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Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder
Bladder carcinoma is the most common malignancy of the urinary tract. The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with transitional cell carcinoma and 27 controls were recru...
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Published in: | Oncology letters 2016-10, Vol.12 (4), p.2872-2879 |
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container_title | Oncology letters |
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creator | Avcilar, Tuba Kirac, Deniz Ergec, Deniz Koc, Gulsah Ulucan, Korkut Kaya, Zehra Kaspar, Elif Cigdem Turkeri, Levent Guney, Ahmet Ilter |
description | Bladder carcinoma is the most common malignancy of the urinary tract. The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with transitional cell carcinoma and 27 controls were recruited for the study. Bladder cancer tissues were obtained by radical cystectomy or transurethral resection. Genomic DNA was extracted from peripheral blood. mtDNA and p53 genes were amplified by polymerase chain reaction and sequenced directly. A total of 37 polymorphisms were identified, among which, 2 mutations were significant in the patient group, and 1 mutation was significant in the control group. Additionally, 5 different moderate positive correlations between mtDNA mutations and 3 different positive correlations between p53 gene and mtDNA mutations were detected. The high incidence of mtDNA and p53 gene mutations in bladder cancer suggests that these genes could be important in carcinogenesis. |
doi_str_mv | 10.3892/ol.2016.5000 |
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The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with transitional cell carcinoma and 27 controls were recruited for the study. Bladder cancer tissues were obtained by radical cystectomy or transurethral resection. Genomic DNA was extracted from peripheral blood. mtDNA and p53 genes were amplified by polymerase chain reaction and sequenced directly. A total of 37 polymorphisms were identified, among which, 2 mutations were significant in the patient group, and 1 mutation was significant in the control group. Additionally, 5 different moderate positive correlations between mtDNA mutations and 3 different positive correlations between p53 gene and mtDNA mutations were detected. 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Spandidos</publisher><subject>Bladder cancer ; bladder carcinoma ; Cell cycle ; Cytochrome ; Dehydrogenases ; Deoxyribonucleic acid ; Development and progression ; DNA ; DNA polymerase ; Gene expression ; Gene mutation ; Genes ; Genetic aspects ; Genetic testing ; Health aspects ; Medical research ; Mitochondrial DNA ; mtDNA ; Mutation ; Oncology ; p53 ; TCC ; Tumors</subject><ispartof>Oncology letters, 2016-10, Vol.12 (4), p.2872-2879</ispartof><rights>Copyright © 2016, Spandidos Publications</rights><rights>COPYRIGHT 2016 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2016</rights><rights>Copyright © 2016, Spandidos Publications 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-e32cde20c63bf298ec5bd41f98668febf129abc5b9705bb85294dd1df879be4b3</citedby><cites>FETCH-LOGICAL-c539t-e32cde20c63bf298ec5bd41f98668febf129abc5b9705bb85294dd1df879be4b3</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/PMC5038862/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038862/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27698873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Avcilar, Tuba</creatorcontrib><creatorcontrib>Kirac, Deniz</creatorcontrib><creatorcontrib>Ergec, Deniz</creatorcontrib><creatorcontrib>Koc, Gulsah</creatorcontrib><creatorcontrib>Ulucan, Korkut</creatorcontrib><creatorcontrib>Kaya, Zehra</creatorcontrib><creatorcontrib>Kaspar, Elif Cigdem</creatorcontrib><creatorcontrib>Turkeri, Levent</creatorcontrib><creatorcontrib>Guney, Ahmet Ilter</creatorcontrib><title>Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Bladder carcinoma is the most common malignancy of the urinary tract. The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with transitional cell carcinoma and 27 controls were recruited for the study. Bladder cancer tissues were obtained by radical cystectomy or transurethral resection. Genomic DNA was extracted from peripheral blood. mtDNA and p53 genes were amplified by polymerase chain reaction and sequenced directly. A total of 37 polymorphisms were identified, among which, 2 mutations were significant in the patient group, and 1 mutation was significant in the control group. Additionally, 5 different moderate positive correlations between mtDNA mutations and 3 different positive correlations between p53 gene and mtDNA mutations were detected. The high incidence of mtDNA and p53 gene mutations in bladder cancer suggests that these genes could be important in carcinogenesis.