[No authors listed]
Gene promoter methylation is a common epigenetic event, taking place in the early phase of tumorigenesis, which has a great potential as a diagnostic and prognostic cancer biomarker. In this umbrella review, we provide an overview on the association between gene-promoter methylation of protein-coding genes and cancer risk based on currently available meta-analyses data on gene promoter methylation. We searched MEDLINE via PubMed and the Cochrane Database of for meta-analyses that examine the association between gene-promoter methylation and cancer, published until January 2019 in English. We used AMSTAR to assess the quality of the included studies and applied a set of pre-specified criteria to evaluate the magnitude of each association. We provide a comprehensive overview of 80 unique combinations between 22 different genes and 18 cancer outcomes, all of which indicated a positive association between promoter hypermethylation and cancer. In total, the 70 meta-analyses produced significant results under a random-effects model with odds ratios that ranged from 1.94 to 26.60, with the summary effect being in favor of the unmethylated group in all cases. Three of the strong evidence associations involve RASSF1 methylation on bladder cancer risk (ORâ¯=â¯18.46; 95% CI: 12.69-26.85; I2â¯=â¯0%), MGMT methylation on NSCLC (ORâ¯=â¯4.25; 95% CI: 2.83-6.38; I2â¯=â¯22.4%) and RARB methylation on prostate cancer (ORâ¯=â¯6.87; 95% CI: 4.68-10.08; I2â¯=â¯0%). Meta-analyses showed a moderate quality, AMSTAR score ranging from 4 to 9 (Mdnâ¯=â¯8; IQR: 7.0 to 8.0). As primary studies and meta-analyses on the subject accumulate, more genetic loci may be found to be highly associated with specific cancer types and hence the biomarker sets will become wider.
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