Association of the vascular endothelial growth factor -2578C/A polymorphism with cancer risk: A meta-analysis update
The vascular endothelial growth factor (VEGF) -2578C/A polymorphism has been previously reported to be associated with cancer risk; however, the results have been controversial. Therefore, the aim of the present study was to explore the association between the VEGF -2578C/A polymorphism with the can...
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Veröffentlicht in: | Biomedical reports 2014-11, Vol.2 (6), p.823-830 |
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description | The vascular endothelial growth factor (VEGF) -2578C/A polymorphism has been previously reported to be associated with cancer risk; however, the results have been controversial. Therefore, the aim of the present study was to explore the association between the VEGF -2578C/A polymorphism with the cancer risk. A total of 37 case-control studies were identified. The pooled analysis showed that there was no association between VEGF -2578C/A and the risk of cancer, and the odds ratios (ORs) [with the corresponding 95% confidence intervals (95% CIs)] were 0.97 (0.91-1.04) for C vs. A, 0.94 (0.86-1.02) for CC vs. AA, 0.92 (0.80-1.06) for CA vs. AA, 0.96 (0.89-1.03) for CC/CA vs. AA and 0.97 (0.88-1.08) for CC vs. CA/AA. Subgroup analyses according to ethnicity, source of control and type of cancer showed that the VEGF -2578C/A polymorphism is associated with colorectal and lung cancers. Additionally, the polymorphism may decrease the risk of cancer in the Asian population. This VEGF polymorphism was not associated with a risk of cancer for the Caucasian [0.92 (0.76-1.11) for CC vs. AA] and African populations [1.31 (0.67-2.58) for CC vs. AA], and it was not associated with bladder [1.06 (0.74-1.53) for CC/AA] and breast cancers [1.01 (0.90-1.15) for CC/AA]. Therefore, the present meta-analysis indicates that VEGF -2578C/A may only be associated with the risk of colorectal cancer, lung cancer and the Asian population. More studies with larger sample sizes are required to provide more conclusive evidence. |
doi_str_mv | 10.3892/br.2014.317 |
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Therefore, the aim of the present study was to explore the association between the VEGF -2578C/A polymorphism with the cancer risk. A total of 37 case-control studies were identified. The pooled analysis showed that there was no association between VEGF -2578C/A and the risk of cancer, and the odds ratios (ORs) [with the corresponding 95% confidence intervals (95% CIs)] were 0.97 (0.91-1.04) for C vs. A, 0.94 (0.86-1.02) for CC vs. AA, 0.92 (0.80-1.06) for CA vs. AA, 0.96 (0.89-1.03) for CC/CA vs. AA and 0.97 (0.88-1.08) for CC vs. CA/AA. Subgroup analyses according to ethnicity, source of control and type of cancer showed that the VEGF -2578C/A polymorphism is associated with colorectal and lung cancers. Additionally, the polymorphism may decrease the risk of cancer in the Asian population. This VEGF polymorphism was not associated with a risk of cancer for the Caucasian [0.92 (0.76-1.11) for CC vs. AA] and African populations [1.31 (0.67-2.58) for CC vs. AA], and it was not associated with bladder [1.06 (0.74-1.53) for CC/AA] and breast cancers [1.01 (0.90-1.15) for CC/AA]. Therefore, the present meta-analysis indicates that VEGF -2578C/A may only be associated with the risk of colorectal cancer, lung cancer and the Asian population. More studies with larger sample sizes are required to provide more conclusive evidence.</description><identifier>ISSN: 2049-9434</identifier><identifier>EISSN: 2049-9442</identifier><identifier>DOI: 10.3892/br.2014.317</identifier><identifier>PMID: 25279153</identifier><language>eng</language><publisher>England: D.A. Spandidos</publisher><subject>Angiogenesis ; Bladder ; Breast ; Breast cancer ; Cancer ; cancer susceptibility ; Colorectal cancer ; Colorectal carcinoma ; Confidence intervals ; Ethnicity ; Genetic aspects ; Genetic polymorphisms ; Health aspects ; Lung cancer ; Meta-analysis ; Metastasis ; Minority & ethnic groups ; Physiological aspects ; Polymorphism ; Population studies ; Prostate ; Risk analysis ; Risk factors ; Studies ; Urinary bladder ; Vascular endothelial growth factor ; White people</subject><ispartof>Biomedical reports, 2014-11, Vol.2 (6), p.823-830</ispartof><rights>Copyright © 2014, Spandidos Publications</rights><rights>COPYRIGHT 2014 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2014</rights><rights>Copyright © 2014, Spandidos Publications 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-6fc0365cff2ea9a05cd1ee7e0616d649b44b64e77231b93f1501ae49e397aeaf3</citedby><cites>FETCH-LOGICAL-c437t-6fc0365cff2ea9a05cd1ee7e0616d649b44b64e77231b93f1501ae49e397aeaf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179765/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179765/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,5556,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25279153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHEN, QUANCHI</creatorcontrib><creatorcontrib>ZHOU, ZIFEI</creatorcontrib><creatorcontrib>SHAN, LIANGCHENG</creatorcontrib><creatorcontrib>HUA, YINGQI</creatorcontrib><creatorcontrib>ZENG, HUI</creatorcontrib><creatorcontrib>LIU, PENGCHENG</creatorcontrib><creatorcontrib>CAI, ZHENGDONG</creatorcontrib><title>Association of the vascular endothelial growth factor -2578C/A polymorphism with cancer risk: A meta-analysis