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Association of BRCA1, BRCA2, RAD51, and HER2 gene polymorphisms with the breast cancer risk in the Bangladeshi population

Purpose Breast cancer is considered as the most frequent female malignancy. Altered gene expressions due to genetic polymorphisms in the BRCA1, BRCA2, RAD51, and HER2 contribute toward the development of breast cancer, and yet, no such type of study has been conducted in the Bangladeshi population....

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Published in:Breast cancer (Tokyo, Japan) Japan), 2017-03, Vol.24 (2), p.229-237
Main Authors: Parvin, Salma, Islam, Md. Siddiqul, Al-Mamun, Mir Md. Abdullah, Islam, Mohammad Safiqul, Ahmed, Maizbha Uddin, Kabir, Eva Rahman, Hasnat, Abul
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container_title Breast cancer (Tokyo, Japan)
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creator Parvin, Salma
Islam, Md. Siddiqul
Al-Mamun, Mir Md. Abdullah
Islam, Mohammad Safiqul
Ahmed, Maizbha Uddin
Kabir, Eva Rahman
Hasnat, Abul
description Purpose Breast cancer is considered as the most frequent female malignancy. Altered gene expressions due to genetic polymorphisms in the BRCA1, BRCA2, RAD51, and HER2 contribute toward the development of breast cancer, and yet, no such type of study has been conducted in the Bangladeshi population. This study was designed to evaluate the role of BRCA1rs80357713, BRCA1rs80357906, BRCA2rs11571653, RAD51rs1801320, and HER2rs1136201 polymorphisms as risk factors in the development of breast cancer in the Bangladeshi population. Methods A total 310 patients with invasive breast cancers were recruited as cases from different public and private hospitals of Bangladesh, and 250 Bangladeshi healthy women matching age with the patients were recruited as controls. Polymerase chain reaction–restriction fragment length polymorphism method was used to analyze the genetic polymorphisms. Results Patients carrying BRCA1/2 mutations, GC and GC plus CC genotypes of RAD51rs1801320, and AG plus GG genotype of HER2rs1136201 polymorphisms were found to be associated with breast cancer. In subgroup analysis, AG plus GG genotype of HER2rs1136201 was found to be associated with the breast cancer risk in the patients younger than 45 years of age compared with the older patients having more than 45 years of age, and RAD51rs1801320 was related to the tumor size and tumor aggressiveness (higher graded tumor). Conclusion Our results indicate that BRCA1/BRCA2, RAD51rs1801320 and HER2rs1136201 polymorphisms were associated with breast cancer in the studied population.
doi_str_mv 10.1007/s12282-016-0692-5
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Siddiqul ; Al-Mamun, Mir Md. Abdullah ; Islam, Mohammad Safiqul ; Ahmed, Maizbha Uddin ; Kabir, Eva Rahman ; Hasnat, Abul</creator><creatorcontrib>Parvin, Salma ; Islam, Md. Siddiqul ; Al-Mamun, Mir Md. Abdullah ; Islam, Mohammad Safiqul ; Ahmed, Maizbha Uddin ; Kabir, Eva Rahman ; Hasnat, Abul</creatorcontrib><description>Purpose Breast cancer is considered as the most frequent female malignancy. Altered gene expressions due to genetic polymorphisms in the BRCA1, BRCA2, RAD51, and HER2 contribute toward the development of breast cancer, and yet, no such type of study has been conducted in the Bangladeshi population. This study was designed to evaluate the role of BRCA1rs80357713, BRCA1rs80357906, BRCA2rs11571653, RAD51rs1801320, and HER2rs1136201 polymorphisms as risk factors in the development of breast cancer in the Bangladeshi population. Methods A total 310 patients with invasive breast cancers were recruited as cases from different public and private hospitals of Bangladesh, and 250 Bangladeshi healthy women matching age with the patients were recruited as controls. Polymerase chain reaction–restriction fragment length polymorphism method was used to analyze the genetic polymorphisms. Results Patients carrying BRCA1/2 mutations, GC and GC plus CC genotypes of RAD51rs1801320, and AG plus GG genotype of HER2rs1136201 polymorphisms were found to be associated with breast cancer. In subgroup analysis, AG plus GG genotype of HER2rs1136201 was found to be associated with the breast cancer risk in the patients younger than 45 years of age compared with the older patients having more than 45 years of age, and RAD51rs1801320 was related to the tumor size and tumor aggressiveness (higher graded tumor). Conclusion Our results indicate that BRCA1/BRCA2, RAD51rs1801320 and HER2rs1136201 polymorphisms were associated with breast cancer in the studied population.