Positive feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis
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...
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Veröffentlicht in: | Oncogene 2021-09, Vol.40 (37), p.5639-5650 |
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creator | 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 |
description | 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. |
doi_str_mv | 10.1038/s41388-021-01971-7 |
format | Article |
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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.</description><identifier>ISSN: 0950-9232</identifier><identifier>ISSN: 1476-5594</identifier><identifier>EISSN: 1476-5594</identifier><identifier>DOI: 10.1038/s41388-021-01971-7</identifier><identifier>PMID: 34321604</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/51 ; 13/89 ; 14/32 ; 14/5 ; 38/77 ; 59/5 ; 631/67/322 ; 631/67/589/1588/1351 ; 64/60 ; 692/53/2422 ; 82/1 ; 82/29 ; 82/58 ; Angiogenesis ; Animals ; Apoptosis ; Basic Helix-Loop-Helix Transcription Factors - genetics ; Basic Helix-Loop-Helix Transcription Factors - metabolism ; Carcinogenesis - genetics ; Carcinoma, Renal Cell - genetics ; Carcinoma, Renal Cell - metabolism ; Carcinoma, Renal Cell - pathology ; Cell Biology ; Cell Line, Tumor ; Cell migration ; Cell Movement - genetics ; Cell proliferation ; Cell Proliferation - genetics ; Clear cell-type renal cell carcinoma ; Feedback ; Feedback, Physiological ; Female ; Gene Expression Regulation, Neoplastic ; Human Genetics ; Humans ; Internal Medicine ; Kidney cancer ; Kidney Neoplasms - genetics ; Kidney Neoplasms - metabolism ; Kidney Neoplasms - pathology ; Male ; Medicine ; Medicine & Public Health ; Metastases ; Mice ; Mice, Nude ; Neoplasm Metastasis ; Oncology ; Prognosis ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; Tumorigenesis ; Ubiquitination ; VHL protein</subject><ispartof>Oncogene, 2021-09, Vol.40 (37), p.5639-5650</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-727ff97e05db3bed8ec78b715026cb8b8bfb949b1d9ccfed857fa42250d9355f3</citedby><cites>FETCH-LOGICAL-c474t-727ff97e05db3bed8ec78b715026cb8b8bfb949b1d9ccfed857fa42250d9355f3</cites><orcidid>0000-0002-8889-5122 ; 0000-0002-5706-0990 ; 0000-0002-8158-0101</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41388-021-01971-7$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41388-021-01971-7$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34321604$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Ming-xiao</creatorcontrib><creatorcontrib>Zhang, Li-zhen</creatorcontrib><creatorcontrib>Fu, Liang-min</creatorcontrib><creatorcontrib>Yao, Hao-hua</creatorcontrib><creatorcontrib>Tan, Lei</creatorcontrib><creatorcontrib>Feng, Zi-hao</creatorcontrib><creatorcontrib>Li, Jia-ying</creatorcontrib><creatorcontrib>Lu, Jun</creatorcontrib><creatorcontrib>Pan, Yi-hui</creatorcontrib><creatorcontrib>Shu, Guan-nan</creatorcontrib><creatorcontrib>Li, Peng-ju</creatorcontrib><creatorcontrib>Tang, Yi-ming</creatorcontrib><creatorcontrib>Liao, Zhuang-yao</creatorcontrib><creatorcontrib>Wei, Jin-huan</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Guo, Jian-ping</creatorcontrib><creatorcontrib>Luo, Jun-hang</creatorcontrib><creatorcontrib>Chen, Zhen-hua</creatorcontrib><title>Positive feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis</title><title>Oncogene</title><addtitle>Oncogene</addtitle><addtitle>Oncogene</addtitle><description>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.</description><subject>13/51</subject><subject>13/89</subject><subject>14/32</subject><subject>14/5</subject><subject>38/77</subject><subject>59/5</subject><subject>631/67/322</subject><subject>631/67/589/1588/1351</subject><subject>64/60</subject><subject>692/53/2422</subject><subject>82/1</subject><subject>82/29</subject><subject>82/58</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Basic Helix-Loop-Helix Transcription Factors - genetics</subject><subject>Basic Helix-Loop-Helix Transcription Factors - metabolism</subject><subject>Carcinogenesis - genetics</subject><subject>Carcinoma, Renal Cell - genetics</subject><subject>Carcinoma, Renal Cell - metabolism</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Cell Biology</subject><subject>Cell Line, Tumor</subject><subject>Cell migration</subject><subject>Cell Movement - genetics</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - genetics</subject><subject>Clear