蛋白激酶B
下调和上调
多发性骨髓瘤
癌变
癌症研究
基因敲除
细胞凋亡
肿瘤进展
细胞生长
体内
细胞周期进展
细胞周期
细胞
PI3K/AKT/mTOR通路
化学
生物
细胞生物学
信号转导
免疫学
癌症
生物化学
基因
遗传学
作者
Haiming Kou,Shuqin Jiang,Xueqiong Wu,Changhua Jing,Xinxin Xu,Jiaju Wang,Cui Zhang,Wenting Liu,Y Gao,Quancang Men,Ping Lu,Zhenhui Lv
摘要
Abstract Multiple myeloma (MM) is an incurable hematological malignancy, and the number of MM patients is increasing year by year. Zinc finger protein 655 (ZNF655) has been shown to regulate various biological processes and is implicated in the progression of many diseases. However, the roles of ZNF655 in MM progression remains unclear. In this study, we aimed to explore the effects of ZNF655 on progression by detecting the alteration of the phenotypes and tumorigenesis induced by ZNF655 knockdown in MM. The expression level of ZNF655 in MM was clarified by real‐time quantitative polymerase chain reaction assays. Furthermore, loss‐of‐function assays in vitro and in vivo was investigated the biological functions of ZNF655 in MM. These findings revealed that ZNF655 depletion remarkably inhibited MM cell proliferation, arrested cell cycle, and induced cell apoptosis. Mechanistically, ZNF655 was found to regulate AKT in MM. In conclusion, this study indicated that ZNF655 regulated the progression of MM via AKT activation and downregulation of ZNF655 may be a promising antitumor strategy in MM.
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