Genitourinary Program and Department of Cancer Pathology and Prevention, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Cancer J. 2013 Jul-Aug;19(4):333-40. doi: 10.1097/PPO.0b013e3182a09e07.
Recent investigations of renal cell carcinoma (RCC) have revealed several epigenetic modifications, as well as alterations in the genes and enzymes that regulate these changes. Preclinical models have revealed that histone gene modifiers and epigenetic alterations may play a critical role in RCC tumorigenesis. Specific changes in DNA methylation and mutations of histone modifiers have been identified and may be associated with an aggressive phenotype. In addition, the potential of reversing the effects of these enzymes and hence reversing the cellular epigenetic landscape to a "normal phenotype" have led to an increasing interest in developing targeted chromatin remodeling agents. However, the translation of the understanding of these changes to the clinic for the treatment of RCC has posed significant challenges, partly due to tumor heterogeneity. This review describes the aberrant histone and DNA alterations recently reported in RCC and highlights the potential targeted chromatin remodeling therapies in the management of this disease.
最近对肾细胞癌 (RCC) 的研究揭示了几种表观遗传修饰,以及调节这些变化的基因和酶的改变。临床前模型表明,组蛋白基因修饰剂和表观遗传改变可能在 RCC 肿瘤发生中起关键作用。已经确定了特定的 DNA 甲基化变化和组蛋白修饰剂的突变,并且可能与侵袭性表型相关。此外,逆转这些酶的作用,从而将细胞表观遗传景观逆转到“正常表型”的潜力,导致人们越来越有兴趣开发靶向染色质重塑剂。然而,将这些变化的理解从临床转化为治疗 RCC 提出了重大挑战,部分原因是肿瘤异质性。本文描述了最近在 RCC 中报道的异常组蛋白和 DNA 改变,并强调了在这种疾病管理中潜在的靶向染色质重塑治疗方法。