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Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing
Postoperative recurrence of colorectal cancer (CRC) eventually leads to therapeutic failure; therefore, treatment strategies based on accurate prediction of recurrence are urgently required. To identify biomarkers that can predict treatment outcomes, we compared the mutational profiles of surgically...
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Published in: | Cancer medicine (Malden, MA) MA), 2022-09, Vol.11 (18), p.3457-3470 |
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creator | Kishigami, Fumishi Tanaka, Yosuke Yamamoto, Yoko Ueno, Toshihide Kojima, Shinya Sato, Kazuhito Inoue, Satoshi Sugaya, Saori Ishihara, Soichiro Mano, Hiroyuki Kawazu, Masahito |
description | Postoperative recurrence of colorectal cancer (CRC) eventually leads to therapeutic failure; therefore, treatment strategies based on accurate prediction of recurrence are urgently required. To identify biomarkers that can predict treatment outcomes, we compared the mutational profiles of surgically resected specimens from patients with recurrent cancer with those from patients with non‐recurrent cancer. Target sequencing, whole‐exome sequencing (WES), or whole‐genome sequencing (WGS) was performed on 89 and 58 tumors from recurrent and non‐recurrent cases, respectively. WGS revealed the driver mutations that were not detected with target sequencing or WES, including the structural variations affecting ZFP36L2. Loss of function of ZFP36L2 was frequently observed in primary tumors from recurrent cases. Furthermore, the recurrence‐free survival of patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function. In summary, the study demonstrated that detailed genomic analysis could help improve precision medicine for CRC.
Loss of function of ZFP36L2 was frequently observed in recurrent colorectal cancers. Furthermore, the recurrence‐free survival of colorectal cancer patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function. |
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Loss of function of ZFP36L2 was frequently observed in recurrent colorectal cancers. Furthermore, the recurrence‐free survival of colorectal cancer patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function.</description><identifier>ISSN: 2045-7634</identifier><identifier>EISSN: 2045-7634</identifier><identifier>DOI: 10.1002/cam4.4710</identifier><identifier>PMID: 35343095</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Antigens ; Automation ; Biomarkers ; Cancer ; Chemotherapy ; Cloning ; Colorectal cancer ; Colorectal carcinoma ; Genes ; Genomes ; Genomic analysis ; Mutation ; Patients ; Precision medicine ; Survival analysis ; Tumors ; whole genome sequence ; ZFP36L2</subject><ispartof>Cancer medicine (Malden, MA), 2022-09, Vol.11 (18), p.3457-3470</ispartof><rights>2022 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.</rights><rights>2022. 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-c5200-424b6e061d47a7e4f72217acc81e51e831dc723b3069e6f591e99839861954673</citedby><cites>FETCH-LOGICAL-c5200-424b6e061d47a7e4f72217acc81e51e831dc723b3069e6f591e99839861954673</cites><orcidid>0000-0003-4645-0181 ; 0000-0003-4146-3629</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2715808691/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2715808691?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,11562,25753,27924,27925,37012,37013,44590,46052,46476,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35343095$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishigami, Fumishi</creatorcontrib><creatorcontrib>Tanaka, Yosuke</creatorcontrib><creatorcontrib>Yamamoto, Yoko</creatorcontrib><creatorcontrib>Ueno, Toshihide</creatorcontrib><creatorcontrib>Kojima, Shinya</creatorcontrib><creatorcontrib>Sato, Kazuhito</creatorcontrib><creatorcontrib>Inoue, Satoshi</creatorcontrib><creatorcontrib>Sugaya, Saori</creatorcontrib><creatorcontrib>Ishihara, Soichiro</creatorcontrib><creatorcontrib>Mano, Hiroyuki</creatorcontrib><creatorcontrib>Kawazu, Masahito</creatorcontrib><title>Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing</title><title>Cancer medicine (Malden, MA)</title><addtitle>Cancer Med</addtitle><description>Postoperative recurrence of colorectal cancer (CRC) eventually leads to therapeutic failure; therefore, treatment strategies based on accurate prediction of recurrence are urgently required. To identify biomarkers that can predict treatment outcomes, we compared the mutational profiles of surgically resected specimens from patients with recurrent cancer with those from patients with non‐recurrent cancer. Target sequencing, whole‐exome sequencing (WES), or whole‐genome sequencing (WGS) was performed on 89 and 58 tumors from recurrent and non‐recurrent cases, respectively. WGS revealed the driver mutations that were not detected with target sequencing or WES, including the structural variations affecting ZFP36L2. Loss of function of ZFP36L2 was frequently observed in primary tumors from recurrent cases. Furthermore, the recurrence‐free survival of patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function. In summary, the study demonstrated that detailed genomic analysis could help improve precision medicine for CRC.
