Positive feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis
Autor: | Li-Zhen Zhang, Liang-Min Fu, Lei Tan, Yi-Hui Pan, Jinhuan Wei, Pengju Li, Wei Chen, Zhenhua Chen, Hao-Hua Yao, Junhang Luo, Guan-Nan Shu, Mingxiao Zhang, Jiaying Li, Jian-Ping Guo, Yiming Tang, Jun Lu, Zhuangyao Liao, Zihao Feng |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Cancer Research Carcinogenesis Biology medicine.disease_cause Article Metastasis Prognostic markers 03 medical and health sciences 0302 clinical medicine Downregulation and upregulation Genetics medicine Humans Enhancer Carcinoma Renal Cell Molecular Biology Mechanism (biology) Ubiquitination medicine.disease Renal cell carcinoma Kidney Neoplasms Up-Regulation PVT1 Clear cell renal cell carcinoma 030104 developmental biology 030220 oncology & carcinogenesis Cancer research RNA Long Noncoding Function (biology) |
Zdroj: | Oncogene |
ISSN: | 1476-5594 0950-9232 |
Popis: | Long noncoding RNAs (lncRNAs) have been reported to exert important roles in tumors, including clear cell renal cell carcinoma (ccRCC). PVT1 is an important oncogenic lncRNA which has critical effects on onset and development of various cancers, however, the underlying mechanism of PVT1 functioning in ccRCC remains largely unknown. VHL deficiency-induced HIF2α accumulation is one of the major factors for ccRCC. Here, we identified the potential molecular mechanism of PVT1 in promoting ccRCC development by stabilizing HIF2α. PVT1 was significantly upregulated in ccRCC tissues and high PVT1 expression was associated with poor prognosis of ccRCC patients. Both gain-of-function and loss-of function experiments revealed that PVT1 enhanced ccRCC cells proliferation, migration, and invasion and induced tumor angiogenesis in vitro and in vivo. Mechanistically, PVT1 interacted with HIF2α protein and enhanced its stability by protecting it from ubiquitination-dependent degradation, thereby exerting its biological significance. Meanwhile, HIF2α bound to the enhancer of PVT1 to transactivate its expression. Furthermore, HIF2α specific inhibitor could repress PVT1 expression and its oncogenic functions. Therefore, our study demonstrates that the PVT1/ HIF2α positive feedback loop involves in tumorigenesis and progression of ccRCC, which may be exploited for anticancer therapy. |
Databáze: | OpenAIRE |
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