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Methylated RNA Immunoprecipitation Sequencing Reveals the m6A Landscape in Oral Squamous Cell Carcinoma
N6-methyladenosine (m6A) is the most common epigenetic modification existing in eukaryocyte transcripts. However, genes related to m6A modification in oral squamous cell carcinoma (OSCC) are still unclear. Here, methylated RNA immunoprecipitation sequencing (MeRIP-Seq) was performed to map the m6A l...
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Published in: | Journal of immunology research 2022-07, Vol.2022, p.1-13 |
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description | N6-methyladenosine (m6A) is the most common epigenetic modification existing in eukaryocyte transcripts. However, genes related to m6A modification in oral squamous cell carcinoma (OSCC) are still unclear. Here, methylated RNA immunoprecipitation sequencing (MeRIP-Seq) was performed to map the m6A landscape in OSCC and corresponding controls. The m6A peaks are always distributed in the junction of the 3′-untranslated regions (3′-UTRs) and the coding sequences (CDS) of mRNAs, as well as the entire genome of long noncoding RNA (lncRNA). Furthermore, enrichment analysis showed that differentially methylated genes were significantly enriched in NF-kappa B signaling pathway, Hedgehog signaling pathway, etc. In summary, our findings reveal the landscape of m6A modification on mRNAs and lncRNAs in OSCC, which may provide key clues for the precision-targeted therapy of OSCC. |
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However, genes related to m6A modification in oral squamous cell carcinoma (OSCC) are still unclear. Here, methylated RNA immunoprecipitation sequencing (MeRIP-Seq) was performed to map the m6A landscape in OSCC and corresponding controls. The m6A peaks are always distributed in the junction of the 3′-untranslated regions (3′-UTRs) and the coding sequences (CDS) of mRNAs, as well as the entire genome of long noncoding RNA (lncRNA). Furthermore, enrichment analysis showed that differentially methylated genes were significantly enriched in NF-kappa B signaling pathway, Hedgehog signaling pathway, etc. In summary, our findings reveal the landscape of m6A modification on mRNAs and lncRNAs in OSCC, which may provide key clues for the precision-targeted therapy of OSCC.</description><identifier>ISSN: 2314-8861</identifier><identifier>EISSN: 2314-7156</identifier><identifier>DOI: 10.1155/2022/7277583</identifier><identifier>PMID: 35874897</identifier><language>eng</language><publisher>New York: Hindawi</publisher><subject>3' Untranslated regions ; Cancer ; Epigenetics ; Genes ; Genomes ; Hedgehog protein ; Immunology ; Immunoprecipitation ; MicroRNAs ; N6-methyladenosine ; NF-κB protein ; Non-coding RNA ; Ontology ; Oral cancer ; Oral carcinoma ; Oral squamous cell carcinoma ; Ribonucleic acid ; RNA ; Signal transduction ; Software packages ; Squamous cell carcinoma</subject><ispartof>Journal of immunology research, 2022-07, Vol.2022, p.1-13</ispartof><rights>Copyright © 2022 Xi Wang et al.</rights><rights>Copyright © 2022 Xi Wang et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2022 Xi Wang et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-b6b1f51f53d108d48a305fe0abebf7d20373aedd8c113516d2cfeffdd33dd17a3</citedby><cites>FETCH-LOGICAL-c421t-b6b1f51f53d108d48a305fe0abebf7d20373aedd8c113516d2cfeffdd33dd17a3</cites><orcidid>0000-0002-1856-6032 ; 0000-0002-3153-3817</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2693600034/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2693600034?pq-origsite=primo$$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></links><search><contributor>Huang, Jingang</contributor><contributor>Jingang Huang</contributor><creatorcontrib>Wang, Xi</creatorcontrib><creatorcontrib>Wu, Jie</creatorcontrib><creatorcontrib>Zhang, Leyu</creatorcontrib><creatorcontrib>Zhao, Wei</creatorcontrib><creatorcontrib>Deng, Jiayin</creatorcontrib><title>Methylated RNA Immunoprecipitation Sequencing Reveals the m6A Landscape in Oral Squamous Cell Carcinoma</title><title>Journal of immunology research</title><description>N6-methyladenosine (m6A) is the most common