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Positive feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis

Authors :
Zhang, Ming-xiao
Zhang, Li-zhen
Fu, Liang-min
Yao, Hao-hua
Tan, Lei
Feng, Zi-hao
Li, Jia-ying
Lu, Jun
Pan, Yi-hui
Shu, Guan-nan
Li, Peng-ju
Tang, Yi-ming
Liao, Zhuang-yao
Wei, Jin-huan
Chen, Wei
Guo, Jian-ping
Luo, Jun-hang
Chen, Zhen-hua
Source :
Oncogene; September 2021, Vol. 40 Issue: 37 p5639-5650, 12p
Publication Year :
2021

Abstract

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. VHLdeficiency-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.

Details

Language :
English
ISSN :
09509232 and 14765594
Volume :
40
Issue :
37
Database :
Supplemental Index
Journal :
Oncogene
Publication Type :
Periodical
Accession number :
ejs57259963
Full Text :
https://doi.org/10.1038/s41388-021-01971-7