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The potential of CircRNA1002 as a biomarker in hepatitis B virus-related hepatocellular carcinoma
Although hepatocellular carcinoma (HCC) is the most common type of primary liver cancer, there is a lack of effective diagnostic measures. Circular RNAs (circRNAs) can be used as biomarkers for monitoring the occurrence and development of HCC. However, a convenient and reliable serum circRNA biomark...
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Published in: | PeerJ (San Francisco, CA) CA), 2022-06, Vol.10, p.e13640-e13640, Article e13640 |
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description | Although hepatocellular carcinoma (HCC) is the most common type of primary liver cancer, there is a lack of effective diagnostic measures. Circular RNAs (circRNAs) can be used as biomarkers for monitoring the occurrence and development of HCC. However, a convenient and reliable serum circRNA biomarker is not currently available.
CircRNA expression profiles were explored using high-throughput sequencing technology, and targeted circRNAs and mRNAs were validated by quantitative reverse transcription PCR (RT-qPCR). The biological functions of circRNAs were investigated using Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Downstream miRNAs and mRNAs of dysregulated circRNAs were predicted using TargetScan, miRanda, and miRDB; then circRNA-miRNA-mRNA interaction networks were constructed based on sequencing data and the Cancer Genome Atlas (TCGA).
A total of 50,327 circRNAs were identified, with 1,187 circRNAs significantly differentially expressed between hepatitis B virus (HBV)-related HCC and HBV asymptomatic carriers. Among these circRNAs, four (circRNA1002, circRNA7941, circRNA 39338, and circRNA44142) were validated by RT-qPCR as being statistically different either in HCC tissue or serum samples. circRNA1002 was significantly down-regulated in both HCC serum and tissue, indicating its reliability. Bioinformatics analysis showed that circRNA1002-associated genes were enriched in GO terms relating to hormone pathway and cell-cell interaction processes, which are involved in the progression of HCC.
Our circRNA analysis of HCC patients and HBV asymptomatic carriers showed that circRNA1002 may be a reliable serum biomarker for HCC. These results could provide an improved assay for the early detection of HCC. |
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CircRNA expression profiles were explored using high-throughput sequencing technology, and targeted circRNAs and mRNAs were validated by quantitative reverse transcription PCR (RT-qPCR). The biological functions of circRNAs were investigated using Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Downstream miRNAs and mRNAs of dysregulated circRNAs were predicted using TargetScan, miRanda, and miRDB; then circRNA-miRNA-mRNA interaction networks were constructed based on sequencing data and the Cancer Genome Atlas (TCGA).
A total of 50,327 circRNAs were identified, with 1,187 circRNAs significantly differentially expressed between hepatitis B virus (HBV)-related HCC and HBV asymptomatic carriers. Among these circRNAs, four (circRNA1002, circRNA7941, circRNA 39338, and circRNA44142) were validated by RT-qPCR as being statistically different either in HCC tissue or serum samples. circRNA1002 was significantly down-regulated in both HCC serum and tissue, indicating its reliability. Bioinformatics analysis showed that circRNA1002-associated genes were enriched in GO terms relating to hormone pathway and cell-cell interaction processes, which are involved in the progression of HCC.
Our circRNA analysis of HCC patients and HBV asymptomatic carriers showed that circRNA1002 may be a reliable serum biomarker for HCC. These results could provide an improved assay for the early detection of HCC.</description><identifier>ISSN: 2167-8359</identifier><identifier>EISSN: 2167-8359</identifier><identifier>DOI: 10.7717/peerj.13640</identifier><identifier>PMID: 35782101</identifier><language>eng</language><publisher>United States: PeerJ. Ltd</publisher><subject>Asymptomatic ; Bioinformatics ; Biomarkers ; Biomarkers - metabolism ; Biopsy ; Cancer therapies ; Carcinoma, Hepatocellular - diagnosis ; Circular RNA ; Gastroenterology and Hepatology ; Gene Expression Profiling - methods ; Genomes ; Genomics ; Hepatitis B ; Hepatitis B virus ; Hepatitis B virus - genetics ; Hepatocellular carcinoma ; Hepatoma ; Humans ; Liver ; Liver cancer ; Liver Neoplasms - diagnosis ; Medical Genetics ; Medical prognosis ; Medical research ; Metastasis ; MicroRNA ; MicroRNAs - genetics ; miRNA ; Molecular Biology ; mRNA ; Next-generation sequencing ; Public Health ; Reproducibility of Results ; Reverse transcription ; RNA, Circular - genetics ; RNA, Messenger - genetics ; Serum biomarker</subject><ispartof>PeerJ (San Francisco, CA), 2022-06, Vol.10, p.e13640-e13640, Article e13640</ispartof><rights>2022 Li et al.</rights><rights>COPYRIGHT 2022 PeerJ. Ltd.</rights><rights>2022 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Li et al. 2022 Li et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-87ee1119bf36c5568e3cd743dc74108cfe203720ad98d355d0935fb4302b24b23</citedby><cites>FETCH-LOGICAL-c573t-87ee1119bf36c5568e3cd743dc74108cfe203720ad98d355d0935fb4302b24b23</cites><orcidid>0000-0001-7550-1254</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2681634162/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2681634162?pq-origsite=primo$$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/35782101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ying</creatorcontrib><creatorcontrib>Li, Ronghua</creatorcontrib><creatorcontrib>Cheng, Da</creatorcontrib><creatorcontrib>Fu, Xiaoyu</creatorcontrib><creatorcontrib>Fu, Lei</creatorcontrib><creatorcontrib>Peng, Shifang</creatorcontrib><title>The potential of CircRNA1002 as a biomarker in hepatitis B virus-related hepatocellular carcinoma</title><title>PeerJ (San Francisco, CA)</title><addtitle>PeerJ</addtitle><description>Although hepatocellular carcinoma (HCC) is the most common type of primary liver cancer, there is a lack of effective diagnostic measures. Circular RNAs (circRNAs) can be used as biomarkers for monitoring the occurrence and development of HCC. However, a convenient and reliable serum circRNA biomarker is not currently available.
