Promoter Hypermethylation of Tumour Suppressor Genes as Potential Biomarkers in Colorectal Cancer

作者：Ng, Jennifer Mun-Kar; Yu, Jun^*

来源：International Journal of Molecular Sciences, 2015, 16(2): 2472-2496.

DOI：10.3390/ijms16022472

• ISLAND METHYLATOR PHENOTYPE
• MOLECULAR PATHOLOGICAL EPIDEMIOLOGY
• DNA METHYLTRANSFERASES 3A
• FECAL DNA
• CPG METHYLATION
• STOOL DNA
• LINE-1 HYPOMETHYLATION
• TRANSCRIPTION FACTOR
• COLON-CANCER
• MICROSATELLITE INSTABILITY

Colorectal cancer (CRC) is a common malignancy and the fourth leading cause of cancer deaths worldwide. It results from the accumulation of multiple genetic and epigenetic changes leading to the transformation of colon epithelial cells into invasive adenocarcinomas. In CRC, epigenetic changes, in particular promoter CpG island methylation, occur more frequently than genetic mutations. Hypermethylation contributes to carcinogenesis by inducing transcriptional silencing or downregulation of tumour suppressor genes and currently, over 600 candidate hypermethylated genes have been identified. Over the past decade, a deeper understanding of epigenetics coupled with technological advances have hinted at the potential of translating benchtop research into biomarkers for clinical use. DNA methylation represents one of the largest bodies of literature in epigenetics, and hence has the highest potential for minimally invasive biomarker development. Most progress has been made in the development of diagnostic markers and there are currently two, one stool-based and one blood-based, biomarkers that are commercially available for diagnostics. Prognostic and predictive methylation markers are still at their infantile stages.

• 出版日期2015-2
• 单位香港中文大学深圳研究院