Early Phase Trials and Sarcoma Units, Institut Bergonié, 229 cours de l'Argonne, 33000 Bordeaux, France.
Pharmacol Ther. 2016 Sep;165:26-31. doi: 10.1016/j.pharmthera.2016.05.003. Epub 2016 May 11.
Besides being a genetic disease, cancer is also an epigenetic disease. The histone methyltransferase EZH2 is the catalytic subunit of PRC2, a highly conserved protein complex that regulates gene expression by methylating lysine 27 on histone H3. Given its role in tumorigenesis and its prognostic value in several tumor types, this protein appears a relevant therapeutic target. This review focuses on the preclinical and preliminary clinical results of studies investigating EZH2 inhibitors in human malignancies. These emerging data suggest that EZH2 inhibitors represent a very promising class of drugs, which will probably have a major impact on improving outcome and reducing toxicity for patients with indolent and aggressive B-cell lymphomas and other specific solid tumors.
除了是一种遗传疾病外,癌症也是一种表观遗传疾病。组蛋白甲基转移酶 EZH2 是 PRC2 的催化亚基,PRC2 是一种高度保守的蛋白质复合物,通过在组蛋白 H3 上的赖氨酸 27 位甲基化来调节基因表达。鉴于其在肿瘤发生中的作用及其在几种肿瘤类型中的预后价值,该蛋白似乎是一个相关的治疗靶点。本综述重点介绍了研究 EZH2 抑制剂在人类恶性肿瘤中的临床前和初步临床研究结果。这些新出现的数据表明,EZH2 抑制剂代表了一类非常有前途的药物,它们可能会对改善惰性和侵袭性 B 细胞淋巴瘤以及其他特定实体瘤患者的预后和降低毒性产生重大影响。