Ki-ras proto-oncogene mutations in sporadic colorectal adenomas: Relationship to histologic and clinical characteristics
Background & Aims: The goal of this study was to examine the relationship between Ki-ras mutations in colorectal adenomas and characteristics of both the subject (age, gender, and family/personal history of colonic neoplasia) and the adenoma (multiplicity, size, location, and histologic features...
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creator | Maltzman, Terese Knoll, Kirsten Martinez, Maria Elena Byers, Tim Stevens, Beth R. Marshall, James R. Reid, Mary E. Einspahr, Janine Hart, Nancy Bhattacharyya, Achyut K. Kramer, Cheryl B. Sampliner, Richard Alberts, David S. Ahnen, Dennis J. |
description | Background & Aims: The goal of this study was to examine the relationship between Ki-ras mutations in colorectal adenomas and characteristics of both the subject (age, gender, and family/personal history of colonic neoplasia) and the adenoma (multiplicity, size, location, and histologic features).Methods: Ki-ras mutations were detected by direct sequencing in 738 adenomatous polyps removed at baseline from 639 participants in a nutritional trial of adenoma recurrence.Results: Ki-ras mutations were detected in 17.2% of the adenomas.Ki-ras mutations were unrelated to gender, family, or personal history of colonic neoplasia, location within the colorectum, or adenoma multiplicity, but were more common in older subjects (P = 0.01 for trend), in larger adenomas (P < 0.0001 for trend), in adenomas with villous histology (odds ratio [OR], 3.2; 95% confidence interval [CI], 2.1–4.9 vs.tubular), and in adenomas with high-grade dysplasia (32.0% vs.13.6%; OR, 3.0; 95% CI, 1.9–4.6 vs.low-grade dysplasia).Multivariate analysis showed Ki-ras mutations to be independently associated with subject age (P = 0.01 for trend), tubulovillous/villous histology (OR, 2.3; 95% CI, 1.5–3.7), and high-grade dysplasia (OR, 1.9; 95% CI, 1.2–3.1).Adenoma size was not independently related to Ki-ras mutation.Conclusions: Ki-ras mutations are associated with the histologic features of adenoma progression (villous histology and high-grade dysplasia) rather than with adenoma growth.
GASTROENTEROLOGY 2001;121:302-309 |
doi_str_mv | 10.1053/gast.2001.26278 |
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GASTROENTEROLOGY 2001;121:302-309</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/gast.2001.26278</identifier><identifier>PMID: 11487539</identifier><identifier>CODEN: GASTAB</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adenoma - genetics ; Adenoma - pathology ; Aged ; Biological and medical sciences ; Colorectal Neoplasms - epidemiology ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - pathology ; Digestive system ; DNA Mutational Analysis ; Female ; Genes, ras - genetics ; Genetic Predisposition to Disease ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Mutation ; Neoplasm Recurrence, Local ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Prevalence</subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2001-08, Vol.121 (2), p.302-309</ispartof><rights>2001 American Gastroenterological Association</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-5765e3bfc7e4e1ef2e68550009c8171ae89b6c72288b5446068871d16a491f5d3</citedby><cites>FETCH-LOGICAL-c479t-5765e3bfc7e4e1ef2e68550009c8171ae89b6c72288b5446068871d16a491f5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/gast.2001.26278$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1087209$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11487539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maltzman, Terese</creatorcontrib><creatorcontrib>Knoll, Kirsten</creatorcontrib><creatorcontrib>Martinez, Maria Elena</creatorcontrib><creatorcontrib>Byers, Tim</creatorcontrib><creatorcontrib>Stevens, Beth R.</creatorcontrib><creatorcontrib>Marshall, James R.</creatorcontrib><creatorcontrib>Reid, Mary E.</creatorcontrib><creatorcontrib>Einspahr, Janine</creatorcontrib><creatorcontrib>Hart, Nancy</creatorcontrib><creatorcontrib>Bhattacharyya, Achyut K.</creatorcontrib><creatorcontrib>Kramer, Cheryl B.</creatorcontrib><creatorcontrib>Sampliner, Richard</creatorcontrib><creatorcontrib>Alberts, David S.