</description><identifier>ISSN: 1340-6868</identifier><identifier>EISSN: 1880-4233</identifier><identifier>DOI: 10.1007/s12282-016-0692-5</identifier><identifier>PMID: 27068824</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Adult ; Bangladesh ; BRCA1 Protein - genetics ; BRCA2 Protein - genetics ; Breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Cancer ; Cancer Research ; Case-Control Studies ; Development and progression ; Female ; Gene expression ; Genes ; Genetic aspects ; Genetic polymorphisms ; Genetic Predisposition to Disease ; Genetic research ; Genetics, Population ; Health aspects ; Humans ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Mutation ; Oncology ; Oncology, Experimental ; Original Article ; Polymorphism, Single Nucleotide ; Rad51 Recombinase - genetics ; Receptor, ErbB-2 - genetics ; Risk factors ; Surgery ; Surgical Oncology ; Women</subject><ispartof>Breast cancer (Tokyo, Japan), 2017-03, Vol.24 (2), p.229-237</ispartof><rights>The Japanese Breast Cancer Society 2016</rights><rights>COPYRIGHT 2017 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-6b3cf2e14e365c0aa413ec207be7aa226e29a8f2eeb3ec441bb6e154e2d3b32b3</citedby><cites>FETCH-LOGICAL-c435t-6b3cf2e14e365c0aa413ec207be7aa226e29a8f2eeb3ec441bb6e154e2d3b32b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27068824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parvin, Salma</creatorcontrib><creatorcontrib>Islam, Md. Siddiqul</creatorcontrib><creatorcontrib>Al-Mamun, Mir Md. Abdullah</creatorcontrib><creatorcontrib>Islam, Mohammad Safiqul</creatorcontrib><creatorcontrib>Ahmed, Maizbha Uddin</creatorcontrib><creatorcontrib>Kabir, Eva Rahman</creatorcontrib><creatorcontrib>Hasnat, Abul</creatorcontrib><title>Association of BRCA1, BRCA2, RAD51, and HER2 gene polymorphisms with the breast cancer risk in the Bangladeshi population</title><title>Breast cancer (Tokyo, Japan)</title><addtitle>Breast Cancer</addtitle><addtitle>Breast Cancer</addtitle><description>Purpose Breast cancer is considered as the most frequent female malignancy. Altered gene expressions due to genetic polymorphisms in the BRCA1, BRCA2, RAD51, and HER2 contribute toward the development of breast cancer, and yet, no such type of study has been conducted in the Bangladeshi population. This study was designed to evaluate the role of BRCA1rs80357713, BRCA1rs80357906, BRCA2rs11571653, RAD51rs1801320, and HER2rs1136201 polymorphisms as risk factors in the development of breast cancer in the Bangladeshi population. Methods A total 310 patients with invasive breast cancers were recruited as cases from different public and private hospitals of Bangladesh, and 250 Bangladeshi healthy women matching age with the patients were recruited as controls. Polymerase chain reaction–restriction fragment length polymorphism method was used to analyze the genetic polymorphisms. Results Patients carrying BRCA1/2 mutations, GC and GC plus CC genotypes of RAD51rs1801320, and AG plus GG genotype of HER2rs1136201 polymorphisms were found to be associated with breast cancer. In subgroup analysis, AG plus GG genotype of HER2rs1136201 was found to be associated with the breast cancer risk in the patients younger than 45 years of age compared with the older patients having more than 45 years of age, and RAD51rs1801320 was related to the tumor size and tumor aggressiveness (higher graded tumor). Conclusion Our results indicate that BRCA1/BRCA2, RAD51rs1801320 and HER2rs1136201 polymorphisms were associated with breast cancer in the studied population.</description><subject>Adult</subject><subject>Bangladesh</subject><subject>BRCA1 Protein - genetics</subject><subject>BRCA2 Protein - genetics</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Case-Control Studies</subject><subject>Development and progression</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic polymorphisms</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetic research</subject><subject>Genetics, Population</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Oncology</subject><subject>Oncology, Experimental</subject><subject>Original Article</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Rad51 Recombinase - genetics</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>Risk factors</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Women</subject><issn>1340-6868</issn><issn>1880-4233</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kV2L1TAQhoMo7of-AG8k4I0X2zVfTbOX3eN-CAvCQa9Dmk7PydomNWmR8-9NT3cFQSQXk5l53kmYF6F3lFxSQqpPiTKmWEGoLIi8YkX5Ap1SpUghGOcv850LUkgl1Qk6S-mREMErIl-jE5aDUkycokOdUrDOTC54HDp8vd3U9OIY2AXe1p_LnBnf4vubLcM78IDH0B-GEMe9S0PCv9y0x9MecBPBpAlb4y1EHF36gZ0_dq6N3_WmhbR3WTzO_fG1N-hVZ_oEb5_iOfp-e_Ntc188fL37sqkfCit4ORWy4bZjQAVwWVpijKAcLCNVA5UxjElgV0ZlAppcF4I2jQRaCmAtbzhr-Dn6uM4dY_g5Q5r04JKFvjcewpw0VUxKqQivMvphRXemB-18F6Zo7ILrulp2nTdYZuryH1Q-LQzOBg-dy_W_BHQV2BhSitDpMbrBxIOmRC9G6tVInY3Ui5F60bx_-vXcDND-UTw7lwG2Aim3_A6ifgxz9HmT_5n6GwwppbM</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Parvin, Salma</creator><creator>Islam, Md. 