دورية أكاديمية

CircCSNK1G3 up-regulates miR-181b to promote growth and metastasis via TIMP3-mediated epithelial to mesenchymal transitions in renal cell carcinoma.

التفاصيل البيبلوغرافية
العنوان: CircCSNK1G3 up-regulates miR-181b to promote growth and metastasis via TIMP3-mediated epithelial to mesenchymal transitions in renal cell carcinoma.
المؤلفون: Wen Li, Yang-Yi-Yan Song, Ting Rao, Wei-Min Yu, Yuan Ruan, Jin-Zhuo Ning, Xiao-Bing Yao, Song-Yi-Sha Yang, Fan Cheng
المصدر: Journal of Cellular & Molecular Medicine; Mar2022, Vol. 26 Issue 6, p1729-1741, 13p
مصطلحات موضوعية: EPITHELIAL-mesenchymal transition, RENAL cell carcinoma, RENAL cancer, CANCER relapse, METASTASIS
مستخلص: Renal cell carcinoma (RCC) is the most common form of kidney cancer, with a high recurrence rate and metastasis capacity. Circular RNAs (circRNAs) have been suggested to act as the critical regulator in several diseases. This study is designed to investigate the role of circCSNK1G3 on RCC progression. We observed a highly expression of circCSNK1G3 in RCC tissues compared with normal tissues. The aberrantly circCSNK1G3 promoted the tumour growth and metastasis in RCC. In the subsequent mechanism investigation, we discovered that the tumour-promoting effects of circCSNK1G3 were, at least partly, achieved by up-regulating miR-181b. Increased miR-181b inhibits several tumour suppressor gene, including CYLD, LATS2, NDRG2 and TIMP3. Furthermore, the decreased TIMP3 leads to the enhanced epithelial to mesenchymal transition (EMT) process, thus promoting the cancer metastasis. In conclusion, we identified the oncogenic role of circCSNK1G3 in RCC progression and demonstrated the regulatory role of circCSNK1G3 induced miR-181b expression, which leads to TIMP3-mediated EMT process, thus resulting in tumour growth and metastasis in RCC. This study reveals the promise of circCSNK1G3 to be developed as a potential diagnostic and prognostic biomarker in the clinic. And the roles of circ-CSNK1G3 in cancer research deserve further investigation. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:15821838
DOI:10.1111/jcmm.15911