CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer

<p>Abstract</p> <p>Background</p> <p>Gene silencing associated with aberrant methylation of promoter region CpG islands is an acquired epigenetic alteration that serves as an alternative to genetic defects in the inactivation of tumor suppressor and other genes in human...

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Main Authors: Tamandani DM, Sobti RC, Shekari M, Huria A
Format: Article
Language:English
Published: BMC 2009-02-01
Series:European Journal of Medical Research
Subjects:
Online Access:http://www.eurjmedres.com/content/14/2/71
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spelling doaj-5d6d596b5ac945489dd87dd658fab4772020-11-24T21:23:49ZengBMCEuropean Journal of Medical Research2047-783X2009-02-011427110.1186/2047-783X-14-2-71CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancerTamandani DMSobti RCShekari MHuria A<p>Abstract</p> <p>Background</p> <p>Gene silencing associated with aberrant methylation of promoter region CpG islands is an acquired epigenetic alteration that serves as an alternative to genetic defects in the inactivation of tumor suppressor and other genes in human cancers.</p> <p>Aims</p> <p>This study describes the methylation status of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer. We also examined the prevalence of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes methylation in cervical cancer tissue and none - neo plastic samples in an effort to correlate with smoking habit and clinicopathological features.</p> <p>Method</p> <p>Target DNA was modified by sodium bisulfite, converting all unmethylated, but not methylated, cytosines to uracil, and subsequently amplified by Methylation Specific (MS) PCR with primers specific for methylated versus unmethylated DNA. The PCR product was detected by gel electrophoresis and combined with the clinical records of patients.</p> <p>Results</p> <p>The methylation pattern of the <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in specimens of cervical cancer and adjacent normal tissues were detected [5/80 (6.2%), 3/80 (3.75%)-2/80 (2.5%), 1/80 (1.2%) respectively]. No statistical differences were seen in the extent of differentiation, invasion, pathological type and smoking habit between the methylated and unmethylated tissues (<it>P </it>> 0.05).</p> <p>Conclusion</p> <p>The present study conclude that the frequency of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes methylation in cervical cancer are rare (< 6%), and have no any critical role in development of cervical cancer.</p> http://www.eurjmedres.com/content/14/2/71Methylation<it>TMS1</it>/<it>ASC</it><it>CASP8</it>cervical cancer
collection DOAJ
language English
format Article
sources DOAJ
author Tamandani DM
Sobti RC
Shekari M
Huria A
spellingShingle Tamandani DM
Sobti RC
Shekari M
Huria A
CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer
European Journal of Medical Research
Methylation
<it>TMS1</it>/<it>ASC</it>
<it>CASP8</it>
cervical cancer
author_facet Tamandani DM
Sobti RC
Shekari M
Huria A
author_sort Tamandani DM
title CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer
title_short CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer
title_full CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer
title_fullStr CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer
title_full_unstemmed CpG island methylation of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer
title_sort cpg island methylation of <it>tms1</it>/<it>asc </it>and <it>casp8 </it>genes in cervical cancer
publisher BMC
series European Journal of Medical Research
issn 2047-783X
publishDate 2009-02-01
description <p>Abstract</p> <p>Background</p> <p>Gene silencing associated with aberrant methylation of promoter region CpG islands is an acquired epigenetic alteration that serves as an alternative to genetic defects in the inactivation of tumor suppressor and other genes in human cancers.</p> <p>Aims</p> <p>This study describes the methylation status of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in cervical cancer. We also examined the prevalence of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes methylation in cervical cancer tissue and none - neo plastic samples in an effort to correlate with smoking habit and clinicopathological features.</p> <p>Method</p> <p>Target DNA was modified by sodium bisulfite, converting all unmethylated, but not methylated, cytosines to uracil, and subsequently amplified by Methylation Specific (MS) PCR with primers specific for methylated versus unmethylated DNA. The PCR product was detected by gel electrophoresis and combined with the clinical records of patients.</p> <p>Results</p> <p>The methylation pattern of the <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes in specimens of cervical cancer and adjacent normal tissues were detected [5/80 (6.2%), 3/80 (3.75%)-2/80 (2.5%), 1/80 (1.2%) respectively]. No statistical differences were seen in the extent of differentiation, invasion, pathological type and smoking habit between the methylated and unmethylated tissues (<it>P </it>> 0.05).</p> <p>Conclusion</p> <p>The present study conclude that the frequency of <it>TMS1</it>/<it>ASC </it>and <it>CASP8 </it>genes methylation in cervical cancer are rare (< 6%), and have no any critical role in development of cervical cancer.</p>
topic Methylation
<it>TMS1</it>/<it>ASC</it>
<it>CASP8</it>
cervical cancer
url http://www.eurjmedres.com/content/14/2/71
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