Association of polymorphisms in the beta-2 and beta-3 adrenoceptor genes with risk of colorectal cancer in Japanese
The adrenergic receptor system is involved in thermogenesis and in the activation of lipid mobilization in fat cells, and polymorphisms in the beta-2 and beta-3 adrenoceptor genes (BAR2 and BAR3) have been reported to be associated with obesity and insulin resistance. To examine links between polymo...
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Veröffentlicht in: | International journal of clinical oncology 2001-06, Vol.6 (3), p.117-122 |
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creator | Takezaki, T Hamajima, N Matsuo, K Tanaka, R Hirai, T Kato, T Ohashi, K Tajima, K |
description | The adrenergic receptor system is involved in thermogenesis and in the activation of lipid mobilization in fat cells, and polymorphisms in the beta-2 and beta-3 adrenoceptor genes (BAR2 and BAR3) have been reported to be associated with obesity and insulin resistance. To examine links between polymorphisms in these genes and the risk of colorectal cancer in Japanese, we conducted the present hospital-based case-referent study.
Mutations of the BAR2 gene at codon 27 (Gln27Glu) and of the BAR3 gene at codon 64 (Trp64Arg) were examined in 131 patients with colorectal cancer (cases) and in 239 cancer-free referents. We also collected information on environmental factors, using a questionnaire approach. Odds ratios (ORs) were estimated with an unconditional logistic model, after adjustment for potential confounding factors.
The proportional distribution of the mutations in BAR2 and BAR3 did not differ between cases and referents. Analysis of a subgroup with a higher body mass index showed that the Trp64Arg variant increased the OR (2.63; 95% confidence interval, 1.13-6.11) for colon cancer, but not for rectal cancer, compared with the Trp64 genotype. Altered ORs for colon and rectal cancers with the Gln27Glu variant were not observed in either the subgroup with the lower body mass index or the subgroup with the higher body mass index.
These findings suggest that the BAR3 polymorphism may alter the susceptibility to colon cancer risk in obese subjects. To confirm this finding, a further study with a larger number of subjects is now required. |
doi_str_mv | 10.1007/PL00012092 |
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Mutations of the BAR2 gene at codon 27 (Gln27Glu) and of the BAR3 gene at codon 64 (Trp64Arg) were examined in 131 patients with colorectal cancer (cases) and in 239 cancer-free referents. We also collected information on environmental factors, using a questionnaire approach. Odds ratios (ORs) were estimated with an unconditional logistic model, after adjustment for potential confounding factors.
The proportional distribution of the mutations in BAR2 and BAR3 did not differ between cases and referents. Analysis of a subgroup with a higher body mass index showed that the Trp64Arg variant increased the OR (2.63; 95% confidence interval, 1.13-6.11) for colon cancer, but not for rectal cancer, compared with the Trp64 genotype. Altered ORs for colon and rectal cancers with the Gln27Glu variant were not observed in either the subgroup with the lower body mass index or the subgroup with the higher body mass index.
These findings suggest that the BAR3 polymorphism may alter the susceptibility to colon cancer risk in obese subjects. To confirm this finding, a further study with a larger number of subjects is now required.</description><identifier>ISSN: 1341-9625</identifier><identifier>EISSN: 1437-7772</identifier><identifier>DOI: 10.1007/PL00012092</identifier><identifier>PMID: 11706779</identifier><language>eng</language><publisher>Japan: Springer Nature B.V</publisher><subject>Adult ; Aged ; Body Mass Index ; Case-Control Studies ; Colorectal cancer ; Colorectal Neoplasms - ethnology ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - pathology ; Confidence intervals ; DNA, Neoplasm - genetics ; Female ; Genes ; Genetic Predisposition to Disease ; Humans ; Insulin Resistance ; Japan - epidemiology ; Japan - ethnology ; Male ; Middle Aged ; Mutation ; Obesity ; Polymorphism, Genetic ; Receptors, Adrenergic, beta-2 - genetics ; Receptors, Adrenergic, beta-3 - genetics ; Risk Factors</subject><ispartof>International journal of clinical oncology, 2001-06, Vol.6 (3), p.117-122</ispartof><rights>The Japan Society of Clinical Oncology 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c279t-a7ba5d1196d32fec18fd5c0774a06df81b0f0adf81ae77b9a46bf815a416a4c03</citedby></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/11706779$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takezaki, T</creatorcontrib><creatorcontrib>Hamajima, N</creatorcontrib><creatorcontrib>Matsuo, K</creatorcontrib><creatorcontrib>Tanaka, R</creatorcontrib><creatorcontrib>Hirai, T</creatorcontrib><creatorcontrib>Kato, T</creatorcontrib><creatorcontrib>Ohashi, K</creatorcontrib><creatorcontrib>Tajima, K</creatorcontrib><title>Association of polymorphisms in the beta-2 and beta-3 adrenoceptor genes with risk of colorectal cancer in Japanese</title><title>International journal of clinical oncology</title><addtitle>Int J Clin Oncol</addtitle><description>The adrenergic receptor system is involved in thermogenesis and in the activation of lipid mobilization in fat cells, and polymorphisms in the beta-2 and beta-3 adrenoceptor genes (BAR2 and BAR3) have been reported to be associated with obesity and insulin resistance. To examine links between polymorphisms in these genes and the risk of colorectal cancer in Japanese, we conducted the present hospital-based case-referent study.
