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The Adenomatous Polyposis Coli (APC) gene microsatellite marker D5S1385 is equally informative for loss of heterozygosity as the marker D5S346
Molecular analyses for loss of heterozygosity (LOH) at a gene locus are used to identify genomic imbalance in tumor tissue. A frequently utilized microsatellite marker for the Adenomatous Polyposis Coli (APC) gene is denoted D5S346. However, when an individual has two identical forms of this microsa...
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Published in: | Experimental and molecular pathology 2003-10, Vol.75 (2), p.144-147 |
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description | Molecular analyses for loss of heterozygosity (LOH) at a gene locus are used to identify genomic imbalance in tumor tissue. A frequently utilized microsatellite marker for the Adenomatous Polyposis Coli (APC) gene is denoted D5S346. However, when an individual has two identical forms of this microsatellite, then a second microsatellite, also near the APC gene, is needed. We present data on an APC microsatellite marker designated D5S1385, located on the 5′ end of the APC gene, and we compare these to data utilizing the marker D5S346. Polymerase chain reaction (PCR) was used, followed by gel electrophoresis. Homozygosity for the marker D5S1385 was present in 55 individuals, or 28%. Thirty-seven carcinomas and 32 adenomas were assessed for LOH from individuals informative with both microsatellite markers. D5S1385 detected LOH in 39 of 41 lesions, or 95%, for which D5S346 detected LOH. D5S1385 is moderately polymorphic and is informative at least as often as D5S346. |
doi_str_mv | 10.1016/S0014-4800(03)00069-8 |
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A frequently utilized microsatellite marker for the Adenomatous Polyposis Coli (APC) gene is denoted D5S346. However, when an individual has two identical forms of this microsatellite, then a second microsatellite, also near the APC gene, is needed. We present data on an APC microsatellite marker designated D5S1385, located on the 5′ end of the APC gene, and we compare these to data utilizing the marker D5S346. Polymerase chain reaction (PCR) was used, followed by gel electrophoresis. Homozygosity for the marker D5S1385 was present in 55 individuals, or 28%. Thirty-seven carcinomas and 32 adenomas were assessed for LOH from individuals informative with both microsatellite markers. D5S1385 detected LOH in 39 of 41 lesions, or 95%, for which D5S346 detected LOH. D5S1385 is moderately polymorphic and is informative at least as often as D5S346.</description><identifier>ISSN: 0014-4800</identifier><identifier>EISSN: 1096-0945</identifier><identifier>DOI: 10.1016/S0014-4800(03)00069-8</identifier><identifier>PMID: 14516776</identifier><identifier>CODEN: EXMPA6</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adenomatous Polyposis Coli - genetics ; Adenomatous Polyposis Coli gene ; Adult ; Aged ; Aged, 80 and over ; Alleles ; Biological and medical sciences ; Colon carcinoma ; D5S1385 ; D5S346 ; DNA Primers - chemistry ; DNA, Neoplasm - analysis ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Genes, APC ; Genotype ; Homozygosity ; Humans ; Loss of heterozygosity ; Loss of Heterozygosity - genetics ; Male ; Medical sciences ; Microsatellite markers ; Microsatellite Repeats - genetics ; Middle Aged ; Mutation - genetics ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Experimental and molecular pathology, 2003-10, Vol.75 (2), p.144-147</ispartof><rights>2003 Elsevier Science (USA)</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-77c2373ed8e8024dcbfb6888e077751246a57b49ef44b893696958891ed3f7c63</citedby><cites>FETCH-LOGICAL-c391t-77c2373ed8e8024dcbfb6888e077751246a57b49ef44b893696958891ed3f7c63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15183645$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14516776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zauber, N.Peter</creatorcontrib><creatorcontrib>Sabbath-Solitare, Marlene</creatorcontrib><creatorcontrib>Marotta, Stephen P</creatorcontrib><creatorcontrib>Bishop, D.Timothy</creatorcontrib><title>The Adenomatous Polyposis Coli (APC) gene microsatellite marker D5S1385 is equally informative for loss of heterozygosity as the marker D5S346</title><title>Experimental and molecular pathology</title><addtitle>Exp Mol Pathol</addtitle><description>Molecular analyses for loss of heterozygosity (LOH) at a gene locus are used to identify genomic imbalance in tumor tissue. A frequently utilized microsatellite marker for the Adenomatous Polyposis Coli (APC) gene is denoted D5S346. However, when an individual has two identical forms of this microsatellite, then a second microsatellite, also near the APC gene, is needed. We present data on an APC microsatellite marker designated D5S1385, located on the 5′ end of the APC gene, and we compare these to data utilizing the marker D5S346. Polymerase chain reaction (PCR) was used, followed by gel electrophoresis. Homozygosity for the marker D5S1385 was present in 55 individuals, or 28%. Thirty-seven carcinomas and 32 adenomas were assessed for LOH from individuals informative with both microsatellite markers. D5S1385 detected LOH in 39 of 41 lesions, or 95%, for which D5S346 detected LOH. D5S1385 is moderately polymorphic and is informative at least as often as D5S346.