CircRNA expression profiles were explored using high-throughput sequencing technology, and targeted circRNAs and mRNAs were validated by quantitative reverse transcription PCR (RT-qPCR). The biological functions of circRNAs were investigated using Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Downstream miRNAs and mRNAs of dysregulated circRNAs were predicted using TargetScan, miRanda, and miRDB; then circRNA-miRNA-mRNA interaction networks were constructed based on sequencing data and the Cancer Genome Atlas (TCGA).
A total of 50,327 circRNAs were identified, with 1,187 circRNAs significantly differentially expressed between hepatitis B virus (HBV)-related HCC and HBV asymptomatic carriers. Among these circRNAs, four (circRNA1002, circRNA7941, circRNA 39338, and circRNA44142) were validated by RT-qPCR as being statistically different either in HCC tissue or serum samples. circRNA1002 was significantly down-regulated in both HCC serum and tissue, indicating its reliability. Bioinformatics analysis showed that circRNA1002-associated genes were enriched in GO terms relating to hormone pathway and cell-cell interaction processes, which are involved in the progression of HCC.
Our circRNA analysis of HCC patients and HBV asymptomatic carriers showed that circRNA1002 may be a reliable serum biomarker for HCC. These results could provide an improved assay for the early detection of HCC.</description><subject>Asymptomatic</subject><subject>Bioinformatics</subject><subject>Biomarkers</subject><subject>Biomarkers - metabolism</subject><subject>Biopsy</subject><subject>Cancer therapies</subject><subject>Carcinoma, Hepatocellular - diagnosis</subject><subject>Circular RNA</subject><subject>Gastroenterology and Hepatology</subject><subject>Gene Expression Profiling - methods</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Hepatitis B</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatocellular carcinoma</subject><subject>Hepatoma</subject><subject>Humans</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Medical Genetics</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Metastasis</subject><subject>MicroRNA</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>Molecular Biology</subject><subject>mRNA</subject><subject>Next-generation sequencing</subject><subject>Public Health</subject><subject>Reproducibility of Results</subject><subject>Reverse transcription</subject><subject>RNA, Circular - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>Serum biomarker</subject><issn>2167-8359</issn><issn>2167-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt9rFDEQxxdRbKl98l0Cgghlz_zaJPsiXA-rhaIg9Tlks5PbnHubM9kt-N-bvavlTkweEiaf-c7kyxTFa4IXUhL5YQcQNwvCBMfPinNKhCwVq-rnR_ez4jKlDc5LUYEVe1mcsUoqSjA5L8x9B2gXRhhGb3oUHFr5aL9_XRKMKTIJGdT4sDXxJ0TkB9TBzox-9Aldowcfp1RG6M0I7eElWOj7qTcRWROtH3Lmq-KFM32Cy8fzovhx8-l-9aW8-_b5drW8K20l2VgqCUAIqRvHhK0qoYDZVnLWWskJVtYBxUxSbNpatayqWlyzyjWcYdpQ3lB2UdwedNtgNnoXfW76tw7G630gxLU2cfS2B40prpXIpVpKuHKyoc4QSZXgrpKSyqz18aC1m5ottDa7E01_Inr6MvhOr8ODrilXUs0C7x8FYvg1QRr11qfZGzNAmJKmQlU4_4LPfb_9B92EKQ7ZqpkignEijqi1yR_wgwu5rp1F9VJixUVNGc7U4j9U3i1svQ0DOJ_jJwnvjhI6MP3YpdBPow9DOgWvDqCNIaUI7skMgvU8iXo_iXo_iZl-c-zfE_t37tgfmfXVhQ</recordid><startdate>20220628</startdate><enddate>20220628</enddate><creator>Li, Ying</creator><creator>Li, Ronghua</creator><creator>Cheng, Da</creator><creator>Fu, Xiaoyu</creator><creator>Fu, Lei</creator><creator>Peng, Shifang</creator><general>PeerJ. 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Cheng, Da ; Fu, Xiaoyu ; Fu, Lei ; Peng, Shifang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-87ee1119bf36c5568e3cd743dc74108cfe203720ad98d355d0935fb4302b24b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Asymptomatic</topic><topic>Bioinformatics</topic><topic>Biomarkers</topic><topic>Biomarkers - metabolism</topic><topic>Biopsy</topic><topic>Cancer therapies</topic><topic>Carcinoma, Hepatocellular - diagnosis</topic><topic>Circular RNA</topic><topic>Gastroenterology and Hepatology</topic><topic>Gene Expression Profiling - methods</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Hepatitis B</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatocellular