The impact of ARID1A mutation on molecular characteristics in colorectal cancer
ARID1A is a key subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex which regulates dynamic repositioning of nucleosomes to repair DNA damage. Only small pilot studies have evaluated the role of ARID1A mutation in colorectal cancer (CRC). The aim of the present study was to explore the p...
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creator | Tokunaga, Ryuma Xiu, Joanne Goldberg, Richard M. Philip, Philip A. Seeber, Andreas Battaglin, Francesca Arai, Hiroyuki Lo, Jae Ho Naseem, Madiha Puccini, Alberto Berger, Martin D. Soni, Shivani Zhang, Wu Chen, Sting Hwang, Jimmy J. Shields, Anthony F. Marshall, John L. Baba, Hideo Korn, W.Michael Lenz, Heinz-Josef |
description | ARID1A is a key subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex which regulates dynamic repositioning of nucleosomes to repair DNA damage. Only small pilot studies have evaluated the role of ARID1A mutation in colorectal cancer (CRC). The aim of the present study was to explore the potential impact of ARID1A mutation on clinicopathological and molecular characteristics in CRC.
We used integrated data sets of 7978 CRC cases (one data set from a clinical laboratory improvement amendments [CLIA]-certified laboratory and three independent published data sets). The associations of ARID1A mutation with molecular characteristics including immune profile (the status of microsatellite instability [MSI], tumour mutational burden [TMB], programmed death ligand 1 [PD-L1] and estimated infiltrating immune cells), clinicopathological features and related pathways were analysed using next-generation sequencing, RNA sequencing and immunohistochemistry.
ARID1A mutant samples had more genomically unstable tumour features (MSI-high and TMB-high) and exhibited more characteristics of a T-cell–inflamed microenvironment (PD-L1 expression and high estimated infiltrating cytotoxic T lymphocytes [CTLs]) than ARID1A wild-type samples in the discovery and validation cohorts. Even ARID1A mutant samples without MSI-high status were TMB-high, had high levels of PD-L1 expression and high estimated infiltrating CTLs. ARID1A mutations were more common with right-sided primary and earlier stage tumours. ARID1A mutant tumours mainly had co-occurring gene mutations related to chromatin modifying, DNA repair, WNT signalling and epidermal growth factor receptor inhibitor resistance pathways, and ARID1A mutations strongly regulated DNA repair pathways. Key genes for chemotherapy/radiotherapy sensitivity were suppressed in ARID1A mutant samples.
Our findings may provide novel insights to develop individualised approaches for treatment of CRC based on ARID1A mutation status.
•The impact of ARID1A mutations was analysed using 7978 colorectal cancer samples.•ARID1A mutation was linked to immune activation, right-sided tumour and early stage.•ARID1A mutation may be a biomarker for chemotherapy/radiotherapy and targeted therapy. |
