Department of Precision Medicine University of Campania "L. Vanvitelli", 80131 Naples, Italy.
Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Istituto di Endocrinologia ed Oncologia Sperimentale del C.N.R., Università Federico II, 80131 Napoli, Italy.
Biomolecules. 2020 Mar 13;10(3):446. doi: 10.3390/biom10030446.
Tumor suppressor genes in the locus (, , and ) function as biological barriers to transformation and are the most frequently silenced or deleted genes in human cancers. This gene silencing frequently occurs due to DNA methylation of the promoter regions, although the underlying mechanism is currently unknown. We present evidence that methylation of promoter is associated with DNA damage caused by interference between transcription and replication processes. Inhibition of replication or transcription significantly reduces the DNA damage and CpGs methylation of the promoter. We conclude that de novo methylation of the promoter regions is dependent on local DNA damage. DNA methylation reduces the expression of and ultimately removes this barrier to oncogene-induced senescence.
抑癌基因位于 ( 、 、 )位点,它们在细胞转化中充当生物学屏障,是人类癌症中最常发生沉默或缺失的基因。这种基因沉默通常是由于启动子区域的 DNA 甲基化引起的,但其潜在机制尚不清楚。我们提出的证据表明, 启动子的甲基化与转录和复制过程干扰引起的 DNA 损伤有关。复制或转录的抑制显著降低了 启动子的 DNA 损伤和 CpG 甲基化。我们的结论是,启动子区域的从头甲基化依赖于局部 DNA 损伤。DNA 甲基化降低了 的表达,最终消除了这种阻止癌基因诱导衰老的障碍。