carcinoma</topic><topic>Hepatoma</topic><topic>Humans</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Medical Genetics</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Metastasis</topic><topic>MicroRNA</topic><topic>MicroRNAs - genetics</topic><topic>miRNA</topic><topic>Molecular Biology</topic><topic>mRNA</topic><topic>Next-generation sequencing</topic><topic>Public Health</topic><topic>Reproducibility of Results</topic><topic>Reverse transcription</topic><topic>RNA, Circular - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>Serum biomarker</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Ying</creatorcontrib><creatorcontrib>Li, Ronghua</creatorcontrib><creatorcontrib>Cheng, Da</creatorcontrib><creatorcontrib>Fu, Xiaoyu</creatorcontrib><creatorcontrib>Fu, Lei</creatorcontrib><creatorcontrib>Peng, Shifang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PeerJ (San Francisco, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Ying</au><au>Li, Ronghua</au><au>Cheng, Da</au><au>Fu, Xiaoyu</au><au>Fu, Lei</au><au>Peng, Shifang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The potential of CircRNA1002 as a biomarker in hepatitis B virus-related hepatocellular carcinoma</atitle><jtitle>PeerJ (San Francisco, CA)</jtitle><addtitle>PeerJ</addtitle><date>2022-06-28</date><risdate>2022</risdate><volume>10</volume><spage>e13640</spage><epage>e13640</epage><pages>e13640-e13640</pages><artnum>e13640</artnum><issn>2167-8359</issn><eissn>2167-8359</eissn><abstract>Although hepatocellular carcinoma (HCC) is the most common type of primary liver cancer, there is a lack of effective diagnostic measures. Circular RNAs (circRNAs) can be used as biomarkers for monitoring the occurrence and development of HCC. However, a convenient and reliable serum circRNA biomarker is not currently available.
CircRNA expression profiles were explored using high-throughput sequencing technology, and targeted circRNAs and mRNAs were validated by quantitative reverse transcription PCR (RT-qPCR). The biological functions of circRNAs were investigated using Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Downstream miRNAs and mRNAs of dysregulated circRNAs were predicted using TargetScan, miRanda, and miRDB; then circRNA-miRNA-mRNA interaction networks were constructed based on sequencing data and the Cancer Genome Atlas (TCGA).
A total of 50,327 circRNAs were identified, with 1,187 circRNAs significantly differentially expressed between hepatitis B virus (HBV)-related HCC and HBV asymptomatic carriers. Among these circRNAs, four (circRNA1002, circRNA7941, circRNA 39338, and circRNA44142) were validated by RT-qPCR as being statistically different either in HCC tissue or serum samples. circRNA1002 was significantly down-regulated in both HCC serum and tissue, indicating its reliability. Bioinformatics analysis showed that circRNA1002-associated genes were enriched in GO terms relating to hormone pathway and cell-cell interaction processes, which are involved in the progression of HCC.
Our circRNA analysis of HCC patients and HBV asymptomatic carriers showed that circRNA1002 may be a reliable serum biomarker for HCC. These results could provide an improved assay for the early detection of HCC.</abstract><cop>United States</cop><pub>PeerJ. Ltd</pub><pmid>35782101</pmid><doi>10.7717/peerj.13640</doi><orcidid>https://orcid.org/0000-0001-7550-1254</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Asymptomatic Bioinformatics Biomarkers Biomarkers - metabolism Biopsy Cancer therapies Carcinoma, Hepatocellular - diagnosis Circular RNA Gastroenterology and Hepatology Gene Expression Profiling - methods Genomes Genomics Hepatitis B Hepatitis B virus Hepatitis B virus - genetics Hepatocellular carcinoma Hepatoma Humans Liver Liver cancer Liver Neoplasms - diagnosis Medical Genetics Medical prognosis Medical research Metastasis MicroRNA MicroRNAs - genetics miRNA Molecular Biology mRNA Next-generation sequencing Public Health Reproducibility of Results Reverse transcription RNA, Circular - genetics RNA, Messenger - genetics Serum biomarker |
title | The potential of CircRNA1002 as a biomarker in hepatitis B virus-related hepatocellular carcinoma |
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