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Dysregulated microRNA Expression Relevant to TERT Promoter Mutations in Tonsil Cancer—A Pilot Study
Tonsillar squamous cell carcinomas (TSCCs) exhibit high rates of human papillomavirus (HPV) positivity. The expression profiles of microRNA (miRNA), which are small RNA molecules that play pivotal roles in biological processes, in TSCC in relation to the HPV status and cancer-related genetic mutatio...
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Published in: | Life (Basel, Switzerland) Switzerland), 2023-10, Vol.13 (10), p.2090 |
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description | Tonsillar squamous cell carcinomas (TSCCs) exhibit high rates of human papillomavirus (HPV) positivity. The expression profiles of microRNA (miRNA), which are small RNA molecules that play pivotal roles in biological processes, in TSCC in relation to the HPV status and cancer-related genetic mutations are not well investigated. Herein, we expanded our previous research, which was focused on established clinicopathological and genetic mutational data, to profile miRNA expression in TSCC, aiming to identify clinically relevant targets for early diagnosis and therapeutic intervention. The miRNA profiles were analyzed using the nCounter Nanostring miRNA Expression assay in 22 surgically resected TSCC tissues and their contralateral normal tonsil tissues. The TERT promoter (TERTp) gene was the only relevant candidate gene associated with differentially expressed miRNAs in TSCC. Hierarchical clustering analysis revealed high expression levels of hsa-miR-1285-5p, hsa-miR-1203, hsa-miR-663a, hsa-miR-1303, hsa-miR-33a-5p, and hsa-miR-3615 coupled with low expression levels of hsa-miR-3182, hsa-miR-219a-2-3p, and hsa-miR-767-3p, which were associated with HPV-positive TSCC (p = 0.009). Functional enrichment analysis revealed that these dysregulated miRNAs tended to be involved in protein binding (molecular function) and cellular components (biological processes). Therefore, hsa-miR-1285-5p and hsa-miR-663a may be associated with HPV-positive TERTp-mutated tumors and may serve as potential treatment targets and biomarkers for early detection. |
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The expression profiles of microRNA (miRNA), which are small RNA molecules that play pivotal roles in biological processes, in TSCC in relation to the HPV status and cancer-related genetic mutations are not well investigated. Herein, we expanded our previous research, which was focused on established clinicopathological and genetic mutational data, to profile miRNA expression in TSCC, aiming to identify clinically relevant targets for early diagnosis and therapeutic intervention. The miRNA profiles were analyzed using the nCounter Nanostring miRNA Expression assay in 22 surgically resected TSCC tissues and their contralateral normal tonsil tissues. The TERT promoter (TERTp) gene was the only relevant candidate gene associated with differentially expressed miRNAs in TSCC. Hierarchical clustering analysis revealed high expression levels of hsa-miR-1285-5p, hsa-miR-1203, hsa-miR-663a, hsa-miR-1303, hsa-miR-33a-5p, and hsa-miR-3615 coupled with low expression levels of hsa-miR-3182, hsa-miR-219a-2-3p, and hsa-miR-767-3p, which were associated with HPV-positive TSCC (p = 0.009). Functional enrichment analysis revealed that these dysregulated miRNAs tended to be involved in protein binding (molecular function) and cellular components (biological processes). Therefore, hsa-miR-1285-5p and hsa-miR-663a may be associated with HPV-positive TERTp-mutated tumors and may serve as potential treatment targets and biomarkers for early detection.