Mutations of the BAR2 gene at codon 27 (Gln27Glu) and of the BAR3 gene at codon 64 (Trp64Arg) were examined in 131 patients with colorectal cancer (cases) and in 239 cancer-free referents. We also collected information on environmental factors, using a questionnaire approach. Odds ratios (ORs) were estimated with an unconditional logistic model, after adjustment for potential confounding factors.
The proportional distribution of the mutations in BAR2 and BAR3 did not differ between cases and referents. Analysis of a subgroup with a higher body mass index showed that the Trp64Arg variant increased the OR (2.63; 95% confidence interval, 1.13-6.11) for colon cancer, but not for rectal cancer, compared with the Trp64 genotype. Altered ORs for colon and rectal cancers with the Gln27Glu variant were not observed in either the subgroup with the lower body mass index or the subgroup with the higher body mass index.
These findings suggest that the BAR3 polymorphism may alter the susceptibility to colon cancer risk in obese subjects. To confirm this finding, a further study with a larger number of subjects is now required.</description><subject>Adult</subject><subject>Aged</subject><subject>Body Mass Index</subject><subject>Case-Control Studies</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - ethnology</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Confidence intervals</subject><subject>DNA, Neoplasm - genetics</subject><subject>Female</subject><subject>Genes</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Insulin Resistance</subject><subject>Japan - epidemiology</subject><subject>Japan - ethnology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Obesity</subject><subject>Polymorphism, Genetic</subject><subject>Receptors, Adrenergic, beta-2 - genetics</subject><subject>Receptors, Adrenergic, beta-3 - genetics</subject><subject>Risk Factors</subject><issn>1341-9625</issn><issn>1437-7772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU1Lw0AQhhdRbK1e_AGyIHgQorObZKc5luInBT3oOUw2G5uaZONuivTfu6WFgqd5Bx4ehnkZuxRwJwDw_n0BAEJCJo_YWCQxRogoj0OOExFlSqYjdub9KkCoUnnKRkIgKMRszPzMe6trGmrbcVvx3jab1rp-WfvW87rjw9LwwgwUSU5duYsxp9KZzmrTD9bxL9MZz3_rYcld7b-3Gm0b64weqOGaOm3cVvVKPQXSnLOTihpvLvZzwj4fHz7mz9Hi7ellPltEWmI2RIQFpaUQmSpjWRktplWZakBMCFRZTUUBFdA2kEEsMkpUEZaUEqEo0RBP2M3O2zv7szZ-yNvaa9M04Qq79jlKiUomGMDrf-DKrl0XbstFGkMCUwUyULc7SjvrvTNV3ru6JbfJBeTbIvJDEQG-2ivXRWvKA7r_fPwH5CqDDg</recordid><startdate>200106</startdate><enddate>200106</enddate><creator>Takezaki, T</creator><creator>Hamajima, N</creator><creator>Matsuo, K</creator><creator>Tanaka, R</creator><creator>Hirai, T</creator><creator>Kato, T</creator><creator>Ohashi, K</creator><creator>Tajima, K</creator><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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200106</creationdate><title>Association of polymorphisms in the beta-2 and beta-3 adrenoceptor genes with risk of colorectal cancer in Japanese</title><author>Takezaki, T ; Hamajima, N ; Matsuo, K ; Tanaka, R ; Hirai, T ; Kato, T ; Ohashi, K ; Tajima, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c279t-a7ba5d1196d32fec18fd5c0774a06df81b0f0adf81ae77b9a46bf815a416a4c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Body Mass Index</topic><topic>Case-Control Studies</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - ethnology</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Confidence intervals</topic><topic>DNA, Neoplasm - genetics</topic><topic>Female</topic><topic>Genes</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Insulin Resistance</topic><topic>Japan - epidemiology</topic><topic>Japan - ethnology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Obesity</topic><topic>Polymorphism, Genetic</topic><topic>Receptors, Adrenergic, beta-2 - genetics</topic><topic>Receptors, Adrenergic, beta-3 - genetics</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takezaki, T</creatorcontrib><creatorcontrib>Hamajima, N</creatorcontrib><creatorcontrib>Matsuo, K</creatorcontrib><creatorcontrib>Tanaka, R</creatorcontrib><creatorcontrib>Hirai, T</creatorcontrib><creatorcontrib>Kato, T</creatorcontrib><creatorcontrib>Ohashi, K</creatorcontrib><creatorcontrib>Tajima, K</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>Oncogenes and Growth Factors Abstracts</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>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest_Research Library</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takezaki, T</au><au>Hamajima, N</au><au>Matsuo, K</au><au>Tanaka, R</au><au>Hirai, T</au><au>Kato, T</au><au>Ohashi, K</au><au>Tajima, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of polymorphisms in the beta-2 and beta-3 adrenoceptor genes with risk of colorectal cancer in Japanese</atitle><jtitle>International journal of clinical oncology</jtitle><addtitle>Int J Clin Oncol</addtitle><date>2001-06</date><risdate>2001</risdate><volume>6</volume><issue>3</issue><spage>117</spage><epage>122</epage><pages>117-122</pages><issn>1341-9625</issn><eissn>1437-7772</eissn><abstract>The adrenergic receptor system is involved in thermogenesis and in the activation of lipid mobilization in fat cells, and polymorphisms in the beta-2 and beta-3 adrenoceptor genes (BAR2 and BAR3) have been reported to be associated with obesity and insulin resistance. To examine links between polymorphisms in these genes and the risk of colorectal cancer in Japanese, we conducted the present hospital-based case-referent study.
Mutations of the BAR2 gene at codon 27 (Gln27Glu) and of the BAR3 gene at codon 64 (Trp64Arg) were examined in 131 patients with colorectal cancer (cases) and in 239 cancer-free referents. We also collected information on environmental factors, using a questionnaire approach. Odds ratios (ORs) were estimated with an unconditional logistic model, after adjustment for potential confounding factors.
The proportional distribution of the mutations in BAR2 and BAR3 did not differ between cases and referents. Analysis of a subgroup with a higher body mass index showed that the Trp64Arg variant increased the OR (2.63; 95% confidence interval, 1.13-6.11) for colon cancer, but not for rectal cancer, compared with the Trp64 genotype. Altered ORs for colon and rectal cancers with the Gln27Glu variant were not observed in either the subgroup with the lower body mass index or the subgroup with the higher body mass index.
These findings suggest that the BAR3 polymorphism may alter the susceptibility to colon cancer risk in obese subjects. To confirm this finding, a further study with a larger number of subjects is now required.</abstract><cop>Japan</cop><pub>Springer Nature B.V</pub><pmid>11706779</pmid><doi>10.1007/PL00012092</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Body Mass Index Case-Control Studies Colorectal cancer Colorectal Neoplasms - ethnology Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology Confidence intervals DNA, Neoplasm - genetics Female Genes Genetic Predisposition to Disease Humans Insulin Resistance Japan - epidemiology Japan - ethnology Male Middle Aged Mutation Obesity Polymorphism, Genetic Receptors, Adrenergic, beta-2 - genetics Receptors, Adrenergic, beta-3 - genetics Risk Factors |
title | Association of polymorphisms in the beta-2 and beta-3 adrenoceptor genes with risk of colorectal cancer in Japanese |
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