Germline APOBEC3B deletion is associated with breast cancer risk in an Asian multi-ethnic cohort and with immune cell presentation

APOBEC3B is a cytosine deaminase implicated in immune response to viral infection, cancer predisposition and carcinogenesis. Germline APOBEC3B deletion is more common in East Asian women and confers a modest risk to breast cancer in both East Asian and Caucasian women. Analysis of tumour samples fro...

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Veröffentlicht in:Breast cancer research : BCR 2016-05, Vol.18 (1), p.56, Article 56
Hauptverfasser: Wen, Wei Xiong, Soo, Jaslyn Sian-Siu, Kwan, Pui Yoke, Hong, Elaine, Khang, Tsung Fei, Mariapun, Shivaani, Lee, Christine Shu-Mei, Hasan, Siti Norhidayu, Rajadurai, Pathmanathan, Yip, Cheng Har, Mohd Taib, Nur Aishah, Teo, Soo Hwang
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container_issue 1
container_start_page 56
container_title Breast cancer research : BCR
container_volume 18
creator Wen, Wei Xiong
Soo, Jaslyn Sian-Siu
Kwan, Pui Yoke
Hong, Elaine
Khang, Tsung Fei
Mariapun, Shivaani
Lee, Christine Shu-Mei
Hasan, Siti Norhidayu
Rajadurai, Pathmanathan
Yip, Cheng Har
Mohd Taib, Nur Aishah
Teo, Soo Hwang
description APOBEC3B is a cytosine deaminase implicated in immune response to viral infection, cancer predisposition and carcinogenesis. Germline APOBEC3B deletion is more common in East Asian women and confers a modest risk to breast cancer in both East Asian and Caucasian women. Analysis of tumour samples from women of European descent has shown that germline APOBEC3B deletion is associated with an increased propensity to develop somatic mutations and with an enrichment for immune response-related gene sets. However, this has not been examined in Asian tumour samples, where population differences in genetic and dietary factors may have an impact on the immune system. In this study, we determined the prevalence of germline APOBEC3B deletion and its association with breast cancer risk in a cross-sectional hospital-based Asian multi-ethnic cohort of 1451 cases and 1442 controls from Malaysia. We compared gene expression profiles of breast cancers arising from APOBEC3B deletion carriers and non-carriers using microarray analyses. Finally, we characterised the overall abundance of tumour-infiltrating immune cells in breast cancers from TCGA and METABRIC using ESTIMATE and relative frequency of 22 immune cell subsets in breast cancers from METABRIC using CIBERSORT. The minor allelic frequency of APOBEC3B deletion was estimated to be 0.35, 0.42 and 0.16 in female populations of Chinese, Malay and Indian descent, respectively, and that germline APOBEC3B deletion was associated with breast cancer risk with odds ratios of 1.23 (95 % CI: [1.05, 1.44]) for one-copy deletion and 1.38 (95 % CI: [1.10, 1.74]) for two-copy deletion compared to women with no deletion. Germline APOBEC3B deletion was not associated with any clinicopathologic features or the expression of any APOBEC family members but was associated with immune response-related gene sets (FDR q values 
doi_str_mv 10.1186/s13058-016-0717-1
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Germline APOBEC3B deletion is more common in East Asian women and confers a modest risk to breast cancer in both East Asian and Caucasian women. Analysis of tumour samples from women of European descent has shown that germline APOBEC3B deletion is associated with an increased propensity to develop somatic mutations and with an enrichment for immune response-related gene sets. However, this has not been examined in Asian tumour samples, where population differences in genetic and dietary factors may have an impact on the immune system. In this study, we determined the prevalence of germline APOBEC3B deletion and its association with breast cancer risk in a cross-sectional hospital-based Asian multi-ethnic cohort of 1451 cases