</description><identifier>ISSN: 2075-1729</identifier><identifier>EISSN: 2075-1729</identifier><identifier>DOI: 10.3390/life13102090</identifier><identifier>PMID: 37895471</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Biological activity ; Biomarkers ; Cancer ; Chemotherapy ; Cluster analysis ; Clustering ; Epigenetics ; Gene expression ; Gene set enrichment analysis ; Genomes ; Genomics ; hsa-miR-1285-5p ; Human papillomavirus ; Kinases ; Metastasis ; MicroRNAs ; miRNA ; miRNAs ; Mutation ; oropharynx ; Radiation therapy ; Ribonucleic acid ; RNA ; Software ; Squamous cell carcinoma ; TERT promoter gene ; Tonsil ; Tonsillar carcinoma ; Tumors</subject><ispartof>Life (Basel, Switzerland), 2023-10, Vol.13 (10), p.2090</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c413t-9ea24b47cf008f339ec99416122ebf4756f85ad857c9e27f965704316bad1d503</cites><orcidid>0000-0001-9245-8657 ; 0000-0002-2441-0448</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2882597167/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2882597167?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids></links><search><creatorcontrib>Kwon, Mi Jung</creatorcontrib><creatorcontrib>Park, Ha Young</creatorcontrib><creatorcontrib>Lee, Joong Seob</creatorcontrib><creatorcontrib>Kim, Eun Soo</creatorcontrib><creatorcontrib>Kim, Nan Young</creatorcontrib><creatorcontrib>Nam, Eun Sook</creatorcontrib><creatorcontrib>Cho, Seong Jin</creatorcontrib><creatorcontrib>Kang, Ho Suk</creatorcontrib><title>Dysregulated microRNA Expression Relevant to TERT Promoter Mutations in Tonsil Cancer—A Pilot Study</title><title>Life (Basel, Switzerland)</title><description>Tonsillar squamous cell carcinomas (TSCCs) exhibit high rates of human papillomavirus (HPV) positivity. The expression profiles of microRNA (miRNA), which are small RNA molecules that play pivotal roles in biological processes, in TSCC in relation to the HPV status and cancer-related genetic mutations are not well investigated. Herein, we expanded our previous research, which was focused on established clinicopathological and genetic mutational data, to profile miRNA expression in TSCC, aiming to identify clinically relevant targets for early diagnosis and therapeutic intervention. The miRNA profiles were analyzed using the nCounter Nanostring miRNA Expression assay in 22 surgically resected TSCC tissues and their contralateral normal tonsil tissues. The TERT promoter (TERTp) gene was the only relevant candidate gene associated with differentially expressed miRNAs in TSCC. Hierarchical clustering analysis revealed high expression levels of hsa-miR-1285-5p, hsa-miR-1203, hsa-miR-663a, hsa-miR-1303, hsa-miR-33a-5p, and hsa-miR-3615 coupled with low expression levels of hsa-miR-3182, hsa-miR-219a-2-3p, and hsa-miR-767-3p, which were associated with HPV-positive TSCC (p = 0.009). Functional enrichment analysis revealed that these dysregulated miRNAs tended to be involved in protein binding (molecular function) and cellular components (biological processes). Therefore, hsa-miR-1285-5p and hsa-miR-663a may be associated with HPV-positive TERTp-mutated tumors and may serve as potential treatment targets and biomarkers for early detection.</description><subject>Biological activity</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Cluster analysis</subject><subject>Clustering</subject><subject>Epigenetics</subject><subject>Gene expression</subject><subject>Gene set enrichment analysis</subject><subject>Genomes</subject><subject>Genomics</subject><subject>hsa-miR-1285-5p</subject><subject>Human papillomavirus</subject><subject>Kinases</subject><subject>Metastasis</subject><subject>MicroRNAs</subject><subject>miRNA</subject><subject>miRNAs</subject><subject>Mutation</subject><subject>oropharynx</subject><subject>Radiation