update</title><title>Biomedical reports</title><addtitle>Biomed Rep</addtitle><description>The vascular endothelial growth factor (VEGF) -2578C/A polymorphism has been previously reported to be associated with cancer risk; however, the results have been controversial. Therefore, the aim of the present study was to explore the association between the VEGF -2578C/A polymorphism with the cancer risk. A total of 37 case-control studies were identified. The pooled analysis showed that there was no association between VEGF -2578C/A and the risk of cancer, and the odds ratios (ORs) [with the corresponding 95% confidence intervals (95% CIs)] were 0.97 (0.91-1.04) for C vs. A, 0.94 (0.86-1.02) for CC vs. AA, 0.92 (0.80-1.06) for CA vs. AA, 0.96 (0.89-1.03) for CC/CA vs. AA and 0.97 (0.88-1.08) for CC vs. CA/AA. Subgroup analyses according to ethnicity, source of control and type of cancer showed that the VEGF -2578C/A polymorphism is associated with colorectal and lung cancers. Additionally, the polymorphism may decrease the risk of cancer in the Asian population. This VEGF polymorphism was not associated with a risk of cancer for the Caucasian [0.92 (0.76-1.11) for CC vs. AA] and African populations [1.31 (0.67-2.58) for CC vs. AA], and it was not associated with bladder [1.06 (0.74-1.53) for CC/AA] and breast cancers [1.01 (0.90-1.15) for CC/AA]. Therefore, the present meta-analysis indicates that VEGF -2578C/A may only be associated with the risk of colorectal cancer, lung cancer and the Asian population. More studies with larger sample sizes are required to provide more conclusive evidence.</description><subject>Angiogenesis</subject><subject>Bladder</subject><subject>Breast</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>cancer susceptibility</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Confidence intervals</subject><subject>Ethnicity</subject><subject>Genetic aspects</subject><subject>Genetic polymorphisms</subject><subject>Health aspects</subject><subject>Lung cancer</subject><subject>Meta-analysis</subject><subject>Metastasis</subject><subject>Minority & ethnic groups</subject><subject>Physiological aspects</subject><subject>Polymorphism</subject><subject>Population studies</subject><subject>Prostate</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Studies</subject><subject>Urinary bladder</subject><subject>Vascular endothelial growth factor</subject><subject>White people</subject><issn>2049-9434</issn><issn>2049-9442</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkt2L1DAUxYso7rLuk-8SEESQzuarTePDwjD4BQu-6HO4TW9msrZNTdpd5r83w6yjKyYPudz87gknnKJ4yehKNJpftXHFKZMrwdST4pxTqUstJX96qoU8Ky5TuqV5aUV51TwvznjFlWaVOC_mdUrBeph9GElwZN4huYNklx4iwbELudF76Mk2hvt5RxzYOURS8ko1m6s1mUK_H0Kcdj4N5N5nwsJoMZLo04_3ZE0GnKGEEfp98oksUwczviieOegTXj6cF8X3jx--bT6XN18_fdmsb0orhZrL2lkq6so6xxE00Mp2DFEhrVnd1VK3Ura1RKW4YK0WjlWUAUqNQitAcOKiuD7qTks7YGdxnCP0Zop-gLg3Abx5fDP6ndmGOyOZ0qqussDbB4EYfi6YZjP4ZLHvYcSwJMMaXtesYlxk9PU_6G1YYvadKS2o5loI-YfaQo_Gjy7kd-1B1KwlZaKhTDeZWv2HyrvDwdswovO5_2jg3XHAxpBSRHfyyKg55MS00RxyYnJOMv3q7285sb9TkYE3RyBNMHa-C-nEtLGkvKR1SZts-hfj1sQ1</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>CHEN, QUANCHI</creator><creator>ZHOU, ZIFEI</creator><creator>SHAN, LIANGCHENG</creator><creator>HUA, YINGQI</creator><creator>ZENG, HUI</creator><creator>LIU, PENGCHENG</creator><creator>CAI, ZHENGDONG</creator><general>D.A. 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Therefore, the aim of the present study was to explore the association between the VEGF -2578C/A polymorphism with the cancer risk. A total of 37 case-control studies were identified. The pooled analysis showed that there was no association between VEGF -2578C/A and the risk of cancer, and the odds ratios (ORs) [with the corresponding 95% confidence intervals (95% CIs)] were 0.97 (0.91-1.04) for C vs. A, 0.94 (0.86-1.02) for CC vs. AA, 0.92 (0.80-1.06) for CA vs. AA, 0.96 (0.89-1.03) for CC/CA vs. AA and 0.97 (0.88-1.08) for CC vs. CA/AA. Subgroup analyses according to ethnicity, source of control and type of cancer showed that the VEGF -2578C/A polymorphism is associated with colorectal and lung cancers. Additionally, the polymorphism may decrease the risk of cancer in the Asian population. This VEGF polymorphism was not associated with a risk of cancer for the Caucasian [0.92 (0.76-1.11) for CC vs. AA] and African populations [1.31 (0.67-2.58) for CC vs. AA], and it was not associated with bladder [1.06 (0.74-1.53) for CC/AA] and breast cancers [1.01 (0.90-1.15) for CC/AA]. Therefore, the present meta-analysis indicates that VEGF -2578C/A may only be associated with the risk of colorectal cancer, lung cancer and the Asian population. More studies with larger sample sizes are required to provide more conclusive evidence.</abstract><cop>England</cop><pub>D.A. Spandidos</pub><pmid>25279153</pmid><doi>10.3892/br.2014.317</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Bladder Breast Breast cancer Cancer cancer susceptibility Colorectal cancer Colorectal carcinoma Confidence intervals Ethnicity Genetic aspects Genetic polymorphisms Health aspects Lung cancer Meta-analysis Metastasis Minority & ethnic groups Physiological aspects Polymorphism Population studies Prostate Risk analysis Risk factors Studies Urinary bladder Vascular endothelial growth factor White people |
title | Association of the vascular endothelial growth factor -2578C/A polymorphism with cancer risk: A meta-analysis update |
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