and 1442 controls from Malaysia. We compared gene expression profiles of breast cancers arising from APOBEC3B deletion carriers and non-carriers using microarray analyses. Finally, we characterised the overall abundance of tumour-infiltrating immune cells in breast cancers from TCGA and METABRIC using ESTIMATE and relative frequency of 22 immune cell subsets in breast cancers from METABRIC using CIBERSORT. The minor allelic frequency of APOBEC3B deletion was estimated to be 0.35, 0.42 and 0.16 in female populations of Chinese, Malay and Indian descent, respectively, and that germline APOBEC3B deletion was associated with breast cancer risk with odds ratios of 1.23 (95 % CI: [1.05, 1.44]) for one-copy deletion and 1.38 (95 % CI: [1.10, 1.74]) for two-copy deletion compared to women with no deletion. Germline APOBEC3B deletion was not associated with any clinicopathologic features or the expression of any APOBEC family members but was associated with immune response-related gene sets (FDR q values &lt; 0.05). Analysis of breast cancers from METABRIC revealed breast cancers from APOBEC3B deletion carriers to have significantly higher abundance of tumour-infiltrating immune cells (P &lt; 0.001). Taken together, our data suggests that tumour-infiltrating immune cells may be an important feature of breast cancers arising in women with APOBEC3B germline deletion, and that this may be of particular interest in Asian women where the germline deletion is more common.</description><identifier>ISSN: 1465-542X</identifier><identifier>ISSN: 1465-5411</identifier><identifier>EISSN: 1465-542X</identifier><identifier>DOI: 10.1186/s13058-016-0717-1</identifier><identifier>PMID: 27233495</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Analysis ; Antigen Presentation ; Apolipoproteins ; Breast cancer ; Breast Neoplasms - epidemiology ; Breast Neoplasms - genetics ; Breast Neoplasms - immunology ; Breast Neoplasms - pathology ; Carcinogenesis ; Case-Control Studies ; Cross-Sectional Studies ; Cytidine Deaminase - genetics ; DNA Copy Number Variations ; DNA microarrays ; Ethnic Groups - genetics ; Female ; Gene Expression ; Gene Expression Profiling ; Genetic aspects ; Genetic Predisposition to Disease ; Germ-Line Mutation ; Health aspects ; Heterozygote ; Humans ; Immunity - genetics ; Influence ; Lymphocytes, Tumor-Infiltrating - immunology ; Lymphocytes, Tumor-Infiltrating - metabolism ; Malaysia - epidemiology ; Malaysia - ethnology ; Middle Aged ; Minor Histocompatibility Antigens - genetics ; Protein Isoforms ; Risk ; Risk factors ; Sequence Deletion</subject><ispartof>Breast cancer research : BCR, 2016-05, Vol.18 (1), p.56, Article 56</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-10e8f73da2dd998481699b744769014525c69311a56f0ba7dc9231fb4905f6fd3</citedby><cites>FETCH-LOGICAL-c466t-10e8f73da2dd998481699b744769014525c69311a56f0ba7dc9231fb4905f6fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884363/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884363/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27233495$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wen, Wei Xiong</creatorcontrib><creatorcontrib>Soo, Jaslyn Sian-Siu</creatorcontrib><creatorcontrib>Kwan, Pui Yoke</creatorcontrib><creatorcontrib>Hong, Elaine</creatorcontrib><creatorcontrib>Khang, Tsung Fei</creatorcontrib><creatorcontrib>Mariapun, Shivaani</creatorcontrib><creatorcontrib>Lee, Christine Shu-Mei</creatorcontrib><creatorcontrib>Hasan, Siti Norhidayu</creatorcontrib><creatorcontrib>Rajadurai, Pathmanathan</creatorcontrib><creatorcontrib>Yip, Cheng Har</creatorcontrib><creatorcontrib>Mohd Taib, Nur Aishah</creatorcontrib><creatorcontrib>Teo, Soo Hwang</creatorcontrib><title>Germline APOBEC3B deletion is associated with breast cancer risk in an Asian multi-ethnic cohort and with immune cell presentation</title><title>Breast cancer research : BCR</title><addtitle>Breast