epigenetic modification existing in eukaryocyte transcripts. However, genes related to m6A modification in oral squamous cell carcinoma (OSCC) are still unclear. Here, methylated RNA immunoprecipitation sequencing (MeRIP-Seq) was performed to map the m6A landscape in OSCC and corresponding controls. The m6A peaks are always distributed in the junction of the 3′-untranslated regions (3′-UTRs) and the coding sequences (CDS) of mRNAs, as well as the entire genome of long noncoding RNA (lncRNA). Furthermore, enrichment analysis showed that differentially methylated genes were significantly enriched in NF-kappa B signaling pathway, Hedgehog signaling pathway, etc. In summary, our findings reveal the landscape of m6A modification on mRNAs and lncRNAs in OSCC, which may provide key clues for the precision-targeted therapy of OSCC.</description><subject>3' Untranslated regions</subject><subject>Cancer</subject><subject>Epigenetics</subject><subject>Genes</subject><subject>Genomes</subject><subject>Hedgehog protein</subject><subject>Immunology</subject><subject>Immunoprecipitation</subject><subject>MicroRNAs</subject><subject>N6-methyladenosine</subject><subject>NF-κB protein</subject><subject>Non-coding RNA</subject><subject>Ontology</subject><subject>Oral cancer</subject><subject>Oral carcinoma</subject><subject>Oral squamous cell carcinoma</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Signal transduction</subject><subject>Software packages</subject><subject>Squamous cell carcinoma</subject><issn>2314-8861</issn><issn>2314-7156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kl1rFDEUhgdRbKm98wcEvBF0bb6TuRGWxY-F1UKr1yGTnOymzCTbzEyl_96suwj1QggkJM95OHk5TfOa4A-ECHFFMaVXiiolNHvWnFNG-EIRIZ-fzlpLctZcjmPssMCKManly-aMCa24btV5s_0G0-6xtxN4dPN9idbDMKe8L-DiPk52ijmhW7ifIbmYtugGHsD2I5p2gAa5RBub_OjsHlBM6LrYHt3ez3bI84hW0PdoZUuty4N91bwItRAuT_tF8_Pzpx-rr4vN9Zf1arlZOE7JtOhkR4Koi3mCtefaMiwCYNtBF5SnmClmwXvtCGGCSE9dgBC8Z8x7oiy7aNZHr8_2zuxLHGx5NNlG8-cil62xZYquB-Mo5k770PI2cO9ESyjXnSQS02BlcNX18ejaz90A3kGa6g-fSJ--pLgz2_xgWlaj1qQK3p4EJdcIx8kMcXQ1F5ugRmSobDknCitR0Tf_oHd5LqlGdaCYxBgzXqn3R8qVPI4Fwt9mCDaHgTCHgTCngaj4uyO-i8nbX_H_9G-ozbSJ</recordid><startdate>20220715</startdate><enddate>20220715</enddate><creator>Wang, Xi</creator><creator>Wu, Jie</creator><creator>Zhang, Leyu</creator><creator>Zhao, Wei</creator><creator>Deng, Jiayin</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1856-6032</orcidid><orcidid>https://orcid.org/0000-0002-3153-3817</orcidid></search><sort><creationdate>20220715</creationdate><title>Methylated RNA Immunoprecipitation Sequencing Reveals the m6A Landscape in Oral Squamous Cell Carcinoma</title><author>Wang, Xi ; 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However, genes related to m6A modification in oral squamous cell carcinoma (OSCC) are still unclear. Here, methylated RNA immunoprecipitation sequencing (MeRIP-Seq) was performed to map the m6A landscape in OSCC and corresponding controls. The m6A peaks are always distributed in the junction of the 3′-untranslated regions (3′-UTRs) and the coding sequences (CDS) of mRNAs, as well as the entire genome of long noncoding RNA (lncRNA). Furthermore, enrichment analysis showed that differentially methylated genes were significantly enriched in NF-kappa B signaling pathway, Hedgehog signaling pathway, etc. In summary, our findings reveal the landscape of m6A modification on mRNAs and lncRNAs in OSCC, which may provide key clues for the precision-targeted therapy of OSCC.</abstract><cop>New York</cop><pub>Hindawi</pub><pmid>35874897</pmid><doi>10.1155/2022/7277583</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-1856-6032</orcidid><orcidid>https://orcid.org/0000-0002-3153-3817</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated regions Cancer Epigenetics Genes Genomes Hedgehog protein Immunology Immunoprecipitation MicroRNAs N6-methyladenosine NF-κB protein Non-coding RNA Ontology Oral cancer Oral carcinoma Oral squamous cell carcinoma Ribonucleic acid RNA Signal transduction Software packages Squamous cell carcinoma |
title | Methylated RNA Immunoprecipitation Sequencing Reveals the m6A Landscape in Oral Squamous Cell Carcinoma |
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