Circ-IP6K2 suppresses tumor progression by modulating the miR-1292-5p/CAMK2N1 signal in clear cell renal cell carcinoma
作者全名:"Tang, Jian-ying; Yang, Lu; Wu, Qing-Jian; Yang, Ying; Su, Yuan-Yuan; Chen, Yi-Rong; Mu, Jiao"
作者地址:"[Tang, Jian-ying; Yang, Lu; Yang, Ying; Su, Yuan-Yuan; Chen, Yi-Rong; Mu, Jiao] Chongqing Med Univ, Univ Town Hosp, Dept Nephrol, 55 Rd Univ Town, Chongqing 401331, Peoples R China; [Wu, Qing-Jian] Third Mil Med Univ, Xinqiao Hosp, Dept Urol, Chongqing 400037, Peoples R China"
通信作者:"Mu, J (通讯作者),Chongqing Med Univ, Univ Town Hosp, Dept Nephrol, 55 Rd Univ Town, Chongqing 401331, Peoples R China."
来源:FUNCTIONAL & INTEGRATIVE GENOMICS
ESI学科分类:MOLECULAR BIOLOGY & GENETICS
WOS号:WOS:001268205700001
JCR分区:Q2
影响因子:2.9
年份:2024
卷号:24
期号:4
开始页:
结束页:
文献类型:Article
关键词:miR-1292-5p; Progression; Clear cell renal cell carcinoma
摘要:"Renal cell carcinoma (RCC) is a malignant tumor originating from the epithelial cells of the renal tubules. The clear cell RCC subtype is closely linked to a poor prognosis due to its rapid progression. Circular RNA (circRNA) is a novel class of regulatory RNA molecules that play a role in the development of ccRCC, although their functions have not been fully elucidated. In this study, we identified a significant downregulation of circ-IP6K2 in ccRCC tissues based on data from the GSE100186 dataset. The decreased expression of circ-IP6K2 correlated with the progression of TNM stage and histological grade, and was also associated with decreased overall survival rates in ccRCC patients. Moreover, our findings revealed that circ-IP6K2 expression suppressed proliferation, migration, and invasion capabilities in vitro, and inhibited xenograft growth in vivo. Mechanistically, circ-IP6K2 acted as a sponge for miR-1292-5p in ccRCC cells, which in turn targeted the 3'UTR of CAMK2N1, leading to a decrease in its expression. CAMK2N1 was identified as a tumor suppressor that negatively regulated the beta-catenin/c-Myc oncogenic signaling pathway. Additionally, we confirmed a positive correlation between the expression of circ-IP6K2 and CAMK2N1 in ccRCC. Circ-IP6K2 functions to impede the progression of ccRCC by modulating the miR-1292-5p/CAMK2N1 axis. These findings shed new light on the molecular mechanisms driving ccRCC progression and suggest potential therapeutic targets for the treatment of ccRCC."
基金机构:"Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission"
基金资助正文:No Statement Available