Cancer Res</addtitle><description>APOBEC3B is a cytosine deaminase implicated in immune response to viral infection, cancer predisposition and carcinogenesis. Germline APOBEC3B deletion is more common in East Asian women and confers a modest risk to breast cancer in both East Asian and Caucasian women. Analysis of tumour samples from women of European descent has shown that germline APOBEC3B deletion is associated with an increased propensity to develop somatic mutations and with an enrichment for immune response-related gene sets. However, this has not been examined in Asian tumour samples, where population differences in genetic and dietary factors may have an impact on the immune system. In this study, we determined the prevalence of germline APOBEC3B deletion and its association with breast cancer risk in a cross-sectional hospital-based Asian multi-ethnic cohort of 1451 cases and 1442 controls from Malaysia. We compared gene expression profiles of breast cancers arising from APOBEC3B deletion carriers and non-carriers using microarray analyses. Finally, we characterised the overall abundance of tumour-infiltrating immune cells in breast cancers from TCGA and METABRIC using ESTIMATE and relative frequency of 22 immune cell subsets in breast cancers from METABRIC using CIBERSORT. The minor allelic frequency of APOBEC3B deletion was estimated to be 0.35, 0.42 and 0.16 in female populations of Chinese, Malay and Indian descent, respectively, and that germline APOBEC3B deletion was associated with breast cancer risk with odds ratios of 1.23 (95 % CI: [1.05, 1.44]) for one-copy deletion and 1.38 (95 % CI: [1.10, 1.74]) for two-copy deletion compared to women with no deletion. Germline APOBEC3B deletion was not associated with any clinicopathologic features or the expression of any APOBEC family members but was associated with immune response-related gene sets (FDR q values &lt; 0.05). Analysis of breast cancers from METABRIC revealed breast cancers from APOBEC3B deletion carriers to have significantly higher abundance of tumour-infiltrating immune cells (P &lt; 0.001). Taken together, our data suggests that tumour-infiltrating immune cells may be an important feature of breast cancers arising in women with APOBEC3B germline deletion, and that this may be of particular interest in Asian women where the germline deletion is more common.</description><subject>Adult</subject><subject>Analysis</subject><subject>Antigen Presentation</subject><subject>Apolipoproteins</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - epidemiology</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - immunology</subject><subject>Breast Neoplasms - pathology</subject><subject>Carcinogenesis</subject><subject>Case-Control Studies</subject><subject>Cross-Sectional Studies</subject><subject>Cytidine Deaminase - genetics</subject><subject>DNA Copy Number Variations</subject><subject>DNA microarrays</subject><subject>Ethnic Groups - genetics</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Genetic aspects</subject><subject>Genetic Predisposition to Disease</subject><subject>Germ-Line Mutation</subject><subject>Health aspects</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Immunity - genetics</subject><subject>Influence</subject><subject>Lymphocytes, Tumor-Infiltrating - immunology</subject><subject>Lymphocytes, Tumor-Infiltrating - metabolism</subject><subject>Malaysia - epidemiology</subject><subject>Malaysia - ethnology</subject><subject>Middle Aged</subject><subject>Minor Histocompatibility Antigens - genetics</subject><subject>Protein Isoforms</subject><subject>Risk</subject><subject>Risk factors</subject><subject>Sequence