Genetic Loci Controlling Breast Cancer Susceptibility in the Wistar-Kyoto Rat
In this study, the Wistar-Kyoto (WKy) rat was genetically characterized for loci that modify susceptibility to mammary carcinogenesis. We used a genetic backcross between resistant WKy and susceptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinoma sus...
Gespeichert in:
Veröffentlicht in: | Genetics (Austin) 2001-01, Vol.157 (1), p.331-339 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 339 |
---|---|
container_issue | 1 |
container_start_page | 331 |
container_title | Genetics (Austin) |
container_volume | 157 |
creator | Lan, Hong Kendziorski, Christina M Haag, Jill D Shepel, Laurie A Newton, Michael A Gould, Michael N |
description | In this study, the Wistar-Kyoto (WKy) rat was genetically characterized for loci that modify susceptibility to mammary carcinogenesis. We used a genetic backcross between resistant WKy and susceptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinoma susceptibility (Mcs) loci underlying the resistance of the WKy rat. Rats were phenotyped for DMBA-induced mammary carcinomas and genotyped using microsatellite markers. To detect quantitative trait loci (QTL), we analyzed the genome scan data under both parametric and nonparametric distributional assumptions and used permutation tests to calculate significance thresholds. A generalized linear model analysis was also performed to test for interactions between significant QTL. This methodology was extended to identify interactions between the significant QTL and other genome locations. Chromosomes 5, 7, 10, and 14 were found to contain significant QTL, termed Mcs5, Mcs6, Mcs7, and Mcs8, respectively. The WKy alleles of Mcs5, -6, and -8 are associated with mammary carcinoma resistance; the WKy allele of Mcs7 is associated with an increased incidence of mammary cancer. In addition, we identified an interaction between Mcs8 and a region on chromosome 6 termed Mcsm1 (modifier of Mcs), which had no significant main effect on mammary cancer susceptibility in this genetic analysis. |
doi_str_mv | 10.1093/genetics/157.1.331 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1461476</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69559226</sourcerecordid><originalsourceid>FETCH-LOGICAL-c456t-c2788ebbcfddb59672950e158a9a7352c200bad80482974805458478f92ff72f3</originalsourceid><addsrcrecordid>eNpVkc1uEzEUhS0EomnhBVggiwW7SX39M7Y3SG1EW0QQEj9iaXkcT-JqMk5tp1Hevq4SaFndhb_73SMfhN4BmQLR7HzpR1-Cy-cg5BSmjMELNAHNWUNbBi_RhBBom1YyOEGnOd8SQlot1Gt0AgBMC2AT9O36IMHz6AKexbGkOAxhXOLL5G0ueGZH5xP-uc3Ob0rowhDKHocRl5XHf0IuNjVf97FE_MOWN-hVb4fs3x7nGfp99fnX7KaZf7_-MruYN46LtjSOSqV817l-seiEbiXVgngQymormaCOEtLZhSJcUS25IoILxaXqNe17SXt2hj4dvJttt_YL52tsO5hNCmub9ibaYP5_GcPKLOO9Ad4Cl20VfDgKUrzb-lzMbdymsWY2FDhQUhNUiB4gl2LOyff_DgAxjw2Yvw2Y2oABUxuoS--fR3taOX55BT4egFVYrnYheZPXdhgqDma32z2ZHgC2cZF3</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>214120200</pqid></control><display><type>article</type><title>Genetic Loci Controlling Breast Cancer Susceptibility in the Wistar-Kyoto Rat</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Lan, Hong ; Kendziorski, Christina M ; Haag, Jill D ; Shepel, Laurie A ; Newton, Michael A ; Gould, Michael N</creator><creatorcontrib>Lan, Hong ; Kendziorski, Christina M ; Haag, Jill D ; Shepel, Laurie A ; Newton, Michael A ; Gould, Michael N</creatorcontrib><description>In this study, the Wistar-Kyoto (WKy) rat was genetically characterized for loci that modify susceptibility to mammary carcinogenesis. We used a genetic backcross between resistant WKy and susceptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinoma susceptibility (Mcs) loci underlying the resistance of the WKy rat. Rats were phenotyped for DMBA-induced mammary carcinomas and genotyped using microsatellite markers. To detect quantitative trait loci (QTL), we analyzed the genome scan data under both parametric and nonparametric distributional assumptions and used permutation tests to calculate significance thresholds. A generalized linear model analysis was also performed to test for interactions between significant QTL. This methodology was extended to identify interactions between the significant QTL and other genome locations. Chromosomes 5, 7, 10, and 14 were found to contain significant QTL, termed Mcs5, Mcs6, Mcs7, and Mcs8, respectively. The WKy alleles of Mcs5, -6, and -8 are associated with mammary carcinoma resistance; the WKy allele of Mcs7 is associated with an increased incidence of mammary cancer. In addition, we identified an interaction between Mcs8 and a region on chromosome 6 termed Mcsm1 (modifier of Mcs), which had no significant main effect on mammary cancer susceptibility in this genetic analysis.