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...
Gespeichert in:
Veröffentlicht in: | Breast cancer research : BCR 2016-05, Vol.18 (1), p.56, Article 56 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
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 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4884363</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A453655963</galeid><sourcerecordid>A453655963</sourcerecordid><originalsourceid>FETCH-LOGICAL-c466t-10e8f73da2dd998481699b744769014525c69311a56f0ba7dc9231fb4905f6fd3</originalsourceid><addsrcrecordid>eNptUVtrFDEUDqLYi_4AXyTg89ScyWWSF2G7tFUo1AcF30Iml250JlmS2Yqv_nKzbi0tSODkkPNdcvgQegPkDECK9xUo4bIjIDoywNDBM3QMTPCOs_7b80f9ETqp9TshMEguX6KjfugpZYofo99XvsxTTB6vPt-cX6zpOXZ-8kvMCceKTa3ZRrN4h3_GZYPH4k1dsDXJ-oJLrD9wTNgkvKqx1Xk3LbHzyyZFi23e5LK04T03zvOu-Vg_TXhbfPVpMXufV-hFMFP1r-_vU_T18uLL-mN3fXP1ab267iwTYumAeBkG6kzvnFKSSRBKjQNjg1AEGO-5FYoCGC4CGc3grOophJEpwoMIjp6iDwfd7W6cvbPNv5hJb0ucTfmls4n66STFjb7Nd5pJyaigTeDdQeDWTF7HFHKD2TlWq1eMU8G5-os6-w-qHefnaHPyIbb3JwQ4EGzJtRYfHr4ERO9z1oecdctZ73PW0DhvH-_ywPgXLP0DWe2kQA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Germline APOBEC3B deletion is associated with breast cancer risk in an Asian multi-ethnic cohort and with immune cell presentation</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>SpringerNature Journals</source><source>PubMed Central Open Access</source><source>Springer Nature OA Free Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><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</creator><creatorcontrib>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</creatorcontrib><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 < 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 < 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 < 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 < 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 < 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 < 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> |
fulltext | fulltext |
identifier | ISSN: 1465-542X |
ispartof | Breast cancer research : BCR, 2016-05, Vol.18 (1), p.56, Article 56 |
issn | 1465-542X 1465-5411 1465-542X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4884363 |
source | MEDLINE; DOAJ Directory of Open Access Journals; SpringerNature Journals; PubMed Central Open Access; Springer Nature OA Free Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T17%3A09%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Germline%20APOBEC3B%20deletion%20is%20associated%20with%20breast%20cancer%20risk%20in%20an%20Asian%20multi-ethnic%20cohort%20and%20with%20immune%20cell%20presentation&rft.jtitle=Breast%20cancer%20research%20:%20BCR&rft.au=Wen,%20Wei%20Xiong&rft.date=2016-05-27&rft.volume=18&rft.issue=1&rft.spage=56&rft.pages=56-&rft.artnum=56&rft.issn=1465-542X&rft.eissn=1465-542X&rft_id=info:doi/10.1186/s13058-016-0717-1&rft_dat=%3Cgale_pubme%3EA453655963%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/27233495&rft_galeid=A453655963&rfr_iscdi=true |