Wang Cong, Li Hongyan, Wu Lei, Jiao Xueli, Jin Zihui, Zhu Yujie, Fang Ziling, Zhang Xiaodong, Huang Haishan, Zhao Lingling
Key Laboratory of Laboratory Medicine, Ministry of Education, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
Department of General Surgery, Heze Municipal Hospital, Heze, China.
Front Oncol. 2021 Apr 22;11:668743. doi: 10.3389/fonc.2021.668743. eCollection 2021.
Coiled-coil domain-containing 68 (CCDC68) plays different roles in cancer and is predicted as a tumor suppressor in human colorectal cancer (CRC). However, the specific role of CCDC68 in CRC and the underlying mechanisms remain unknown. Here, we showed that CCDC68 expression was lower in CRC than that in corresponding normal tissues, and CCDC68 level was positively correlated with disease-free survival. Ectopic expression of CCDC68 decreased CRC cell proliferation and suppressed the growth of CRC xenograft tumors . CCDC68 caused G0/G1 cell cycle arrest, downregulated CDK4, and upregulated ITCH, the E3 ubiquitin ligase responsible for CDK4 protein degradation. This increased CDK4 degradation, which decreased CDK4 protein levels and inhibited CRC tumor growth. Collectively, the present results identify a novel CDK4 regulatory axis consisting of CCDC68 and ITCH, which suggest that CCDC68 is a promising target for the treatment of CRC.
含卷曲螺旋结构域蛋白68(CCDC68)在癌症中发挥着不同作用,在人类结直肠癌(CRC)中被预测为肿瘤抑制因子。然而,CCDC68在CRC中的具体作用及潜在机制仍不清楚。在此,我们发现CRC中CCDC68的表达低于相应正常组织,且CCDC68水平与无病生存期呈正相关。CCDC68的异位表达降低了CRC细胞增殖,并抑制了CRC异种移植瘤的生长。CCDC68导致G0/G1期细胞周期停滞,下调CDK4,并上调ITCH,ITCH是负责CDK4蛋白降解的E3泛素连接酶。这增加了CDK4的降解,从而降低了CDK4蛋白水平并抑制了CRC肿瘤生长。总体而言,目前的结果确定了一个由CCDC68和ITCH组成的新型CDK4调节轴,这表明CCDC68是治疗CRC的一个有前景的靶点。