</description><subject>Adenomatous Polyposis Coli - genetics</subject><subject>Adenomatous Polyposis Coli gene</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Colon carcinoma</subject><subject>D5S1385</subject><subject>D5S346</subject><subject>DNA Primers - chemistry</subject><subject>DNA, Neoplasm - analysis</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genes, APC</subject><subject>Genotype</subject><subject>Homozygosity</subject><subject>Humans</subject><subject>Loss of heterozygosity</subject><subject>Loss of Heterozygosity - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microsatellite markers</subject><subject>Microsatellite Repeats - genetics</subject><subject>Middle Aged</subject><subject>Mutation - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Genetic</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0014-4800</issn><issn>1096-0945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkUtv1DAUhS1ERaeFnwDyBtQuAnb8XqHRlEelSlRqWVuOc9MxZOKpnamU_oj-ZjwPUXasbEvfOT73XITeUvKREio_3RBCecU1IWeEnRNCpKn0CzSjxMiKGC5eotlf5Bid5PyrQIbQ-hU6plxQqZScoafbJeB5C0NcuTFuMr6O_bSOOWS8iH3AZ_PrxTm-gwHwKvgUsxuh78NYni79hoQvxA1lWuAigPuN6_sJh6GLqdiFB8DlhvuYM44dXsIIKT5Od8V-nLDLeFz-68O4fI2OOtdneHM4T9HPr19uF9-rqx_fLhfzq8ozQ8dKKV8zxaDVoEnNW990jdRaA1FKCVpz6YRquIGO80YbJo00QmtDoWWd8pKdog9733WK9xvIo12F7MtkboDSglVC1YRxUUCxB7ez5wSdXadQIk-WErtdhN0twm5btoTZ3SKsLrp3hw82zQraZ9Wh-QK8PwAue9d3yQ0-5GdOUM3kLsDnPQeljocAyWYfYPDQhgR-tG0M_4nyB_45pAA</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Zauber, N.Peter</creator><creator>Sabbath-Solitare, Marlene</creator><creator>Marotta, Stephen P</creator><creator>Bishop, D.Timothy</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20031001</creationdate><title>The Adenomatous Polyposis Coli (APC) gene microsatellite marker D5S1385 is equally informative for loss of heterozygosity as the marker D5S346</title><author>Zauber, N.Peter ; Sabbath-Solitare, Marlene ; Marotta, Stephen P ; Bishop, D.Timothy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-77c2373ed8e8024dcbfb6888e077751246a57b49ef44b893696958891ed3f7c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adenomatous Polyposis Coli - genetics</topic><topic>Adenomatous Polyposis Coli gene</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alleles</topic><topic>Biological and medical sciences</topic><topic>Colon carcinoma</topic><topic>D5S1385</topic><topic>D5S346</topic><topic>DNA Primers - chemistry</topic><topic>DNA, Neoplasm - analysis</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genes, APC</topic><topic>Genotype</topic><topic>Homozygosity</topic><topic>Humans</topic><topic>Loss of heterozygosity</topic><topic>Loss of Heterozygosity - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microsatellite markers</topic><topic>Microsatellite Repeats - genetics</topic><topic>Middle Aged</topic><topic>Mutation - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Genetic</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zauber, N.Peter</creatorcontrib><creatorcontrib>Sabbath-Solitare, Marlene</creatorcontrib><creatorcontrib>Marotta, Stephen P</creatorcontrib><creatorcontrib>Bishop, D.Timothy</creatorcontrib><collection>Pascal-Francis</collection><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>Experimental and molecular pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zauber, N.Peter</au><au>Sabbath-Solitare, Marlene</au><au>Marotta, Stephen P</au><au>Bishop, D.Timothy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Adenomatous Polyposis Coli (APC) gene microsatellite marker D5S1385 is equally informative for loss of heterozygosity as the marker D5S346</atitle><jtitle>Experimental and molecular pathology</jtitle><addtitle>Exp Mol Pathol</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>75</volume><issue>2</issue><spage>144</spage><epage>147</epage><pages>144-147</pages><issn>0014-4800</issn><eissn>1096-0945</eissn><coden>EXMPA6</coden><abstract>Molecular analyses for loss of heterozygosity (LOH) at a gene locus are used to identify genomic imbalance in tumor tissue. A frequently utilized microsatellite marker for the Adenomatous Polyposis Coli (APC) gene is denoted D5S346. However, when an individual has two identical forms of this microsatellite, then a second microsatellite, also near the APC gene, is needed. We present data on an APC microsatellite marker designated D5S1385, located on the 5′ end of the APC gene, and we compare these to data utilizing the marker D5S346. Polymerase chain reaction (PCR) was used, followed by gel electrophoresis. Homozygosity for the marker D5S1385 was present in 55 individuals, or 28%. Thirty-seven carcinomas and 32 adenomas were assessed for LOH from individuals informative with both microsatellite markers. D5S1385 detected LOH in 39 of 41 lesions, or 95%, for which D5S346 detected LOH. D5S1385 is moderately polymorphic and is informative at least as often as D5S346.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>14516776</pmid><doi>10.1016/S0014-4800(03)00069-8</doi><tpages>4</tpages></addata></record> |
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subjects | Adenomatous Polyposis Coli - genetics Adenomatous Polyposis Coli gene Adult Aged Aged, 80 and over Alleles Biological and medical sciences Colon carcinoma D5S1385 D5S346 DNA Primers - chemistry DNA, Neoplasm - analysis Female Gastroenterology. Liver. Pancreas. Abdomen Genes, APC Genotype Homozygosity Humans Loss of heterozygosity Loss of Heterozygosity - genetics Male Medical sciences Microsatellite markers Microsatellite Repeats - genetics Middle Aged Mutation - genetics Polymerase Chain Reaction Polymorphism, Genetic Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | The Adenomatous Polyposis Coli (APC) gene microsatellite marker D5S1385 is equally informative for loss of heterozygosity as the marker D5S346 |
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