required to consolidate existing evidence and clarify the role of this polymorphism in cancer susceptibility.
Purpose of the Study:
- To conduct a meta-analysis evaluating the association between the PLCE1 rs2274223 A > G polymorphism and cancer risk.
- To investigate potential associations in specific cancer types, such as esophageal squamous cell carcinoma (ESCC) and gastric cancer (GC).
- To explore subgroup variations based on ethnicity, study quality, sample size, and Hardy-Weinberg equilibrium (HWE).
Main Methods:
- A meta-analysis was performed on data from 22 studies, encompassing 13188 cancer cases and 14666 controls.
- Pooled odds ratios (OR) and 95% confidence intervals (CI) were calculated for various genetic models (e.g., G vs. A, GG vs. AA, GA vs. AA, GG/GA vs. AA).
- Stratification analyses were conducted to examine associations within specific subgroups and cancer types.
Main Results:
- The PLCE1 rs2274223 A > G polymorphism was associated with an increased risk of overall cancer.
- Significant associations were observed for ESCC but not for GC.
- The polymorphism showed a stronger association with ESCC risk among Asian subgroups, studies with high quality scores, larger sample sizes (>1000), and those consistent with HWE.
Conclusions:
- The PLCE1 rs2274223 A > G polymorphism may contribute to increased cancer susceptibility, particularly for ESCC.
- The findings suggest a potential role for PLCE1 in the development of esophageal cancer.
- Substantial heterogeneity across studies necessitates further investigation to definitively confirm these associations and their clinical implications.
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