doi_str_mv | 10.1016/j.ejca.2020.09.006 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8009046</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0959804920304895</els_id><sourcerecordid>2452982911</sourcerecordid><originalsourceid>FETCH-LOGICAL-c549t-69c6d4c1b0c9dafe24cb3953700222d92327b0c622bb17d8a8b747db8e65287a3</originalsourceid><addsrcrecordid>eNp9kdGL1DAQxoMo3t7pP-CDFHzxpXWSpk0CIiynpwcHB3I-h3Q666a0zZq0B_73ZtnzUB-EgcDMbz4y38fYKw4VB96-Gyoa0FUCBFRgKoD2CdtwrUwJuhFP2QZMY0oN0pyx85QGAFBawnN2VteQ20pu2O3dngo_HRwuRdgV26_XH_m2mNbFLT7MRa4pjITr6GKBexczR9GnxWMq_FxgGEMkXNxYoJuR4gv2bOfGRC8f3gv27erT3eWX8ub28_Xl9qbERpqlbA22vUTeAZre7UhI7GrT1ApACNEbUQuVZ60QXcdVr53ulFR9p6lthFauvmAfTrqHtZuoR5qX6EZ7iH5y8acNztu_J7Pf2-_h3moAA7LNAm8fBGL4sVJa7OQT0ji6mcKarJCNMFoYzjP65h90CGuc83mZanVtgNdNpsSJwhhSirR7_AwHe8zLDvaYlz3mZcHYnFdeev3nGY8rvwPKwPsTQNnMe0_RJvSUne790XfbB_8__V8KB6ZB</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2468390135</pqid></control><display><type>article</type><title>The impact of ARID1A mutation on molecular characteristics in colorectal cancer</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Tokunaga, Ryuma ; Xiu, Joanne ; Goldberg, Richard M. ; Philip, Philip A. ; Seeber, Andreas ; Battaglin, Francesca ; Arai, Hiroyuki ; Lo, Jae Ho ; Naseem, Madiha ; Puccini, Alberto ; Berger, Martin D. ; Soni, Shivani ; Zhang, Wu ; Chen, Sting ; Hwang, Jimmy J. ; Shields, Anthony F. ; Marshall, John L. ; Baba, Hideo ; Korn, W.Michael ; Lenz, Heinz-Josef</creator><creatorcontrib>Tokunaga, Ryuma ; Xiu, Joanne ; Goldberg, Richard M. ; Philip, Philip A. ; Seeber, Andreas ; Battaglin, Francesca ; Arai, Hiroyuki ; Lo, Jae Ho ; Naseem, Madiha ; Puccini, Alberto ; Berger, Martin D. ; Soni, Shivani ; Zhang, Wu ; Chen, Sting ; Hwang, Jimmy J. ; Shields, Anthony F. ; Marshall, John L. ; Baba, Hideo ; Korn, W.Michael ; Lenz, Heinz-Josef</creatorcontrib><description>ARID1A is a key subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex which regulates dynamic repositioning of nucleosomes to repair DNA damage. Only small pilot studies have evaluated the role of ARID1A mutation in colorectal cancer (CRC). The aim of the present study was to explore the potential impact of ARID1A mutation on clinicopathological and molecular characteristics in CRC.
We used integrated data sets of 7978 CRC cases (one data set from a clinical laboratory improvement amendments [CLIA]-certified laboratory and three independent published data sets). The associations of ARID1A mutation with molecular characteristics including immune profile (the status of microsatellite instability [MSI], tumour mutational burden [TMB], programmed death ligand 1 [PD-L1] and estimated infiltrating immune cells), clinicopathological features and related pathways were analysed using next-generation sequencing, RNA sequencing and immunohistochemistry.
ARID1A mutant samples had more genomically unstable tumour features (MSI-high and TMB-high) and exhibited more characteristics of a T-cell–inflamed microenvironment (PD-L1 expression and high estimated infiltrating cytotoxic T lymphocytes [CTLs]) than ARID1A wild-type samples in the discovery and validation cohorts. Even ARID1A mutant samples without MSI-high status were TMB-high, had high levels of PD-L1 expression and high estimated infiltrating CTLs. ARID1A mutations were more common with right-sided primary and earlier stage tumours. ARID1A mutant tumours mainly had co-occurring gene mutations related to chromatin modifying, DNA repair, WNT signalling and epidermal growth factor receptor inhibitor resistance pathways, and ARID1A mutations strongly regulated DNA repair pathways. Key genes for chemotherapy/radiotherapy sensitivity were suppressed in ARID1A mutant samples.
Our findings may provide novel insights to develop individualised approaches for treatment of CRC based on ARID1A mutation status.