</creatorcontrib><creatorcontrib>Ahnen, Dennis J.</creatorcontrib><title>Ki-ras proto-oncogene mutations in sporadic colorectal adenomas: Relationship to histologic and clinical characteristics</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>Background & Aims: The goal of this study was to examine the relationship between Ki-ras mutations in colorectal adenomas and characteristics of both the subject (age, gender, and family/personal history of colonic neoplasia) and the adenoma (multiplicity, size, location, and histologic features).Methods: Ki-ras mutations were detected by direct sequencing in 738 adenomatous polyps removed at baseline from 639 participants in a nutritional trial of adenoma recurrence.Results: Ki-ras mutations were detected in 17.2% of the adenomas.Ki-ras mutations were unrelated to gender, family, or personal history of colonic neoplasia, location within the colorectum, or adenoma multiplicity, but were more common in older subjects (P = 0.01 for trend), in larger adenomas (P < 0.0001 for trend), in adenomas with villous histology (odds ratio [OR], 3.2; 95% confidence interval [CI], 2.1–4.9 vs.tubular), and in adenomas with high-grade dysplasia (32.0% vs.13.6%; OR, 3.0; 95% CI, 1.9–4.6 vs.low-grade dysplasia).Multivariate analysis showed Ki-ras mutations to be independently associated with subject age (P = 0.01 for trend), tubulovillous/villous histology (OR, 2.3; 95% CI, 1.5–3.7), and high-grade dysplasia (OR, 1.9; 95% CI, 1.2–3.1).Adenoma size was not independently related to Ki-ras mutation.Conclusions: Ki-ras mutations are associated with the histologic features of adenoma progression (villous histology and high-grade dysplasia) rather than with adenoma growth.
GASTROENTEROLOGY 2001;121:302-309</description><subject>Adenoma - genetics</subject><subject>Adenoma - pathology</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Colorectal Neoplasms - epidemiology</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Digestive system</subject><subject>DNA Mutational Analysis</subject><subject>Female</subject><subject>Genes, ras - genetics</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mutation</subject><subject>Neoplasm Recurrence, Local</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Prevalence</subject><issn>0016-5085</issn><issn>1528-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE2LFDEQhoMo7rh69iY5iLeeTbo7H-1NFr9wQRA9h0x19UykOxlTmUX_vWlnQC-eCqqeeql6GHsuxVYK1d3sPZVtK4Tctro19gHbSNXapjbah2xTi26UsOqKPSH6LoQYOisfsyspe2tUN2zYz0-hyZ74MaeSmhQh7TEiX07Fl5Ai8RA5HVP2YwAOaU4ZofiZ-xFjWjy95l9wPqOHcOQl8UOgUrl95X0cOcwhBqgbcPDZQ8Fc5wHoKXs0-Znw2aVes2_v3n69_dDcfX7_8fbNXQO9GUqjjFbY7SYw2KPEqUVtlVo_ASuN9GiHnQbTttbuVN9roa01cpTa94Oc1Nhds1fn3PrhjxNScUsgwHn2EdOJnKketTC6gjdnEHIiyji5Yw6Lz7-cFG6V7VbZbpXt_siuGy8u0afdguNf_mK3Ai8vgKeqYMo-QqB_cq1pxYoNZwyrh_uA2REEjIBjWG27MYX_3vAbnyOc7g</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Maltzman, Terese</creator><creator>Knoll, Kirsten</creator><creator>Martinez, Maria Elena</creator><creator>Byers, Tim</creator><creator>Stevens, Beth R.</creator><creator>Marshall, James R.</creator><creator>Reid, Mary E.</creator><creator>Einspahr, Janine</creator><creator>Hart, Nancy</creator><creator>Bhattacharyya, Achyut K.</creator><creator>Kramer, Cheryl B.</creator><creator>Sampliner, Richard</creator><creator>Alberts, David S.</creator><creator>Ahnen, Dennis J.</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>20010801</creationdate><title>Ki-ras proto-oncogene mutations in sporadic colorectal adenomas: Relationship to histologic and clinical characteristics</title><author>Maltzman, Terese ; Knoll, Kirsten ; Martinez, Maria Elena ; Byers, Tim ; Stevens, Beth R. ; Marshall, James R. ; Reid, Mary E. ; Einspahr, Janine ; Hart, Nancy ; Bhattacharyya, Achyut K. ; Kramer, Cheryl B. ; Sampliner, Richard ; Alberts, David S. ; Ahnen, Dennis J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-5765e3bfc7e4e1ef2e68550009c8171ae89b6c72288b5446068871d16a491f5d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adenoma - genetics</topic><topic>Adenoma - pathology</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Colorectal Neoplasms - epidemiology</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Digestive system</topic><topic>DNA Mutational Analysis</topic><topic>Female</topic><topic>Genes, ras - genetics</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mutation</topic><topic>Neoplasm Recurrence, Local</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Prevalence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maltzman, Terese</creatorcontrib><creatorcontrib>Knoll, Kirsten</creatorcontrib><creatorcontrib>Martinez, Maria Elena</creatorcontrib><creatorcontrib>Byers, Tim</creatorcontrib><creatorcontrib>Stevens, Beth R.