</description><subject>Bladder cancer</subject><subject>bladder carcinoma</subject><subject>Cell cycle</subject><subject>Cytochrome</subject><subject>Dehydrogenases</subject><subject>Deoxyribonucleic acid</subject><subject>Development and progression</subject><subject>DNA</subject><subject>DNA polymerase</subject><subject>Gene expression</subject><subject>Gene mutation</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic testing</subject><subject>Health aspects</subject><subject>Medical research</subject><subject>Mitochondrial DNA</subject><subject>mtDNA</subject><subject>Mutation</subject><subject>Oncology</subject><subject>p53</subject><subject>TCC</subject><subject>Tumors</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNptkktr3DAUhU1paUKaXddF0FK66Ez1sGxpExiSPgJDs2nXQo_rGQVbmlp2Slf965FnEpMpRWBJ1989so5PUbwmeMmEpJ9iu6SYVEuOMX5WnJJa0gXBgj6f13V5UpyndJsBzCsiRPWyOKF1JYWo2Wnx9zrcQRr8Rg8-BhQbNGwB6ZSi9YeSgeE3QECdH6LdxuB6r1t09X2FdHBoxxnaQADUjcOeT8gHNPQ6JD9tM2qhzQ_dWx9ipx-PMK12DvpXxYtGtwnOH-az4ueXzz8uvy3WN1-vL1frheVMDgtg1Dqg2FbMNFQKsNy4kjRSVJVowDSESm1yUdaYGyM4laVzxDWilgZKw86Ki4PubjQdOAshf2Ordr3vdP9HRe3V8Zvgt2oT7xTHLHtGs8CHB4E-_hqzZarzabqaDhDHpIhgnHEsS5LRt_-gt3HssxWZkoxWXIo8z9RGt6B8aGI-106ialXmW5VVKSat5X-oPBx03sYAjc_1o4b3Txq2oNthm2I77v_NMfjxANo-ptRDM5tBsJrCpWKrpnCpKVwZf_PUwBl-jFIG3h2AtMvB8C6mmblZL3Aee517ivnWcA</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Avcilar, Tuba</creator><creator>Kirac, Deniz</creator><creator>Ergec, Deniz</creator><creator>Koc, Gulsah</creator><creator>Ulucan, Korkut</creator><creator>Kaya, Zehra</creator><creator>Kaspar, Elif Cigdem</creator><creator>Turkeri, Levent</creator><creator>Guney, Ahmet Ilter</creator><general>D.A. Spandidos</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161001</creationdate><title>Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder</title><author>Avcilar, Tuba ; Kirac, Deniz ; Ergec, Deniz ; Koc, Gulsah ; Ulucan, Korkut ; Kaya, Zehra ; Kaspar, Elif Cigdem ; Turkeri, Levent ; Guney, Ahmet Ilter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-e32cde20c63bf298ec5bd41f98668febf129abc5b9705bb85294dd1df879be4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bladder cancer</topic><topic>bladder carcinoma</topic><topic>Cell cycle</topic><topic>Cytochrome</topic><topic>Dehydrogenases</topic><topic>Deoxyribonucleic acid</topic><topic>Development and progression</topic><topic>DNA</topic><topic>DNA polymerase</topic><topic>Gene expression</topic><topic>Gene mutation</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic testing</topic><topic>Health aspects</topic><topic>Medical research</topic><topic>Mitochondrial DNA</topic><topic>mtDNA</topic><topic>Mutation</topic><topic>Oncology</topic><topic>p53</topic><topic>TCC</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Avcilar, Tuba</creatorcontrib><creatorcontrib>Kirac, Deniz</creatorcontrib><creatorcontrib>Ergec, Deniz</creatorcontrib><creatorcontrib>Koc, Gulsah</creatorcontrib><creatorcontrib>Ulucan, Korkut</creatorcontrib><creatorcontrib>Kaya, Zehra</creatorcontrib><creatorcontrib>Kaspar, Elif Cigdem</creatorcontrib><creatorcontrib>Turkeri, Levent</creatorcontrib><creatorcontrib>Guney, Ahmet Ilter</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Avcilar, Tuba</au><au>Kirac, Deniz</au><au>Ergec, Deniz</au><au>Koc, Gulsah</au><au>Ulucan, Korkut</au><au>Kaya, Zehra</au><au>Kaspar, Elif Cigdem</au><au>Turkeri, Levent</au><au>Guney, Ahmet Ilter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2016-10-01</date><risdate>2016</risdate><volume>12</volume><issue>4</issue><spage>2872</spage><epage>2879</epage><pages>2872-2879</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>Bladder carcinoma is the most common malignancy of the urinary tract. The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with transitional cell carcinoma and 27 controls were recruited for the study. Bladder cancer tissues were obtained by radical cystectomy or transurethral resection. Genomic DNA was extracted from peripheral blood. mtDNA and p53 genes were amplified by polymerase chain reaction and sequenced directly. A total of 37 polymorphisms were identified, among which, 2 mutations were significant in the patient group, and 1 mutation was significant in the control group. Additionally, 5 different moderate positive correlations between mtDNA mutations and 3 different positive correlations between p53 gene and mtDNA mutations were detected. The high incidence of mtDNA and p53 gene mutations in bladder cancer suggests that these genes could be important in carcinogenesis.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>27698873</pmid><doi>10.3892/ol.2016.5000</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bladder cancer bladder carcinoma Cell cycle Cytochrome Dehydrogenases Deoxyribonucleic acid Development and progression DNA DNA polymerase Gene expression Gene mutation Genes Genetic aspects Genetic testing Health aspects Medical research Mitochondrial DNA mtDNA Mutation Oncology p53 TCC Tumors |
title | Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder |
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