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Association between LAPTM4B gene polymorphism and breast cancer susceptibility in an Iranian population
Lysosome associated protein transmembrane 4beta (LAPTM4B) contribute to the risk of numerous cancers. The present study focused on the possible association between LAPTM4B polymorphism and the risk of breast cancer (BC) in an Iranian population in southeast Iran. This case control study includes 311...
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Published in: | Medical oncology (Northwood, London, England) London, England), 2014-08, Vol.31 (8), p.111-111, Article 111 |
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container_end_page | 111 |
container_issue | 8 |
container_start_page | 111 |
container_title | Medical oncology (Northwood, London, England) |
container_volume | 31 |
creator | Hashemi, Mohammad Amininia, Sahadi Ebrahimi, Mahboubeh Hashemi, Seyed Mehdi Yousefi, Javad Eskandari-Nasab, Ebrahim Taheri, Mohsen Ghavami, Saeid |
description | Lysosome associated protein transmembrane 4beta (LAPTM4B) contribute to the risk of numerous cancers. The present study focused on the possible association between
LAPTM4B
polymorphism and the risk of breast cancer (BC) in an Iranian population in southeast Iran. This case control study includes 311 BC patients and 225 healthy women. Genomic DNA was extracted from the whole blood by salting out method and
LAPTM4B
genotype was investigated using polymerase chain reaction. Our findings showed that
LAPTM4B
genotype was not associated with the risk of BC in any inheritance model tested. The minor allele frequency in case and control group was 0.297 and 0.278, respectively. The minor allele (LAPTM4B*2) was not associated with BC risk in comparison with
LAPTM4B*1
allele (odds ratio 1.10, 95 % confidence intervals 0.84–1.44,
p
= 0.495). Moreover,
LAPTM4B
polymorphism was not associated with clinical and pathological characteristics in the patient group. In conclusion, the findings of our study suggested that the polymorphism of
LAPTM4B
gene was not associated with susceptibility to BC and clinicopathological characteristics in an Iranian population. |
doi_str_mv | 10.1007/s12032-014-0111-8 |
format | article |
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LAPTM4B
polymorphism and the risk of breast cancer (BC) in an Iranian population in southeast Iran. This case control study includes 311 BC patients and 225 healthy women. Genomic DNA was extracted from the whole blood by salting out method and
LAPTM4B
genotype was investigated using polymerase chain reaction. Our findings showed that
LAPTM4B
genotype was not associated with the risk of BC in any inheritance model tested. The minor allele frequency in case and control group was 0.297 and 0.278, respectively. The minor allele (LAPTM4B*2) was not associated with BC risk in comparison with
LAPTM4B*1
allele (odds ratio 1.10, 95 % confidence intervals 0.84–1.44,
p
= 0.495). Moreover,
LAPTM4B
polymorphism was not associated with clinical and pathological characteristics in the patient group. In conclusion, the findings of our study suggested that the polymorphism of
LAPTM4B
gene was not associated with susceptibility to BC and clinicopathological characteristics in an Iranian population.</description><identifier>ISSN: 1357-0560</identifier><identifier>EISSN: 1559-131X</identifier><identifier>DOI: 10.1007/s12032-014-0111-8</identifier><identifier>PMID: 25001088</identifier><identifier>CODEN: MONCEZ</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Base Sequence ; Breast cancer ; Breast Neoplasms - genetics ; Case-Control Studies ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Hematology ; Humans ; Internal Medicine ; Iran ; Medicine ; Medicine & Public Health ; Membrane Proteins - genetics ; Middle Aged ; Molecular Sequence Data ; Odds Ratio ; Oncogene Proteins - genetics ; Oncology ; Original Paper ; Pathology</subject><ispartof>Medical