</creatorcontrib><creatorcontrib>Marshall, James R.</creatorcontrib><creatorcontrib>Reid, Mary E.</creatorcontrib><creatorcontrib>Einspahr, Janine</creatorcontrib><creatorcontrib>Hart, Nancy</creatorcontrib><creatorcontrib>Bhattacharyya, Achyut K.</creatorcontrib><creatorcontrib>Kramer, Cheryl B.</creatorcontrib><creatorcontrib>Sampliner, Richard</creatorcontrib><creatorcontrib>Alberts, David S.</creatorcontrib><creatorcontrib>Ahnen, Dennis J.</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>Gastroenterology (New York, N.Y. 1943)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maltzman, Terese</au><au>Knoll, Kirsten</au><au>Martinez, Maria Elena</au><au>Byers, Tim</au><au>Stevens, Beth R.</au><au>Marshall, James R.</au><au>Reid, Mary E.</au><au>Einspahr, Janine</au><au>Hart, Nancy</au><au>Bhattacharyya, Achyut K.</au><au>Kramer, Cheryl B.</au><au>Sampliner, Richard</au><au>Alberts, David S.</au><au>Ahnen, Dennis J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ki-ras proto-oncogene mutations in sporadic colorectal adenomas: Relationship to histologic and clinical characteristics</atitle><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle><addtitle>Gastroenterology</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>121</volume><issue>2</issue><spage>302</spage><epage>309</epage><pages>302-309</pages><issn>0016-5085</issn><eissn>1528-0012</eissn><coden>GASTAB</coden><abstract>Background & Aims: The goal of this study was to examine the relationship between Ki-ras mutations in colorectal adenomas and characteristics of both the subject (age, gender, and family/personal history of colonic neoplasia) and the adenoma (multiplicity, size, location, and histologic features).Methods: Ki-ras mutations were detected by direct sequencing in 738 adenomatous polyps removed at baseline from 639 participants in a nutritional trial of adenoma recurrence.Results: Ki-ras mutations were detected in 17.2% of the adenomas.Ki-ras mutations were unrelated to gender, family, or personal history of colonic neoplasia, location within the colorectum, or adenoma multiplicity, but were more common in older subjects (P = 0.01 for trend), in larger adenomas (P < 0.0001 for trend), in adenomas with villous histology (odds ratio [OR], 3.2; 95% confidence interval [CI], 2.1–4.9 vs.tubular), and in adenomas with high-grade dysplasia (32.0% vs.13.6%; OR, 3.0; 95% CI, 1.9–4.6 vs.low-grade dysplasia).Multivariate analysis showed Ki-ras mutations to be independently associated with subject age (P = 0.01 for trend), tubulovillous/villous histology (OR, 2.3; 95% CI, 1.5–3.7), and high-grade dysplasia (OR, 1.9; 95% CI, 1.2–3.1).Adenoma size was not independently related to Ki-ras mutation.Conclusions: Ki-ras mutations are associated with the histologic features of adenoma progression (villous histology and high-grade dysplasia) rather than with adenoma growth.
GASTROENTEROLOGY 2001;121:302-309</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>11487539</pmid><doi>10.1053/gast.2001.26278</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenoma - genetics Adenoma - pathology Aged Biological and medical sciences Colorectal Neoplasms - epidemiology Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology Digestive system DNA Mutational Analysis Female Genes, ras - genetics Genetic Predisposition to Disease Humans Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Mutation Neoplasm Recurrence, Local Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Prevalence |
title | Ki-ras proto-oncogene mutations in sporadic colorectal adenomas: Relationship to histologic and clinical characteristics |
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