Deletion</subject><issn>1465-542X</issn><issn>1465-5411</issn><issn>1465-542X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptUVtrFDEUDqLYi_4AXyTg89ScyWWSF2G7tFUo1AcF30Iml250JlmS2Yqv_nKzbi0tSODkkPNdcvgQegPkDECK9xUo4bIjIDoywNDBM3QMTPCOs_7b80f9ETqp9TshMEguX6KjfugpZYofo99XvsxTTB6vPt-cX6zpOXZ-8kvMCceKTa3ZRrN4h3_GZYPH4k1dsDXJ-oJLrD9wTNgkvKqx1Xk3LbHzyyZFi23e5LK04T03zvOu-Vg_TXhbfPVpMXufV-hFMFP1r-_vU_T18uLL-mN3fXP1ab267iwTYumAeBkG6kzvnFKSSRBKjQNjg1AEGO-5FYoCGC4CGc3grOophJEpwoMIjp6iDwfd7W6cvbPNv5hJb0ucTfmls4n66STFjb7Nd5pJyaigTeDdQeDWTF7HFHKD2TlWq1eMU8G5-os6-w-qHefnaHPyIbb3JwQ4EGzJtRYfHr4ERO9z1oecdctZ73PW0DhvH-_ywPgXLP0DWe2kQA</recordid><startdate>20160527</startdate><enddate>20160527</enddate><creator>Wen, Wei Xiong</creator><creator>Soo, Jaslyn Sian-Siu</creator><creator>Kwan, Pui Yoke</creator><creator>Hong, Elaine</creator><creator>Khang, Tsung Fei</creator><creator>Mariapun, Shivaani</creator><creator>Lee, Christine Shu-Mei</creator><creator>Hasan, Siti Norhidayu</creator><creator>Rajadurai, Pathmanathan</creator><creator>Yip, Cheng Har</creator><creator>Mohd Taib, Nur Aishah</creator><creator>Teo, Soo Hwang</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>5PM</scope></search><sort><creationdate>20160527</creationdate><title>Germline APOBEC3B deletion is associated with breast cancer risk in an Asian multi-ethnic cohort and with immune cell presentation</title><author>Wen, Wei Xiong ; Soo, Jaslyn Sian-Siu ; Kwan, Pui Yoke ; Hong, Elaine ; Khang, Tsung Fei ; Mariapun, Shivaani ; Lee, Christine Shu-Mei ; Hasan, Siti Norhidayu ; Rajadurai, Pathmanathan ; Yip, Cheng Har ; Mohd Taib, Nur Aishah ; Teo, Soo Hwang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-10e8f73da2dd998481699b744769014525c69311a56f0ba7dc9231fb4905f6fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Analysis</topic><topic>Antigen Presentation</topic><topic>Apolipoproteins</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - epidemiology</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - immunology</topic><topic>Breast Neoplasms - pathology</topic><topic>Carcinogenesis</topic><topic>Case-Control Studies</topic><topic>Cross-Sectional Studies</topic><topic>Cytidine Deaminase - genetics</topic><topic>DNA Copy Number Variations</topic><topic>DNA microarrays</topic><topic>Ethnic Groups - genetics</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Gene Expression Profiling</topic><topic>Genetic aspects</topic><topic>Genetic Predisposition to Disease</topic><topic>Germ-Line Mutation</topic><topic>Health aspects</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Immunity - genetics</topic><topic>Influence</topic><topic>Lymphocytes, Tumor-Infiltrating - immunology</topic><topic>Lymphocytes, Tumor-Infiltrating - metabolism</topic><topic>Malaysia - epidemiology</topic><topic>Malaysia - ethnology</topic><topic>Middle Aged</topic><topic>Minor Histocompatibility Antigens - genetics</topic><topic>Protein Isoforms</topic><topic>Risk</topic><topic>Risk factors</topic><topic>Sequence Deletion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wen, Wei Xiong</creatorcontrib><creatorcontrib>Soo, Jaslyn Sian-Siu</creatorcontrib><creatorcontrib>Kwan, Pui Yoke</creatorcontrib><creatorcontrib>Hong, Elaine</creatorcontrib><creatorcontrib>Khang, Tsung Fei</creatorcontrib><creatorcontrib>Mariapun, Shivaani</creatorcontrib><creatorcontrib>Lee, Christine Shu-Mei</creatorcontrib><creatorcontrib>Hasan, Siti Norhidayu</creatorcontrib><creatorcontrib>Rajadurai, Pathmanathan</creatorcontrib><creatorcontrib>Yip, Cheng Har</creatorcontrib><creatorcontrib>Mohd Taib, Nur Aishah</creatorcontrib><creatorcontrib>Teo, Soo Hwang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Breast cancer research : BCR</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wen, Wei Xiong</au><au>Soo, Jaslyn Sian-Siu</au><au>Kwan, Pui Yoke</au><au>Hong, Elaine</au><au>Khang, Tsung Fei</au><au>Mariapun, Shivaani</au><au>Lee, Christine Shu-Mei</au><au>Hasan, Siti Norhidayu</au><au>Rajadurai, Pathmanathan</au><au>Yip, Cheng Har</au><au>Mohd Taib, Nur Aishah</au><au>Teo, Soo Hwang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Germline APOBEC3B