•The impact of ARID1A mutations was analysed using 7978 colorectal cancer samples.•ARID1A mutation was linked to immune activation, right-sided tumour and early stage.•ARID1A mutation may be a biomarker for chemotherapy/radiotherapy and targeted therapy.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2020.09.006</identifier><identifier>PMID: 33080474</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Apoptosis ; ARID1A ; Cancer ; Chemotherapy ; Chromatin ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - immunology ; Cytotoxicity ; Data integration ; Datasets ; Deoxyribonucleic acid ; DNA ; DNA damage ; DNA repair ; DNA Repair - genetics ; DNA Repair - immunology ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - immunology ; Epidermal growth factor ; Female ; Gene sequencing ; Growth factors ; Humans ; Immune profile ; Immune system ; Immunohistochemistry ; Immunohistochemistry - methods ; Inflammation ; Laboratories ; Lymphocytes ; Lymphocytes T ; Male ; Microsatellite instability ; Middle Aged ; Molecular profile ; Mutants ; Mutation ; Mutation - genetics ; Mutation - immunology ; Next-generation sequencing ; Nucleosomes ; PD-L1 protein ; Radiation therapy ; Repair ; Resistance factors ; Ribonucleic acid ; Right-sided location ; RNA ; Signal transduction ; Sucrose ; Sugar ; SWI/SNF complex ; T-Lymphocytes, Cytotoxic - immunology ; Transcription Factors - genetics ; Transcription Factors - immunology ; Tumor Microenvironment - genetics ; Tumor Microenvironment - immunology ; Tumors ; Wnt protein ; Young Adult</subject><ispartof>European journal of cancer (1990), 2020-11, Vol.140, p.119-129</ispartof><rights>2020 Elsevier Ltd</rights><rights>Copyright © 2020 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Nov 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-69c6d4c1b0c9dafe24cb3953700222d92327b0c622bb17d8a8b747db8e65287a3</citedby><cites>FETCH-LOGICAL-c549t-69c6d4c1b0c9dafe24cb3953700222d92327b0c622bb17d8a8b747db8e65287a3</cites><orcidid>0000-0002-2492-4043 ; 0000-0003-0308-8223 ; 0000-0002-6368-4177 ; 0000-0002-9869-0163 ; 0000-0002-9285-3849</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0959804920304895$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33080474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tokunaga, Ryuma</creatorcontrib><creatorcontrib>Xiu, Joanne</creatorcontrib><creatorcontrib>Goldberg, Richard M.</creatorcontrib><creatorcontrib>Philip, Philip A.</creatorcontrib><creatorcontrib>Seeber, Andreas</creatorcontrib><creatorcontrib>Battaglin, Francesca</creatorcontrib><creatorcontrib>Arai, Hiroyuki</creatorcontrib><creatorcontrib>Lo, Jae Ho</creatorcontrib><creatorcontrib>Naseem, Madiha</creatorcontrib><creatorcontrib>Puccini, Alberto</creatorcontrib><creatorcontrib>Berger, Martin D.</creatorcontrib><creatorcontrib>Soni, Shivani</creatorcontrib><creatorcontrib>Zhang, Wu</creatorcontrib><creatorcontrib>Chen, Sting</creatorcontrib><creatorcontrib>Hwang, Jimmy J.</creatorcontrib><creatorcontrib>Shields, Anthony F.</creatorcontrib><creatorcontrib>Marshall, John L.</creatorcontrib><creatorcontrib>Baba, Hideo</creatorcontrib><creatorcontrib>Korn, W.Michael</creatorcontrib><creatorcontrib>Lenz, Heinz-Josef</creatorcontrib><title>The impact of ARID1A mutation on molecular characteristics in colorectal cancer</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>ARID1A is a key subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex which regulates dynamic repositioning of nucleosomes to repair DNA damage. Only small pilot studies have evaluated the role of ARID1A mutation in colorectal cancer (CRC). The aim of the present study was to explore the potential impact of ARID1A mutation on clinicopathological and molecular characteristics in CRC.
We used integrated data sets of 7978 CRC cases (one data set from a clinical laboratory improvement amendments [CLIA]-certified laboratory and three independent published data sets). The associations of ARID1A mutation with molecular characteristics including immune profile (the status of microsatellite instability [MSI], tumour mutational burden [TMB], programmed death ligand 1 [PD-L1] and estimated infiltrating immune cells), clinicopathological features and related pathways were analysed using next-generation sequencing, RNA sequencing and immunohistochemistry.
ARID1A mutant samples had more genomically unstable tumour features (MSI-high and TMB-high) and exhibited more characteristics of a T-cell–inflamed microenvironment (PD-L1 expression and high estimated infiltrating cytotoxic T lymphocytes [CTLs]) than ARID1A wild-type samples in the discovery and validation cohorts. Even ARID1A mutant samples without MSI-high status were TMB-high, had high levels of PD-L1 expression and high estimated infiltrating CTLs. ARID1A mutations were more common with right-sided primary and earlier stage tumours. ARID1A mutant tumours mainly had co-occurring gene mutations related to chromatin modifying, DNA repair, WNT signalling and epidermal growth factor receptor inhibitor resistance pathways, and ARID1A mutations strongly regulated DNA repair pathways. Key genes for chemotherapy/radiotherapy sensitivity were suppressed in ARID1A mutant samples.
Our findings may provide novel insights to develop individualised approaches for treatment of CRC based on ARID1A mutation status.
