Ishioka Chikashi
Department of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
JR Sendai Hospital, Sendai, Japan.
JMA J. 2025 Jul 15;8(3):703-707. doi: 10.31662/jmaj.2025-0074. Epub 2025 Jun 13.
Epigenetic regulation mechanisms such as deoxy ribonucleic acid (DNA) methylation are important for controlling various biological phenomena by regulating gene expression at the genome level. Epigenetic abnormalities are associated with the onset of diseases including cancers. Aberrant DNA methylation is an important epigenetic change in the development and progression of colorectal cancer. DNA methylation in tumor tissues occurs mainly in CpG islands in the promoter regions of genes and inactivates gene functions by negatively suppressing transcription. The CpG island methylator phenotype (CIMP) is an important carcinogenic mechanism in colorectal cancer related to DNA methylation and is involved in approximately 20% of all colorectal cancers. However, CIMP does not always represent the genome-wide DNA methylation status in colorectal cancer. We developed a new method to assess genome-wide DNA methylation status and showed that it is a predictor of the efficacy of anti-estimated glomerular filtration rate (EGFR) antibody drugs and a prognostic factor. This new method has received regulatory approval as a new in vitro diagnostic for predicting sensitivity to anti-EGFR antibody drugs in colorectal cancer.
诸如脱氧核糖核酸(DNA)甲基化等表观遗传调控机制,通过在基因组水平调控基因表达,对于控制各种生物学现象至关重要。表观遗传异常与包括癌症在内的多种疾病的发生有关。异常的DNA甲基化是结直肠癌发生和发展过程中的一种重要表观遗传变化。肿瘤组织中的DNA甲基化主要发生在基因启动子区域的CpG岛,通过负向抑制转录使基因功能失活。CpG岛甲基化表型(CIMP)是结直肠癌中与DNA甲基化相关的一种重要致癌机制,约占所有结直肠癌的20%。然而,CIMP并不总是代表结直肠癌中全基因组的DNA甲基化状态。我们开发了一种评估全基因组DNA甲基化状态的新方法,并表明它是抗表皮生长因子受体(EGFR)抗体药物疗效的预测指标和一个预后因素。这种新方法已获得监管批准,作为一种预测结直肠癌对抗EGFR抗体药物敏感性的新型体外诊断方法。