</description><identifier>ISSN: 0016-6731</identifier><identifier>ISSN: 1943-2631</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/157.1.331</identifier><identifier>PMID: 11139513</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>United States: Genetics Soc America</publisher><subject>9,10-Dimethyl-1,2-benzanthracene - toxicity ; Animals ; Breast cancer ; Carcinogens - toxicity ; Crosses, Genetic ; Female ; Genes ; Genes, Tumor Suppressor ; Genetics ; Genotype ; Humans ; Male ; Mammary Neoplasms, Experimental - chemically induced ; Mammary Neoplasms, Experimental - genetics ; Models, Genetic ; Oncogenes ; Quantitative Trait, Heritable ; Rats ; Rats, Inbred WF ; Rats, Inbred WKY ; Rodents</subject><ispartof>Genetics (Austin), 2001-01, Vol.157 (1), p.331-339</ispartof><rights>Copyright Genetics Society of America Jan 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-c2788ebbcfddb59672950e158a9a7352c200bad80482974805458478f92ff72f3</citedby><cites>FETCH-LOGICAL-c456t-c2788ebbcfddb59672950e158a9a7352c200bad80482974805458478f92ff72f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11139513$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lan, Hong</creatorcontrib><creatorcontrib>Kendziorski, Christina M</creatorcontrib><creatorcontrib>Haag, Jill D</creatorcontrib><creatorcontrib>Shepel, Laurie A</creatorcontrib><creatorcontrib>Newton, Michael A</creatorcontrib><creatorcontrib>Gould, Michael N</creatorcontrib><title>Genetic Loci Controlling Breast Cancer Susceptibility in the Wistar-Kyoto Rat</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>In this study, the Wistar-Kyoto (WKy) rat was genetically characterized for loci that modify susceptibility to mammary carcinogenesis. We used a genetic backcross between resistant WKy and susceptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinoma susceptibility (Mcs) loci underlying the resistance of the WKy rat. Rats were phenotyped for DMBA-induced mammary carcinomas and genotyped using microsatellite markers. To detect quantitative trait loci (QTL), we analyzed the genome scan data under both parametric and nonparametric distributional assumptions and used permutation tests to calculate significance thresholds. A generalized linear model analysis was also performed to test for interactions between significant QTL. This methodology was extended to identify interactions between the significant QTL and other genome locations. Chromosomes 5, 7, 10, and 14 were found to contain significant QTL, termed Mcs5, Mcs6, Mcs7, and Mcs8, respectively. The WKy alleles of Mcs5, -6, and -8 are associated with mammary carcinoma resistance; the WKy allele of Mcs7 is associated with an increased incidence of mammary cancer. In addition, we identified an interaction between Mcs8 and a region on chromosome 6 termed Mcsm1 (modifier of Mcs), which had no significant main effect on mammary cancer susceptibility in this genetic analysis.</description><subject>9,10-Dimethyl-1,2-benzanthracene - toxicity</subject><subject>Animals</subject><subject>Breast cancer</subject><subject>Carcinogens - toxicity</subject><subject>Crosses, Genetic</subject><subject>Female</subject><subject>Genes</subject><subject>Genes, Tumor Suppressor</subject><subject>Genetics</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Mammary Neoplasms, Experimental - chemically induced</subject><subject>Mammary Neoplasms, Experimental - genetics</subject><subject>Models, Genetic</subject><subject>Oncogenes</subject><subject>Quantitative Trait, Heritable</subject><subject>Rats</subject><subject>Rats, Inbred WF</subject><subject>Rats, Inbred WKY</subject><subject>Rodents</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1uEzEUhS0EomnhBVggiwW7SX39M7Y3SG1EW0QQEj9iaXkcT-JqMk5tp1Hevq4SaFndhb_73SMfhN4BmQLR7HzpR1-Cy-cg5BSmjMELNAHNWUNbBi_RhBBom1YyOEGnOd8SQlot1Gt0AgBMC2AT9O36IMHz6AKexbGkOAxhXOLL5G0ueGZH5xP-uc3Ob0rowhDKHocRl5XHf0IuNjVf97FE_MOWN-hVb4fs3x7nGfp99fnX7KaZf7_-MruYN46LtjSOSqV817l-seiEbiXVgngQymormaCOEtLZhSJcUS25IoILxaXqNe17SXt2hj4dvJttt_YL52tsO5hNCmub9ibaYP5_GcPKLOO9Ad4Cl20VfDgKUrzb-lzMbdymsWY2FDhQUhNUiB4gl2LOyff_DgAxjw2Yvw2Y2oABUxuoS--fR3taOX55BT4egFVYrnYheZPXdhgqDma32z2ZHgC2cZF3</recordid><startdate>20010101</startdate><enddate>20010101</enddate><creator>Lan, Hong</creator><creator>Kendziorski, Christina M</creator><creator>Haag, Jill D</creator><creator>Shepel, Laurie A</creator><creator>Newton, Michael A</creator><creator>Gould, Michael N</creator><general>Genetics Soc America</general><general>Genetics Society of America</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>4T-</scope><scope>4U-</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20010101</creationdate><title>Genetic