therapy</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Software</subject><subject>Squamous cell carcinoma</subject><subject>TERT promoter gene</subject><subject>Tonsil</subject><subject>Tonsillar carcinoma</subject><subject>Tumors</subject><issn>2075-1729</issn><issn>2075-1729</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks1uEzEQgFcIRKvSGw9giQsHAv73-oSiNJRKBaoQzpbXOxscedfB9lbk1ofgCXkSNqRCLb6M5fn0aTwzVfWS4LeMafwu-A4II5hijZ9UpxQrMSOK6qcP7ifVec5bPB0piKz58-qEqVoLrshpBRf7nGAzBlugRb13Ka4-z9Hy5y5Bzj4OaAUBbu1QUIlovVyt0U2KfSyQ0Kex2DIhGfkBrafoA1rYwUH6ffdrjm58iAV9LWO7f1E962zIcH4fz6pvH5brxcfZ9ZfLq8X8euY4YWWmwVLecOU6jOtu-iA4rTmRhFJoOq6E7Gph21oop4GqTkuhMGdENrYlrcDsrLo6ettot2aXfG_T3kTrzd-HmDbGpuJdAKOlsyA571wD3FmqBe0o440AW7e2PbjeH127semhdTCUZMMj6ePM4L-bTbw1BEtcC30wvL43pPhjhFxM77ODEOwAccyG1jUTinBCJ_TVf-g2jmmYenWgqNCKSDVRb47UNKU8ja37Vw3B5rAP5uE-sD_e1agJ</recordid><startdate>20231020</startdate><enddate>20231020</enddate><creator>Kwon, Mi Jung</creator><creator>Park, Ha Young</creator><creator>Lee, Joong Seob</creator><creator>Kim, Eun Soo</creator><creator>Kim, Nan Young</creator><creator>Nam, Eun Sook</creator><creator>Cho, Seong Jin</creator><creator>Kang, Ho Suk</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9245-8657</orcidid><orcidid>https://orcid.org/0000-0002-2441-0448</orcidid></search><sort><creationdate>20231020</creationdate><title>Dysregulated microRNA Expression Relevant to TERT Promoter Mutations in Tonsil Cancer—A Pilot Study</title><author>Kwon, Mi Jung ; 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The expression profiles of microRNA (miRNA), which are small RNA molecules that play pivotal roles in biological processes, in TSCC in relation to the HPV status and cancer-related genetic mutations are not well investigated. Herein, we expanded our previous research, which was focused on established clinicopathological and genetic mutational data, to profile miRNA expression in TSCC, aiming to identify clinically relevant targets for early diagnosis and therapeutic intervention. The miRNA profiles were analyzed using the nCounter Nanostring miRNA Expression assay in 22 surgically resected TSCC tissues and their contralateral normal tonsil tissues. The TERT promoter (TERTp) gene was the only relevant candidate gene associated with differentially expressed miRNAs in TSCC. Hierarchical clustering analysis revealed high expression levels of hsa-miR-1285-5p, hsa-miR-1203, hsa-miR-663a, hsa-miR-1303, hsa-miR-33a-5p, and hsa-miR-3615 coupled with low expression levels of hsa-miR-3182, hsa-miR-219a-2-3p, and hsa-miR-767-3p, which were associated with HPV-positive TSCC (p = 0.009). Functional enrichment analysis revealed that these dysregulated miRNAs tended to be involved in protein binding (molecular function) and cellular components (biological processes). Therefore, hsa-miR-1285-5p and hsa-miR-663a may be associated with HPV-positive TERTp-mutated tumors and may serve as potential treatment targets and biomarkers for early detection.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>37895471</pmid><doi>10.3390/life13102090</doi><orcidid>https://orcid.org/0000-0001-9245-8657</orcidid><orcidid>https://orcid.org/0000-0002-2441-0448</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biological activity Biomarkers Cancer Chemotherapy Cluster analysis Clustering Epigenetics Gene expression Gene set enrichment analysis Genomes Genomics hsa-miR-1285-5p Human papillomavirus Kinases Metastasis MicroRNAs miRNA miRNAs Mutation oropharynx Radiation therapy Ribonucleic acid RNA Software Squamous cell carcinoma TERT promoter gene Tonsil Tonsillar carcinoma Tumors |
title | Dysregulated microRNA Expression Relevant to TERT Promoter Mutations in Tonsil Cancer—A Pilot Study |
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