Loss of function of ZFP36L2 was frequently observed in recurrent colorectal cancers. Furthermore, the recurrence‐free survival of colorectal cancer patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function.</description><subject>Antigens</subject><subject>Automation</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Cloning</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomic analysis</subject><subject>Mutation</subject><subject>Patients</subject><subject>Precision medicine</subject><subject>Survival analysis</subject><subject>Tumors</subject><subject>whole genome sequence</subject><subject>ZFP36L2</subject><issn>2045-7634</issn><issn>2045-7634</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kU1v1DAQhqMKRKvSA3-gssQFDtv1V-z4WK0KRCri0p4tZzJZeUniYCdAJX48TrdUCAlfbI0fP57RWxRvGL1ilPItuEFeSc3oSXHGqSw3Wgn54q_zaXGR0oHmpSlXmr0qTkUppKCmPCt-3fyc-hDd7MNIQkemiK2H2X9H0vgwuPgVYyJdiGQKaQ4Trmi-jAhLjDgCrq_S7PZI6npb1zWBkIUIs-sJuAxEsiQ_7skexzB4IAm_LflhLr0uXnauT3jxtJ8X9x9u7nafNrdfPta769sNlJzSjeSyUUgVa6V2GmWnOWfaAVQMS4aVYC1oLhpBlUHVlYahMZUwlWKmlEqL86I-etvgDnaKPs_1YIPz9rEQ4t66OHvo0WraVbSioGUnpQPdADMUnFGClVpUXXa9O7qmGPIcabaDT4B970YMS7JcSSkUyy1m9O0_6CEsccyTWq5Zmf9RhmXq_ZGCGFKK2D03yKhdE7ZrwnZNOLOXT8alGbB9Jv_kmYHtEfjhe3z4v8nurj_LR-VvhTiuGg</recordid><startdate>202209</startdate><enddate>202209</enddate><creator>Kishigami, Fumishi</creator><creator>Tanaka, Yosuke</creator><creator>Yamamoto, Yoko</creator><creator>Ueno, Toshihide</creator><creator>Kojima, Shinya</creator><creator>Sato, Kazuhito</creator><creator>Inoue, Satoshi</creator><creator>Sugaya, Saori</creator><creator>Ishihara, Soichiro</creator><creator>Mano, Hiroyuki</creator><creator>Kawazu, Masahito</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4645-0181</orcidid><orcidid>https://orcid.org/0000-0003-4146-3629</orcidid></search><sort><creationdate>202209</creationdate><title>Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing</title><author>Kishigami, Fumishi ; 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therefore, treatment strategies based on accurate prediction of recurrence are urgently required. To identify biomarkers that can predict treatment outcomes, we compared the mutational profiles of surgically resected specimens from patients with recurrent cancer with those from patients with non‐recurrent cancer. Target sequencing, whole‐exome sequencing (WES), or whole‐genome sequencing (WGS) was performed on 89 and 58 tumors from recurrent and non‐recurrent cases, respectively. WGS revealed the driver mutations that were not detected with target sequencing or WES, including the structural variations affecting ZFP36L2. Loss of function of ZFP36L2 was frequently observed in primary tumors from recurrent cases. Furthermore, the recurrence‐free survival of patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function. In summary, the study demonstrated that detailed genomic analysis could help improve precision medicine for CRC.
Loss of function of ZFP36L2 was frequently observed in recurrent colorectal cancers. Furthermore, the recurrence‐free survival of colorectal cancer patients with loss of function of ZFP36L2 was significantly shorter relative to patients with no loss of ZFP36L2 function.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>35343095</pmid><doi>10.1002/cam4.4710</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-4645-0181</orcidid><orcidid>https://orcid.org/0000-0003-4146-3629</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Automation Biomarkers Cancer Chemotherapy Cloning Colorectal cancer Colorectal carcinoma Genes Genomes Genomic analysis Mutation Patients Precision medicine Survival analysis Tumors whole genome sequence ZFP36L2 |
title | Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing |
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