Loci Controlling Breast Cancer Susceptibility in the Wistar-Kyoto Rat</title><author>Lan, Hong ; Kendziorski, Christina M ; Haag, Jill D ; Shepel, Laurie A ; Newton, Michael A ; Gould, Michael N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-c2788ebbcfddb59672950e158a9a7352c200bad80482974805458478f92ff72f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>9,10-Dimethyl-1,2-benzanthracene - toxicity</topic><topic>Animals</topic><topic>Breast cancer</topic><topic>Carcinogens - toxicity</topic><topic>Crosses, Genetic</topic><topic>Female</topic><topic>Genes</topic><topic>Genes, Tumor Suppressor</topic><topic>Genetics</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Mammary Neoplasms, Experimental - chemically induced</topic><topic>Mammary Neoplasms, Experimental - genetics</topic><topic>Models, Genetic</topic><topic>Oncogenes</topic><topic>Quantitative Trait, Heritable</topic><topic>Rats</topic><topic>Rats, Inbred WF</topic><topic>Rats, Inbred WKY</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lan, Hong</creatorcontrib><creatorcontrib>Kendziorski, Christina M</creatorcontrib><creatorcontrib>Haag, Jill D</creatorcontrib><creatorcontrib>Shepel, Laurie A</creatorcontrib><creatorcontrib>Newton, Michael A</creatorcontrib><creatorcontrib>Gould, Michael N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lan, Hong</au><au>Kendziorski, Christina M</au><au>Haag, Jill D</au><au>Shepel, Laurie A</au><au>Newton, Michael A</au><au>Gould, Michael N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic Loci Controlling Breast Cancer Susceptibility in the Wistar-Kyoto Rat</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>2001-01-01</date><risdate>2001</risdate><volume>157</volume><issue>1</issue><spage>331</spage><epage>339</epage><pages>331-339</pages><issn>0016-6731</issn><issn>1943-2631</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>In this study, the Wistar-Kyoto (WKy) rat was genetically characterized for loci that modify susceptibility to mammary carcinogenesis. We used a genetic backcross between resistant WKy and susceptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinoma susceptibility (Mcs) loci underlying the resistance of the WKy rat. Rats were phenotyped for DMBA-induced mammary carcinomas and genotyped using microsatellite markers. To detect quantitative trait loci (QTL), we analyzed the genome scan data under both parametric and nonparametric distributional assumptions and used permutation tests to calculate significance thresholds. A generalized linear model analysis was also performed to test for interactions between significant QTL. This methodology was extended to identify interactions between the significant QTL and other genome locations. Chromosomes 5, 7, 10, and 14 were found to contain significant QTL, termed Mcs5, Mcs6, Mcs7, and Mcs8, respectively. The WKy alleles of Mcs5, -6, and -8 are associated with mammary carcinoma resistance; the WKy allele of Mcs7 is associated with an increased incidence of mammary cancer. In addition, we identified an interaction between Mcs8 and a region on chromosome 6 termed Mcsm1 (modifier of Mcs), which had no significant main effect on mammary cancer susceptibility in this genetic analysis.</abstract><cop>United States</cop><pub>Genetics Soc America</pub><pmid>11139513</pmid><doi>10.1093/genetics/157.1.331</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0016-6731 |
ispartof | Genetics (Austin), 2001-01, Vol.157 (1), p.331-339 |
issn | 0016-6731 1943-2631 1943-2631 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1461476 |
source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | 9,10-Dimethyl-1,2-benzanthracene - toxicity Animals Breast cancer Carcinogens - toxicity Crosses, Genetic Female Genes Genes, Tumor Suppressor Genetics Genotype Humans Male Mammary Neoplasms, Experimental - chemically induced Mammary Neoplasms, Experimental - genetics Models, Genetic Oncogenes Quantitative Trait, Heritable Rats Rats, Inbred WF Rats, Inbred WKY Rodents |
title | Genetic Loci Controlling Breast Cancer Susceptibility in the Wistar-Kyoto Rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T07%3A55%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetic%20Loci%20Controlling%20Breast%20Cancer%20Susceptibility%20in%20the%20Wistar-Kyoto%20Rat&rft.jtitle=Genetics%20(Austin)&rft.au=Lan,%20Hong&rft.date=2001-01-01&rft.volume=157&rft.issue=1&rft.spage=331&rft.epage=339&rft.pages=331-339&rft.issn=0016-6731&rft.eissn=1943-2631&rft.coden=GENTAE&rft_id=info:doi/10.1093/genetics/157.1.331&rft_dat=%3Cproquest_pubme%3E69559226%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=214120200&rft_id=info:pmid/11139513&rfr_iscdi=true |