oncology (Northwood, London, England), 2014-08, Vol.31 (8), p.111-111, Article 111</ispartof><rights>Springer Science+Business Media New York 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-cabb171f25d20df42c4c396c53695c49fa4dc7319fb96e6a0ad77a0f26bda1793</citedby><cites>FETCH-LOGICAL-c405t-cabb171f25d20df42c4c396c53695c49fa4dc7319fb96e6a0ad77a0f26bda1793</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/25001088$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hashemi, Mohammad</creatorcontrib><creatorcontrib>Amininia, Sahadi</creatorcontrib><creatorcontrib>Ebrahimi, Mahboubeh</creatorcontrib><creatorcontrib>Hashemi, Seyed Mehdi</creatorcontrib><creatorcontrib>Yousefi, Javad</creatorcontrib><creatorcontrib>Eskandari-Nasab, Ebrahim</creatorcontrib><creatorcontrib>Taheri, Mohsen</creatorcontrib><creatorcontrib>Ghavami, Saeid</creatorcontrib><title>Association between LAPTM4B gene polymorphism and breast cancer susceptibility in an Iranian population</title><title>Medical oncology (Northwood, London, England)</title><addtitle>Med Oncol</addtitle><addtitle>Med Oncol</addtitle><description>Lysosome associated protein transmembrane 4beta (LAPTM4B) contribute to the risk of numerous cancers. The present study focused on the possible association between
LAPTM4B
polymorphism and the risk of breast cancer (BC) in an Iranian population in southeast Iran. This case control study includes 311 BC patients and 225 healthy women. Genomic DNA was extracted from the whole blood by salting out method and
LAPTM4B
genotype was investigated using polymerase chain reaction. Our findings showed that
LAPTM4B
genotype was not associated with the risk of BC in any inheritance model tested. The minor allele frequency in case and control group was 0.297 and 0.278, respectively. The minor allele (LAPTM4B*2) was not associated with BC risk in comparison with
LAPTM4B*1
allele (odds ratio 1.10, 95 % confidence intervals 0.84–1.44,
p
= 0.495). Moreover,
LAPTM4B
polymorphism was not associated with clinical and pathological characteristics in the patient group. In conclusion, the findings of our study suggested that the polymorphism of
LAPTM4B
gene was not associated with susceptibility to BC and clinicopathological characteristics in an Iranian population.</description><subject>Base Sequence</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genetic Predisposition to Disease</subject><subject>Hematology</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Iran</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Membrane Proteins - genetics</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Odds Ratio</subject><subject>Oncogene Proteins - genetics</subject><subject>Oncology</subject><subject>Original Paper</subject><subject>Pathology</subject><issn>1357-0560</issn><issn>1559-131X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkU2LFDEQhhtR3A_9AV4k4MVLa1W-unMcF10XZtk9rOAtpNPpMUt30ibdyPx7M84qIsgeQgXqqTcpnqp6hfAOAZr3GSkwWgPychDr9kl1ikKoGhl-fVruTDQ1CAkn1VnO9wAUBVXPqxMqABDa9rTabXKO1pvFx0A6t_xwLpDt5vbumn8gOxccmeO4n2Kav_k8ERN60iVn8kKsCdYlktds3bz4zo9-2RMfCkOukgm-1DnO6_gr-0X1bDBjdi8f6nn15dPHu4vP9fbm8upis60tB7HU1nQdNjhQ0VPoB04tt0xJK5hUwnI1GN7bhqEaOiWdNGD6pjEwUNn1BhvFzqu3x9w5xe-ry4uefPngOJrg4po1SqZU23JJH0cFLywHekDf_IPexzWFskihBEjOqMJC4ZGyKeac3KDn5CeT9hpBH4TpozBdhOmDMN2WmdcPyWs3uf7PxG9DBaBHIJdW2Ln019P_Tf0Jrk2gRQ</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Hashemi, Mohammad</creator><creator>Amininia, Sahadi</creator><creator>Ebrahimi, Mahboubeh</creator><creator>Hashemi, Seyed Mehdi</creator><creator>Yousefi, Javad</creator><creator>Eskandari-Nasab, Ebrahim</creator><creator>Taheri, Mohsen</creator><creator>Ghavami, Saeid</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20140801</creationdate><title>Association between LAPTM4B gene polymorphism and breast cancer susceptibility in an Iranian population</title><author>Hashemi, Mohammad ; Amininia, Sahadi ; Ebrahimi, Mahboubeh ; Hashemi, Seyed Mehdi ; Yousefi, Javad ; Eskandari-Nasab, Ebrahim ; Taheri, Mohsen ; Ghavami, Saeid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-cabb171f25d20df42c4c396c53695c49fa4dc7319fb96e6a0ad77a0f26bda1793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Base Sequence</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genetic Predisposition to Disease</topic><topic>Hematology</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Iran</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Membrane Proteins - genetics</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>Odds Ratio</topic><topic>Oncogene Proteins - genetics</topic><topic>Oncology</topic><topic>Original Paper</topic><topic>Pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashemi, Mohammad</creatorcontrib><creatorcontrib>Amininia, Sahadi</creatorcontrib><creatorcontrib>Ebrahimi, Mahboubeh</creatorcontrib><creatorcontrib>Hashemi, Seyed Mehdi</creatorcontrib><creatorcontrib>Yousefi, Javad</creatorcontrib><creatorcontrib>Eskandari-Nasab, Ebrahim</creatorcontrib><creatorcontrib>Taheri, Mohsen</creatorcontrib><creatorcontrib>Ghavami, Saeid</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Medical oncology (Northwood, London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashemi, Mohammad</au><au>Amininia, Sahadi</au><au>Ebrahimi, Mahboubeh</au><au>Hashemi, Seyed Mehdi</au><au>Yousefi, Javad</au><au>Eskandari-Nasab, Ebrahim</au><au>Taheri, Mohsen</au><au>Ghavami, Saeid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between LAPTM4B gene polymorphism and breast cancer susceptibility in an Iranian population</atitle><jtitle>Medical oncology (Northwood, London, England)</jtitle><stitle>Med Oncol</stitle><addtitle>Med Oncol</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>31</volume><issue>8</issue><spage>111</spage><epage>111</epage><pages>111-111</pages><artnum>111</artnum><issn>1357-0560</issn><eissn>1559-131X</eissn><coden>MONCEZ</coden><abstract>Lysosome associated protein transmembrane 4beta (LAPTM4B) contribute to the risk of numerous cancers. The present study focused on the possible association between
LAPTM4B
polymorphism and the risk of breast cancer (BC) in an Iranian population in southeast Iran. This case control study includes 311 BC patients and 225 healthy women. Genomic DNA was extracted from the whole blood by salting out method and
LAPTM4B
genotype was investigated using polymerase chain reaction. Our findings showed that
LAPTM4B
genotype was not associated with the risk of BC in any inheritance model tested. The minor allele frequency in case and control group was 0.297 and 0.278, respectively. The minor allele (LAPTM4B*2) was not associated with BC risk in comparison with
LAPTM4B*1
allele (odds ratio 1.10, 95 % confidence intervals 0.84–1.44,
p
= 0.495). Moreover,
LAPTM4B
polymorphism was not associated with clinical and pathological characteristics in the patient group. In conclusion, the findings of our study suggested that the polymorphism of
LAPTM4B
gene was not associated with susceptibility to BC and clinicopathological characteristics in an Iranian population.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>25001088</pmid><doi>10.1007/s12032-014-0111-8</doi><tpages>1</tpages></addata></record> |
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language | eng |
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source | Springer Nature |
subjects | Base Sequence Breast cancer Breast Neoplasms - genetics Case-Control Studies Female Gene Frequency Genetic Predisposition to Disease Hematology Humans Internal Medicine Iran Medicine Medicine & Public Health Membrane Proteins - genetics Middle Aged Molecular Sequence Data Odds Ratio Oncogene Proteins - genetics Oncology Original Paper Pathology |
title | Association between LAPTM4B gene polymorphism and breast cancer susceptibility in an Iranian population |
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