cell-type renal cell carcinoma</subject><subject>Feedback</subject><subject>Feedback, Physiological</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Kidney cancer</subject><subject>Kidney Neoplasms - genetics</subject><subject>Kidney Neoplasms - metabolism</subject><subject>Kidney Neoplasms - pathology</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Neoplasm Metastasis</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>RNA, Long Noncoding - 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feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis</title><author>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, 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Biology</topic><topic>Cell Line, Tumor</topic><topic>Cell migration</topic><topic>Cell Movement - genetics</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - genetics</topic><topic>Clear cell-type renal cell carcinoma</topic><topic>Feedback</topic><topic>Feedback, Physiological</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Kidney cancer</topic><topic>Kidney Neoplasms - genetics</topic><topic>Kidney Neoplasms - metabolism</topic><topic>Kidney Neoplasms - pathology</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Neoplasm Metastasis</topic><topic>Oncology</topic><topic>Prognosis</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - 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titles)</collection><jtitle>Oncogene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Ming-xiao</au><au>Zhang, Li-zhen</au><au>Fu, Liang-min</au><au>Yao, Hao-hua</au><au>Tan, Lei</au><au>Feng, Zi-hao</au><au>Li, Jia-ying</au><au>Lu, Jun</au><au>Pan, Yi-hui</au><au>Shu, Guan-nan</au><au>Li, Peng-ju</au><au>Tang, Yi-ming</au><au>Liao, Zhuang-yao</au><au>Wei, Jin-huan</au><au>Chen, Wei</au><au>Guo, Jian-ping</au><au>Luo, Jun-hang</au><au>Chen, Zhen-hua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positive feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis</atitle><jtitle>Oncogene</jtitle><stitle>Oncogene</stitle><addtitle>Oncogene</addtitle><date>2021-09-16</date><risdate>2021</risdate><volume>40</volume><issue>37</issue><spage>5639</spage><epage>5650</epage><pages>5639-5650</pages><issn>0950-9232</issn><issn>1476-5594</issn><eissn>1476-5594</eissn><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.
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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>34321604</pmid><doi>10.1038/s41388-021-01971-7</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-8889-5122</orcidid><orcidid>https://orcid.org/0000-0002-5706-0990</orcidid><orcidid>https://orcid.org/0000-0002-8158-0101</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8445819 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | 13/51 13/89 14/32 14/5 38/77 59/5 631/67/322 631/67/589/1588/1351 64/60 692/53/2422 82/1 82/29 82/58 Angiogenesis Animals Apoptosis Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism Carcinogenesis - genetics Carcinoma, Renal Cell - genetics Carcinoma, Renal Cell - metabolism Carcinoma, Renal Cell - pathology Cell Biology Cell Line, Tumor Cell migration Cell Movement - genetics Cell proliferation Cell Proliferation - genetics Clear cell-type renal cell carcinoma Feedback Feedback, Physiological Female Gene Expression Regulation, Neoplastic Human Genetics Humans Internal Medicine Kidney cancer Kidney Neoplasms - genetics Kidney Neoplasms - metabolism Kidney Neoplasms - pathology Male Medicine Medicine & Public Health Metastases Mice Mice, Nude Neoplasm Metastasis Oncology Prognosis RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism Tumorigenesis Ubiquitination VHL protein |
title | Positive feedback regulation of lncRNA PVT1 and HIF2α contributes to clear cell renal cell carcinoma tumorigenesis and metastasis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T06%3A08%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Positive%20feedback%20regulation%20of%20lncRNA%20PVT1%20and%20HIF2%CE%B1%20contributes%20to%20clear%20cell%20renal%20cell%20carcinoma%20tumorigenesis%20and%20metastasis&rft.jtitle=Oncogene&rft.au=Zhang,%20Ming-xiao&rft.date=2021-09-16&rft.volume=40&rft.issue=37&rft.spage=5639&rft.epage=5650&rft.pages=5639-5650&rft.issn=0950-9232&rft.eissn=1476-5594&rft_id=info:doi/10.1038/s41388-021-01971-7&rft_dat=%3Cproquest_pubme%3E2573126166%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2573126166&rft_id=info:pmid/34321604&rfr_iscdi=true |