[No authors listed]
We conducted the present meta-analysis of relevant cohort studies to evaluate whether promoter methylation of the high in normal-1 (HIN-1) gene contributes to breast cancer. The MEDLINE (1966â~â2013), Cochrane Library (Issue 12, 2013), EMBASE (1980â~â2013), CINAHL (1982â~â2013), Web of Science (1945â~â2013), and Chinese Biomedical (CBM) (1982â~â2013) databases were searched without any language restrictions. Meta-analyses were conducted using Stata software (version 12.0; Stata Corporation, College Station, TX, USA). Crude odds ratios (ORs) with their 95 % confidence interval (CI) were calculated. Nine clinical cohort studies that enrolled a total of 693 breast cancer patients were included in the meta-analysis. The results of our meta-analysis demonstrated that HIN-1 methylation frequency in cancer tissue was significantly higher than that of normal and benign tissues (cancer tissue vs. normal tissue: ORâ=â52.60, 95 % CIâ=â33.77â~â81.92, Pâ<â0.001; cancer tissue vs. benign tissue: ORâ=â2.38, 95 % CIâ=â1.53â~â3.70, Pâ<â0.001; respectively). Ethnicity-stratified analysis indicated that HIN-1 promoter methylation was correlated with the pathogenesis of breast cancer among both Asians and Caucasians (all Pâ<â0.05). Our findings provide empirical evidence that aberrant HIN-1 promoter methylation may contribute to the pathogenesis of breast cancer. Thus, aberrant HIN-1 promoter methylation could be an independent and important biomarker used in predicting the prognosis and progression of breast cancer.
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