Sarthy Jay F, Henikoff Steven, Ahmad Kami
Howard Hughes Medical Institute, Chevy Chase, MD, USA; Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA.
Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA.
Trends Cancer. 2019 Mar;5(3):183-194. doi: 10.1016/j.trecan.2019.01.003. Epub 2019 Feb 26.
Cancer accounts for ∼9 million deaths per year worldwide, predominantly affecting adults. Adult malignancies are usually examined after extensive clonal evolution and carry many mutations, obscuring the individual contributions of these alterations to oncogenesis. By contrast, pediatric cancers often contain few mutations, many of which cause defects in chromatin-associated proteins. We explore here the roles that chromatin plays in oncogenesis. We highlight how the developmental regulation of cell proliferation genes and the degradation of chromosome ends are two major bottlenecks in the evolution of malignant cells, and point to a third bottleneck where epigenomic dysfunction triggers expression of tumor-suppressor genes, limiting the development of aggressive and metastatic features in tumors. We also identify opportunities for chromatin-based therapies.
癌症每年在全球导致约900万人死亡,主要影响成年人。成人恶性肿瘤通常在经历广泛的克隆进化后才被检查,并且携带许多突变,这使得这些改变对肿瘤发生的个体贡献变得模糊不清。相比之下,儿童癌症通常含有较少的突变,其中许多突变会导致染色质相关蛋白出现缺陷。我们在此探讨染色质在肿瘤发生中所起的作用。我们强调细胞增殖基因的发育调控和染色体末端的降解是恶性细胞进化中的两个主要瓶颈,并指出第三个瓶颈,即表观基因组功能障碍触发肿瘤抑制基因的表达,限制肿瘤侵袭性和转移性特征的发展。我们还确定了基于染色质的治疗机会。