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Abdullah ; Islam, Mohammad Safiqul ; Ahmed, Maizbha Uddin ; Kabir, Eva Rahman ; Hasnat, Abul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-6b3cf2e14e365c0aa413ec207be7aa226e29a8f2eeb3ec441bb6e154e2d3b32b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Bangladesh</topic><topic>BRCA1 Protein - genetics</topic><topic>BRCA2 Protein - genetics</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Case-Control Studies</topic><topic>Development and progression</topic><topic>Female</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic polymorphisms</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetic research</topic><topic>Genetics, Population</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Oncology</topic><topic>Oncology, Experimental</topic><topic>Original Article</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Rad51 Recombinase - genetics</topic><topic>Receptor, ErbB-2 - genetics</topic><topic>Risk factors</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parvin, Salma</creatorcontrib><creatorcontrib>Islam, Md. Siddiqul</creatorcontrib><creatorcontrib>Al-Mamun, Mir Md. Abdullah</creatorcontrib><creatorcontrib>Islam, Mohammad Safiqul</creatorcontrib><creatorcontrib>Ahmed, Maizbha Uddin</creatorcontrib><creatorcontrib>Kabir, Eva Rahman</creatorcontrib><creatorcontrib>Hasnat, Abul</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Breast cancer (Tokyo, Japan)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parvin, Salma</au><au>Islam, Md. Siddiqul</au><au>Al-Mamun, Mir Md. Abdullah</au><au>Islam, Mohammad Safiqul</au><au>Ahmed, Maizbha Uddin</au><au>Kabir, Eva Rahman</au><au>Hasnat, Abul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of BRCA1, BRCA2, RAD51, and HER2 gene polymorphisms with the breast cancer risk in the Bangladeshi population</atitle><jtitle>Breast cancer (Tokyo, Japan)</jtitle><stitle>Breast Cancer</stitle><addtitle>Breast Cancer</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>24</volume><issue>2</issue><spage>229</spage><epage>237</epage><pages>229-237</pages><issn>1340-6868</issn><eissn>1880-4233</eissn><abstract>Purpose Breast cancer is considered as the most frequent female malignancy. Altered gene expressions due to genetic polymorphisms in the BRCA1, BRCA2, RAD51, and HER2 contribute toward the development of breast cancer, and yet, no such type of study has been conducted in the Bangladeshi population. This study was designed to evaluate the role of BRCA1rs80357713, BRCA1rs80357906, BRCA2rs11571653, RAD51rs1801320, and HER2rs1136201 polymorphisms as risk factors in the development of breast cancer in the Bangladeshi population. Methods A total 310 patients with invasive breast cancers were recruited as cases from different public and private hospitals of Bangladesh, and 250 Bangladeshi healthy women matching age with the patients were recruited as controls. Polymerase chain reaction–restriction fragment length polymorphism method was used to analyze the genetic polymorphisms. Results Patients carrying BRCA1/2 mutations, GC and GC plus CC genotypes of RAD51rs1801320, and AG plus GG genotype of HER2rs1136201 polymorphisms were found to be associated with breast cancer. In subgroup analysis, AG plus GG genotype of HER2rs1136201 was found to be associated with the breast cancer risk in the patients younger than 45 years of age compared with the older patients having more than 45 years of age, and RAD51rs1801320 was related to the tumor size and tumor aggressiveness (higher graded tumor). Conclusion Our results indicate that BRCA1/BRCA2, RAD51rs1801320 and HER2rs1136201 polymorphisms were associated with breast cancer in the studied population.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>27068824</pmid><doi>10.1007/s12282-016-0692-5</doi><tpages>9</tpages></addata></record>
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identifier ISSN: 1340-6868
ispartof Breast cancer (Tokyo, Japan), 2017-03, Vol.24 (2), p.229-237
issn 1340-6868
1880-4233
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source Springer Nature
subjects Adult
Bangladesh
BRCA1 Protein - genetics
BRCA2 Protein - genetics
Breast cancer
Breast Neoplasms - genetics
Breast Neoplasms - pathology
Cancer
Cancer Research
Case-Control Studies
Development and progression
Female
Gene expression
Genes
Genetic aspects
Genetic polymorphisms
Genetic Predisposition to Disease
Genetic research
Genetics, Population
Health aspects
Humans
Medicine
Medicine & Public Health
Middle Aged
Mutation
Oncology
Oncology, Experimental
Original Article
Polymorphism, Single Nucleotide
Rad51 Recombinase - genetics
Receptor, ErbB-2 - genetics
Risk factors
Surgery
Surgical Oncology
Women
title Association of BRCA1, BRCA2, RAD51, and HER2 gene polymorphisms with the breast cancer risk in the Bangladeshi population
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