•The impact of ARID1A mutations was analysed using 7978 colorectal cancer samples.•ARID1A mutation was linked to immune activation, right-sided tumour and early stage.•ARID1A mutation may be a biomarker for chemotherapy/radiotherapy and targeted therapy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Apoptosis</subject><subject>ARID1A</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Chromatin</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - immunology</subject><subject>Cytotoxicity</subject><subject>Data integration</subject><subject>Datasets</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA repair</subject><subject>DNA Repair - genetics</subject><subject>DNA Repair - immunology</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - immunology</subject><subject>Epidermal growth factor</subject><subject>Female</subject><subject>Gene sequencing</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Immune profile</subject><subject>Immune system</subject><subject>Immunohistochemistry</subject><subject>Immunohistochemistry - methods</subject><subject>Inflammation</subject><subject>Laboratories</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Microsatellite instability</subject><subject>Middle Aged</subject><subject>Molecular profile</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Mutation - genetics</subject><subject>Mutation - immunology</subject><subject>Next-generation sequencing</subject><subject>Nucleosomes</subject><subject>PD-L1 protein</subject><subject>Radiation therapy</subject><subject>Repair</subject><subject>Resistance factors</subject><subject>Ribonucleic acid</subject><subject>Right-sided location</subject><subject>RNA</subject><subject>Signal transduction</subject><subject>Sucrose</subject><subject>Sugar</subject><subject>SWI/SNF complex</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - immunology</subject><subject>Tumor Microenvironment - genetics</subject><subject>Tumor Microenvironment - immunology</subject><subject>Tumors</subject><subject>Wnt protein</subject><subject>Young Adult</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kdGL1DAQxoMo3t7pP-CDFHzxpXWSpk0CIiynpwcHB3I-h3Q666a0zZq0B_73ZtnzUB-EgcDMbz4y38fYKw4VB96-Gyoa0FUCBFRgKoD2CdtwrUwJuhFP2QZMY0oN0pyx85QGAFBawnN2VteQ20pu2O3dngo_HRwuRdgV26_XH_m2mNbFLT7MRa4pjITr6GKBexczR9GnxWMq_FxgGEMkXNxYoJuR4gv2bOfGRC8f3gv27erT3eWX8ub28_Xl9qbERpqlbA22vUTeAZre7UhI7GrT1ApACNEbUQuVZ60QXcdVr53ulFR9p6lthFauvmAfTrqHtZuoR5qX6EZ7iH5y8acNztu_J7Pf2-_h3moAA7LNAm8fBGL4sVJa7OQT0ji6mcKarJCNMFoYzjP65h90CGuc83mZanVtgNdNpsSJwhhSirR7_AwHe8zLDvaYlz3mZcHYnFdeev3nGY8rvwPKwPsTQNnMe0_RJvSUne790XfbB_8__V8KB6ZB</recordid><startdate>20201101</startdate><enddate>20201101</enddate><creator>Tokunaga, Ryuma</creator><creator>Xiu, Joanne</creator><creator>Goldberg, Richard M.</creator><creator>Philip, Philip A.</creator><creator>Seeber, Andreas</creator><creator>Battaglin, Francesca</creator><creator>Arai, Hiroyuki</creator><creator>Lo, Jae Ho</creator><creator>Naseem, Madiha</creator><creator>Puccini, Alberto</creator><creator>Berger, Martin D.</creator><creator>Soni, Shivani</creator><creator>Zhang, Wu</creator><creator>Chen, Sting</creator><creator>Hwang, Jimmy J.</creator><creator>Shields, Anthony F.</creator><creator>Marshall, John L.</creator><creator>Baba, Hideo</creator><creator>Korn, W.Michael</creator><creator>Lenz, Heinz-Josef</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2492-4043</orcidid><orcidid>https://orcid.org/0000-0003-0308-8223</orcidid><orcidid>https://orcid.org/0000-0002-6368-4177</orcidid><orcidid>https://orcid.org/0000-0002-9869-0163</orcidid><orcidid>https://orcid.org/0000-0002-9285-3849</orcidid></search><sort><creationdate>20201101</creationdate><title>The impact of ARID1A mutation on molecular characteristics in colorectal cancer</title><author>Tokunaga, Ryuma ; Xiu, Joanne ; Goldberg, Richard M. ; Philip, Philip A. ; Seeber, Andreas ; Battaglin, Francesca ; Arai, Hiroyuki ; Lo, Jae Ho ; Naseem, Madiha ; Puccini, Alberto ; Berger, Martin D. ; Soni, Shivani ; Zhang, Wu ; Chen, Sting ; Hwang, Jimmy J. ; Shields, Anthony F. ; Marshall, John