Xu Xin, Li Shaoyan, Cui Ximao, Han Kunkun, Wang Jun, Hou Xiaodan, Cui Long, He Songbing, Xiao Jiecheng, Yang Yili
Center for Systems Medicine, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences, Suzhou, China.
School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Front Oncol. 2019 Dec 18;9:1406. doi: 10.3389/fonc.2019.01406. eCollection 2019.
Mutations and altered expression of deubiquitinating enzymes (DUBs) have been found associated with many human diseases including cancers. In this study, Ubiquitin specific protease 1 (USP1) expression was found significantly increased in some colorectal cancers (CRC). The elevated USP1 level was associated with short overall survival of patients and with advanced stages of cancers. In cultured CRC cells, knockdown of USP1 induced growth arrest at G/M of cell cycle and reduced the expression of anti-apoptotic proteins Bcl-2 and Mcl-1. Its knockdown also led to reduction of DNA-repair related substrates FANCD2 and ID1. Further investigations found that small molecular inhibitor of USP1 ML323 sensitized CRC cells to DNA-targeting chemotherapeutics, including doxorubicin, TOPI/II inhibitors, and PARP inhibitor, but not to 5-Fu. These results indicate that USP1 plays a critical in colorectal cancer cell survival and is a promising target for anti-colorectal cancer chemotherapy. Targeting USP1 may represent an effective strategy to regulate the DNA-repairing system.
去泛素化酶(DUBs)的突变和表达改变已被发现与包括癌症在内的许多人类疾病相关。在本研究中,发现泛素特异性蛋白酶1(USP1)在一些结直肠癌(CRC)中表达显著增加。USP1水平升高与患者总生存期短以及癌症晚期相关。在培养的CRC细胞中,敲低USP1可诱导细胞周期在G/M期生长停滞,并降低抗凋亡蛋白Bcl-2和Mcl-1的表达。其敲低还导致DNA修复相关底物FANCD2和ID1减少。进一步研究发现,USP1的小分子抑制剂ML323使CRC细胞对靶向DNA的化疗药物敏感,包括阿霉素、TOPI/II抑制剂和PARP抑制剂,但对5-氟尿嘧啶不敏感。这些结果表明,USP1在结直肠癌细胞存活中起关键作用,是抗结直肠癌化疗的一个有前景的靶点。靶向USP1可能是调节DNA修复系统的有效策略。