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The HBV Specially-Related Long Noncoding RNA HBV-SRL Involved in the Pathogenesis of Hepatocellular Carcinoma
Hepatitis B virus (HBV) is one of the major risk factors for HCC (hepatocellular carcinoma) occurrence with a diverse role in the pathogenesis of HCC. More works need to be performed to elucidate a more thorough understanding of the molecular mechanisms involving in HBV-induced HCC, although some me...
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Published in: | Journal of oncology 2022-07, Vol.2022, p.9034105-11 |
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description | Hepatitis B virus (HBV) is one of the major risk factors for HCC (hepatocellular carcinoma) occurrence with a diverse role in the pathogenesis of HCC. More works need to be performed to elucidate a more thorough understanding of the molecular mechanisms involving in HBV-induced HCC, although some mechanisms such as genome integration have been reported. In the present study, aberrantly expressed lncRNAs were identified between HCC tumor tissues with or without HBV infection. Among these molecules, HBV specially-related long noncoding RNA (HBV-SRL) was further found to correlate with poor prognosis and a shorter overall survival time in HCC patients with HBV infection. Additionally, HBV-SRL was found function as oncogene by upregulating the NF-κB2 expression. These data suggest that HBV infection altered gene expression pattern in liver cells which contributed to HBV-related HCC development, and HBV-SRL may serve as a new molecular marker or potential therapeutic target of HBV-related HCC. |
doi_str_mv | 10.1155/2022/9034105 |
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More works need to be performed to elucidate a more thorough understanding of the molecular mechanisms involving in HBV-induced HCC, although some mechanisms such as genome integration have been reported. In the present study, aberrantly expressed lncRNAs were identified between HCC tumor tissues with or without HBV infection. Among these molecules, HBV specially-related long noncoding RNA (HBV-SRL) was further found to correlate with poor prognosis and a shorter overall survival time in HCC patients with HBV infection. Additionally, HBV-SRL was found function as oncogene by upregulating the NF-κB2 expression. These data suggest that HBV infection altered gene expression pattern in liver cells which contributed to HBV-related HCC development, and HBV-SRL may serve as a new molecular marker or potential therapeutic target of HBV-related HCC.</description><identifier>ISSN: 1687-8450</identifier><identifier>EISSN: 1687-8450</identifier><identifier>DOI: 10.1155/2022/9034105</identifier><identifier>PMID: 35847364</identifier><language>eng</language><publisher>Egypt: Hindawi</publisher><subject>Antisense RNA ; DNA methylation ; Drug resistance ; Gene expression ; Genomes ; Genomics ; Health aspects ; Hepatitis B ; Hepatoma ; Infection ; Infections ; Liver cancer ; Medical prognosis ; Metastasis ; Pathogenesis ; Prognosis ; Proteins ; Roles ; Tumors ; Viral infections</subject><ispartof>Journal of oncology, 2022-07, Vol.2022, p.9034105-11</ispartof><rights>Copyright © 2022 Cunzhen Zhang et al.</rights><rights>COPYRIGHT 2022 John Wiley & Sons, Inc.</rights><rights>Copyright © 2022 Cunzhen Zhang et al. This work is licensed 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><rights>Copyright © 2022 Cunzhen Zhang et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c433t-2e010d65162cbd8fbdf3d708a159e60ea0d7bd48c8617a13d47830e324d031543</cites><orcidid>0000-0003-3273-0115 ; 0000-0002-8476-5451 ; 0000-0002-9276-7086 ; 0000-0002-5607-4143 ; 0000-0003-1874-3630 ; 0000-0001-7933-7850 ; 0000-0002-0511-8417 ; 0000-0001-5633-1958 ; 0000-0001-6547-0650 ; 0000-0003-0886-149X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2690837777/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2690837777?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35847364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Mei, Jie</contributor><contributor>Jie Mei</contributor><creatorcontrib>Zhang, Cunzhen</creatorcontrib><creatorcontrib>Lu, Lei</creatorcontrib><creatorcontrib>Xin, Haibei</creatorcontrib><creatorcontrib>Zhang, Minfeng</creatorcontrib><creatorcontrib>Ding, Zhiwen</creatorcontrib><creatorcontrib>Li, Qiaomei</creatorcontrib><creatorcontrib>Chen, Kuang</creatorcontrib><creatorcontrib>Hu, Minggen</creatorcontrib><creatorcontrib>Liu, Shupeng</creatorcontrib><creatorcontrib>Li, Nan</creatorcontrib><title>The HBV Specially-Related Long Noncoding RNA HBV-SRL Involved in the Pathogenesis of Hepatocellular Carcinoma</title><title>Journal of oncology</title><addtitle>J Oncol</addtitle><description>Hepatitis B virus (HBV) is one of the major risk factors for HCC (hepatocellular carcinoma) occurrence with a diverse role in the pathogenesis of HCC. More works need to be performed to elucidate a more thorough understanding of the molecular mechanisms involving in HBV-induced HCC, although some mechanisms such as genome integration have been reported. In the present study, aberrantly expressed lncRNAs were identified between HCC tumor tissues with or without HBV infection. Among these molecules, HBV specially-related long noncoding RNA (HBV-SRL) was further found to correlate with poor prognosis and a shorter overall survival time in HCC patients with HBV infection. Additionally, HBV-SRL was found function as oncogene by upregulating the NF-κB2 expression. 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More works need to be performed to elucidate a more thorough understanding of the molecular mechanisms involving in HBV-induced HCC, although some mechanisms such as genome integration have been reported. In the present study, aberrantly expressed lncRNAs were identified between HCC tumor tissues with or without HBV infection. Among these molecules, HBV specially-related long noncoding RNA (HBV-SRL) was further found to correlate with poor prognosis and a shorter overall survival time in HCC patients with HBV infection. Additionally, HBV-SRL was found function as oncogene by upregulating the NF-κB2 expression. 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subjects | Antisense RNA DNA methylation Drug resistance Gene expression Genomes Genomics Health aspects Hepatitis B Hepatoma Infection Infections Liver cancer Medical prognosis Metastasis Pathogenesis Prognosis Proteins Roles Tumors Viral infections |
title | The HBV Specially-Related Long Noncoding RNA HBV-SRL Involved in the Pathogenesis of Hepatocellular Carcinoma |
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