L. ; Baba, Hideo ; Korn, W.Michael ; Lenz, Heinz-Josef</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-69c6d4c1b0c9dafe24cb3953700222d92327b0c622bb17d8a8b747db8e65287a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Apoptosis</topic><topic>ARID1A</topic><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Chromatin</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - immunology</topic><topic>Cytotoxicity</topic><topic>Data integration</topic><topic>Datasets</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA damage</topic><topic>DNA repair</topic><topic>DNA Repair - genetics</topic><topic>DNA Repair - immunology</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - immunology</topic><topic>Epidermal growth factor</topic><topic>Female</topic><topic>Gene sequencing</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Immune profile</topic><topic>Immune system</topic><topic>Immunohistochemistry</topic><topic>Immunohistochemistry - methods</topic><topic>Inflammation</topic><topic>Laboratories</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Microsatellite instability</topic><topic>Middle Aged</topic><topic>Molecular profile</topic><topic>Mutants</topic><topic>Mutation</topic><topic>Mutation - genetics</topic><topic>Mutation - immunology</topic><topic>Next-generation sequencing</topic><topic>Nucleosomes</topic><topic>PD-L1 protein</topic><topic>Radiation therapy</topic><topic>Repair</topic><topic>Resistance factors</topic><topic>Ribonucleic acid</topic><topic>Right-sided location</topic><topic>RNA</topic><topic>Signal transduction</topic><topic>Sucrose</topic><topic>Sugar</topic><topic>SWI/SNF complex</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - immunology</topic><topic>Tumor Microenvironment - genetics</topic><topic>Tumor Microenvironment - immunology</topic><topic>Tumors</topic><topic>Wnt protein</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tokunaga, Ryuma</creatorcontrib><creatorcontrib>Xiu, Joanne</creatorcontrib><creatorcontrib>Goldberg, Richard M.</creatorcontrib><creatorcontrib>Philip, Philip A.</creatorcontrib><creatorcontrib>Seeber, Andreas</creatorcontrib><creatorcontrib>Battaglin, Francesca</creatorcontrib><creatorcontrib>Arai, Hiroyuki</creatorcontrib><creatorcontrib>Lo, Jae Ho</creatorcontrib><creatorcontrib>Naseem, Madiha</creatorcontrib><creatorcontrib>Puccini, Alberto</creatorcontrib><creatorcontrib>Berger, Martin D.</creatorcontrib><creatorcontrib>Soni, Shivani</creatorcontrib><creatorcontrib>Zhang, Wu</creatorcontrib><creatorcontrib>Chen, Sting</creatorcontrib><creatorcontrib>Hwang, Jimmy J.</creatorcontrib><creatorcontrib>Shields, Anthony F.</creatorcontrib><creatorcontrib>Marshall, John L.</creatorcontrib><creatorcontrib>Baba, Hideo</creatorcontrib><creatorcontrib>Korn, W.Michael</creatorcontrib><creatorcontrib>Lenz, Heinz-Josef</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tokunaga, Ryuma</au><au>Xiu, Joanne</au><au>Goldberg, Richard M.</au><au>Philip, Philip A.</au><au>Seeber, Andreas</au><au>Battaglin, Francesca</au><au>Arai, Hiroyuki</au><au>Lo, Jae Ho</au><au>Naseem, Madiha</au><au>Puccini, Alberto</au><au>Berger, Martin D.</au><au>Soni, Shivani</au><au>Zhang, Wu</au><au>Chen, Sting</au><au>Hwang, Jimmy J.</au><au>Shields, Anthony F.</au><au>Marshall, John L.</au><au>Baba, Hideo</au><au>Korn, W.Michael</au><au>Lenz, Heinz-Josef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The impact of ARID1A mutation on molecular characteristics in colorectal cancer</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2020-11-01</date><risdate>2020</risdate><volume>140</volume><spage>119</spage><epage>129</epage><pages>119-129</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>ARID1A is a key subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex which regulates dynamic repositioning of nucleosomes to repair DNA damage. Only small pilot studies have evaluated the role of ARID1A mutation in colorectal cancer (CRC). The aim of the present study was to explore the potential impact of ARID1A mutation on clinicopathological and molecular characteristics in CRC.
