Joint Laboratory for Translational Cancer Research of Chinese Medicine of the Ministry of Education of the People's Republic of China, International Institute for Translational Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, 510006, Guangdong, China.
School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
J Hematol Oncol. 2019 Dec 4;12(1):129. doi: 10.1186/s13045-019-0811-9.
Histone demethylase LSD1 plays key roles during carcinogenesis, targeting LSD1 is becoming an emerging option for the treatment of cancers. Numerous LSD1 inhibitors have been reported to date, some of them such as TCP, ORY-1001, GSK-2879552, IMG-7289, INCB059872, CC-90011, and ORY-2001 currently undergo clinical assessment for cancer therapy, particularly for small lung cancer cells (SCLC) and acute myeloid leukemia (AML). This review is to provide a comprehensive overview of LSD1 inhibitors in clinical trials including molecular mechanistic studies, clinical efficacy, adverse drug reactions, and PD/PK studies and offer prospects in this field.
组蛋白去甲基化酶 LSD1 在致癌过程中发挥着关键作用,靶向 LSD1 正成为癌症治疗的新兴选择。迄今为止,已经报道了许多 LSD1 抑制剂,其中一些如 TCP、ORY-1001、GSK-2879552、IMG-7289、INCB059872、CC-90011 和 ORY-2001,目前正在进行癌症治疗的临床评估,特别是针对小细胞肺癌 (SCLC) 和急性髓系白血病 (AML)。本综述旨在提供临床试验中 LSD1 抑制剂的全面概述,包括分子机制研究、临床疗效、药物不良反应以及 PD/PK 研究,并对该领域的前景进行展望。