deletion is associated with breast cancer risk in an Asian multi-ethnic cohort and with immune cell presentation</atitle><jtitle>Breast cancer research : BCR</jtitle><addtitle>Breast Cancer Res</addtitle><date>2016-05-27</date><risdate>2016</risdate><volume>18</volume><issue>1</issue><spage>56</spage><pages>56-</pages><artnum>56</artnum><issn>1465-542X</issn><issn>1465-5411</issn><eissn>1465-542X</eissn><abstract>APOBEC3B is a cytosine deaminase implicated in immune response to viral infection, cancer predisposition and carcinogenesis. Germline APOBEC3B deletion is more common in East Asian women and confers a modest risk to breast cancer in both East Asian and Caucasian women. Analysis of tumour samples from women of European descent has shown that germline APOBEC3B deletion is associated with an increased propensity to develop somatic mutations and with an enrichment for immune response-related gene sets. However, this has not been examined in Asian tumour samples, where population differences in genetic and dietary factors may have an impact on the immune system. In this study, we determined the prevalence of germline APOBEC3B deletion and its association with breast cancer risk in a cross-sectional hospital-based Asian multi-ethnic cohort of 1451 cases and 1442 controls from Malaysia. We compared gene expression profiles of breast cancers arising from APOBEC3B deletion carriers and non-carriers using microarray analyses. Finally, we characterised the overall abundance of tumour-infiltrating immune cells in breast cancers from TCGA and METABRIC using ESTIMATE and relative frequency of 22 immune cell subsets in breast cancers from METABRIC using CIBERSORT. The minor allelic frequency of APOBEC3B deletion was estimated to be 0.35, 0.42 and 0.16 in female populations of Chinese, Malay and Indian descent, respectively, and that germline APOBEC3B deletion was associated with breast cancer risk with odds ratios of 1.23 (95 % CI: [1.05, 1.44]) for one-copy deletion and 1.38 (95 % CI: [1.10, 1.74]) for two-copy deletion compared to women with no deletion. Germline APOBEC3B deletion was not associated with any clinicopathologic features or the expression of any APOBEC family members but was associated with immune response-related gene sets (FDR q values &lt; 0.05). Analysis of breast cancers from METABRIC revealed breast cancers from APOBEC3B deletion carriers to have significantly higher abundance of tumour-infiltrating immune cells (P &lt; 0.001). Taken together, our data suggests that tumour-infiltrating immune cells may be an important feature of breast cancers arising in women with APOBEC3B germline deletion, and that this may be of particular interest in Asian women where the germline deletion is more common.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27233495</pmid><doi>10.1186/s13058-016-0717-1</doi><oa>free_for_read</oa></addata></record>
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subjects Adult
Analysis
Antigen Presentation
Apolipoproteins
Breast cancer
Breast Neoplasms - epidemiology
Breast Neoplasms - genetics
Breast Neoplasms - immunology
Breast Neoplasms - pathology
Carcinogenesis
Case-Control Studies
Cross-Sectional Studies
Cytidine Deaminase - genetics
DNA Copy Number Variations
DNA microarrays
Ethnic Groups - genetics
Female
Gene Expression
Gene Expression Profiling
Genetic aspects
Genetic Predisposition to Disease
Germ-Line Mutation
Health aspects
Heterozygote
Humans
Immunity - genetics
Influence
Lymphocytes, Tumor-Infiltrating - immunology
Lymphocytes, Tumor-Infiltrating - metabolism
Malaysia - epidemiology
Malaysia - ethnology
Middle Aged
Minor Histocompatibility Antigens - genetics
Protein Isoforms
Risk
Risk factors
Sequence Deletion
title Germline APOBEC3B deletion is associated with breast cancer risk in an Asian multi-ethnic cohort and with immune cell presentation
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