We used integrated data sets of 7978 CRC cases (one data set from a clinical laboratory improvement amendments [CLIA]-certified laboratory and three independent published data sets). The associations of ARID1A mutation with molecular characteristics including immune profile (the status of microsatellite instability [MSI], tumour mutational burden [TMB], programmed death ligand 1 [PD-L1] and estimated infiltrating immune cells), clinicopathological features and related pathways were analysed using next-generation sequencing, RNA sequencing and immunohistochemistry.
ARID1A mutant samples had more genomically unstable tumour features (MSI-high and TMB-high) and exhibited more characteristics of a T-cell–inflamed microenvironment (PD-L1 expression and high estimated infiltrating cytotoxic T lymphocytes [CTLs]) than ARID1A wild-type samples in the discovery and validation cohorts. Even ARID1A mutant samples without MSI-high status were TMB-high, had high levels of PD-L1 expression and high estimated infiltrating CTLs. ARID1A mutations were more common with right-sided primary and earlier stage tumours. ARID1A mutant tumours mainly had co-occurring gene mutations related to chromatin modifying, DNA repair, WNT signalling and epidermal growth factor receptor inhibitor resistance pathways, and ARID1A mutations strongly regulated DNA repair pathways. Key genes for chemotherapy/radiotherapy sensitivity were suppressed in ARID1A mutant samples.
Our findings may provide novel insights to develop individualised approaches for treatment of CRC based on ARID1A mutation status.
•The impact of ARID1A mutations was analysed using 7978 colorectal cancer samples.•ARID1A mutation was linked to immune activation, right-sided tumour and early stage.•ARID1A mutation may be a biomarker for chemotherapy/radiotherapy and targeted therapy.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>33080474</pmid><doi>10.1016/j.ejca.2020.09.006</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2492-4043</orcidid><orcidid>https://orcid.org/0000-0003-0308-8223</orcidid><orcidid>https://orcid.org/0000-0002-6368-4177</orcidid><orcidid>https://orcid.org/0000-0002-9869-0163</orcidid><orcidid>https://orcid.org/0000-0002-9285-3849</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8009046 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adolescent Adult Aged Aged, 80 and over Apoptosis ARID1A Cancer Chemotherapy Chromatin Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - genetics Colorectal Neoplasms - immunology Cytotoxicity Data integration Datasets Deoxyribonucleic acid DNA DNA damage DNA repair DNA Repair - genetics DNA Repair - immunology DNA-Binding Proteins - genetics DNA-Binding Proteins - immunology Epidermal growth factor Female Gene sequencing Growth factors Humans Immune profile Immune system Immunohistochemistry Immunohistochemistry - methods Inflammation Laboratories Lymphocytes Lymphocytes T Male Microsatellite instability Middle Aged Molecular profile Mutants Mutation Mutation - genetics Mutation - immunology Next-generation sequencing Nucleosomes PD-L1 protein Radiation therapy Repair Resistance factors Ribonucleic acid Right-sided location RNA Signal transduction Sucrose Sugar SWI/SNF complex T-Lymphocytes, Cytotoxic - immunology Transcription Factors - genetics Transcription Factors - immunology Tumor Microenvironment - genetics Tumor Microenvironment - immunology Tumors Wnt protein Young Adult |
title | The impact of ARID1A mutation on molecular characteristics in colorectal cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T03%3A56%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20impact%20of%20ARID1A%20mutation%20on%20molecular%20characteristics%20in%20colorectal%20cancer&rft.jtitle=European%20journal%20of%20cancer%20(1990)&rft.au=Tokunaga,%20Ryuma&rft.date=2020-11-01&rft.volume=140&rft.spage=119&rft.epage=129&rft.pages=119-129&rft.issn=0959-8049&rft.eissn=1879-0852&rft_id=info:doi/10.1016/j.ejca.2020.09.006&rft_dat=%3Cproquest_pubme%3E2452982911%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2468390135&rft_id=info:pmid/33080474&rft_els_id=S0959804920304895&rfr_iscdi=true |