The oncogene MYBL2 promotes the malignant phenotype and suppresses apoptosis through hedgehog signaling pathway in clear cell renal cell carcinoma

被引:4
|
作者
Yang, Wenjie [1 ]
Chen, Hualin [1 ]
Ma, Lin [1 ]
Wei, Mengchao [1 ]
Xue, Xiaoqiang [1 ]
Li, Yingjie [1 ]
Jin, Zhaoheng [1 ]
Dong, Jie [1 ]
Xiao, He [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Urol, Beijing 100000, Peoples R China
关键词
ccRCC; MYBL2; Proliferation; Apoptosis; SMO; CANCER; CHEMORESISTANCE; TRANSCRIPTION; RESISTANCE;
D O I
10.1016/j.heliyon.2024.e27772
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple cancers have been associated with MYB-related protein B (MYBL2), its involvement in clear cell renal cell carcinoma (ccRCC) has yet to be demonstrated. Our study revealed a significant upregulation of MYBL2 in ccRCC tissues, correlating with clinicopathological features and patient prognosis. Increased MYBL2 expression promoted cell proliferation and suppressed apoptosis. RNA-seq analysis unveiled a reduction in smoothened (SMO) expression upon MYBL2 silencing. However, luciferase and chromatin immunoprecipitation (ChIP) assays demonstrated MYBL2's positive regulation of SMO expression by directly targeting the SMO promoter. Reintroduction of SMO expression in MYBL2-knocked down cells partially restored cell proliferation and mitigated apoptosis inhibition. Overall, these results indicate that MYBL2 facilitates ccRCC progression by enhancing SMO expression, suggesting its potential as an intriguing drug target for ccRCC therapy.
引用
收藏
页数:14
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