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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Veröffentlicht in:European journal of cancer (1990) 2020-11, Vol.140, p.119-129
Hauptverfasser: 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
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container_issue
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container_title European journal of cancer (1990)
container_volume 140
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
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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. 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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 ; 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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. 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identifier ISSN: 0959-8049
ispartof European journal of cancer (1990), 2020-11, Vol.140, p.119-129
issn 0959-8049
1879-0852
language eng
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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
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