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The CYP19A1 (TTTA)n Repeat Polymorphism May Affect the Prostate Cancer Risk: Evidence from a Meta-Analysis
Lei Guo1, Yanan Liu1, Lijun Liu2
1Department of Urology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
American Journal of Men'S Health
|May 26, 2021
Summary
The CYP19A1 (TTTA)n repeat polymorphism, specifically the 8-repeat allele, is linked to increased prostate cancer (PCa) risk. However, the CYP19A1 Arg264Cys polymorphism shows no association with PCa development.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Abnormal aromatase (CYP19A1) expression is implicated in prostate cancer (PCa) development.
- Previous studies on CYP19A1 gene polymorphisms and PCa risk have yielded conflicting results.
Purpose of the Study:
- To systematically evaluate the association between two CYP19A1 gene polymorphisms (Arg264Cys and (TTTA)n repeat) and PCa risk.
- To clarify the conflicting findings regarding CYP19A1 polymorphisms and their role in PCa carcinogenesis.
Main Methods:
- A comprehensive meta-analysis of eligible studies identified through searches of PubMed, EmBase, ScienceDirect, and Cochrane Library.
- Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated for the Arg264Cys polymorphism under various genetic models.
- The (TTTA)n repeat polymorphism was analyzed by considering specific repeat numbers as the minor allele in an allelic model.
Main Results:
- The CYP19A1 Arg264Cys polymorphism was not associated with PCa risk in the overall population, Caucasian, or Asian subgroups.
- The 8-repeat allele of the CYP19A1 (TTTA)n repeat polymorphism was significantly associated with an increased risk of PCa in the overall population.
- This increased risk was also observed in subgroups with population-based (PB) controls and those using capillary electrophoresis for genotyping.
Conclusions:
- The CYP19A1 (TTTA)n repeat polymorphism, particularly the 8-repeat allele, may influence prostate cancer risk.
- The CYP19A1 Arg264Cys polymorphism does not appear to be a significant risk factor for prostate cancer.
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