Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117597, Singapore.
National University Health System (NUHS), Singapore, 119228, Singapore.
Cell Mol Life Sci. 2018 Sep;75(18):3381-3392. doi: 10.1007/s00018-018-2866-0. Epub 2018 Jul 12.
Technological breakthroughs in genomics have had a significant impact on clinical therapy for human diseases, allowing us to use patient genetic differences to guide medical care. The "synthetic lethal approach" leverages on cancer-specific genetic rewiring to deliver a therapeutic regimen that preferentially targets malignant cells while sparing normal cells. The utility of this system is evident in several recent studies, particularly in poor prognosis cancers with loss-of-function mutations that become "treatable" when two otherwise discrete and unrelated genes are targeted simultaneously. This review focuses on the chemotherapeutic targeting of epigenetic alterations in cancer cells and consolidates a network that outlines the interplay between epigenetic and genetic regulators in DNA damage repair. This network consists of numerous synergistically acting relationships that are druggable, even in recalcitrant triple-negative breast cancer. This collective knowledge points to the dawn of a new era of personalized medicine.
基因组学的技术突破对人类疾病的临床治疗产生了重大影响,使我们能够利用患者的基因差异来指导医疗护理。“合成致死方法”利用肿瘤特异性基因重排,提供一种治疗方案,优先靶向恶性细胞,同时保护正常细胞。该系统在几项最近的研究中得到了证实,特别是在预后不良的癌症中,当同时靶向两个原本离散且不相关的基因时,具有功能丧失突变的癌症变得“可治疗”。本综述重点介绍了癌细胞中表观遗传改变的化疗靶向,并整合了一个网络,概述了表观遗传和遗传调节剂在 DNA 损伤修复中的相互作用。该网络由许多协同作用的关系组成,即使在难治性三阴性乳腺癌中也是可用药的。这些集体知识表明个性化医疗的新时代即将到来。