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Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome
BACKGROUND: Cervical cancer (CC), a leading cause of cancer-related deaths in women worldwide, has been causally linked to genital human papillomavirus (HPV) infection. Although a host of genetic alterations have been identified, molecular basis of CC development is still poorly understood. RESULTS:...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156646/ https://www.ncbi.nlm.nih.gov/pubmed/12773202 http://dx.doi.org/10.1186/1476-4598-2-24 |
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author | Narayan, Gopeshwar Arias-Pulido, Hugo Koul, Sanjay Vargas, Hernan Zhang, Fang F Villella, Jeannine Schneider, Achim Terry, Mary B Mansukhani, Mahesh Murty, Vundavalli V |
author_facet | Narayan, Gopeshwar Arias-Pulido, Hugo Koul, Sanjay Vargas, Hernan Zhang, Fang F Villella, Jeannine Schneider, Achim Terry, Mary B Mansukhani, Mahesh Murty, Vundavalli V |
author_sort | Narayan, Gopeshwar |
collection | PubMed |
description | BACKGROUND: Cervical cancer (CC), a leading cause of cancer-related deaths in women worldwide, has been causally linked to genital human papillomavirus (HPV) infection. Although a host of genetic alterations have been identified, molecular basis of CC development is still poorly understood. RESULTS: We examined the role of promoter hypermethylation, an epigenetic alteration that is associated with the silencing tumor suppressor genes in human cancer, by studying 16 gene promoters in 90 CC cases. We found a high frequency of promoter methylation in CDH1, DAPK, RARB, and HIC1 genes. Correlation of promoter methylation with clinical characteristics and other genetic changes revealed the following: a) overall promoter methylation was higher in more advanced stage of the disease, b) promoter methylation of RARB and BRCA1 predicted worse prognosis, and c) the HIC1 promoter methylation was frequently seen in association with microsatellite instability. Promoter methylation was associated with gene silencing in CC cell lines. Treatment with methylation or histone deacetylation-inhibiting agents resulted in profound reactivation of gene expression. CONCLUSIONS: These results may have implications in understanding the underlying epigenetic mechanisms in CC development, provide prognostic indicators, and identify important gene targets for treatment. |
format | Text |
id | pubmed-156646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1566462003-06-05 Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome Narayan, Gopeshwar Arias-Pulido, Hugo Koul, Sanjay Vargas, Hernan Zhang, Fang F Villella, Jeannine Schneider, Achim Terry, Mary B Mansukhani, Mahesh Murty, Vundavalli V Mol Cancer Research BACKGROUND: Cervical cancer (CC), a leading cause of cancer-related deaths in women worldwide, has been causally linked to genital human papillomavirus (HPV) infection. Although a host of genetic alterations have been identified, molecular basis of CC development is still poorly understood. RESULTS: We examined the role of promoter hypermethylation, an epigenetic alteration that is associated with the silencing tumor suppressor genes in human cancer, by studying 16 gene promoters in 90 CC cases. We found a high frequency of promoter methylation in CDH1, DAPK, RARB, and HIC1 genes. Correlation of promoter methylation with clinical characteristics and other genetic changes revealed the following: a) overall promoter methylation was higher in more advanced stage of the disease, b) promoter methylation of RARB and BRCA1 predicted worse prognosis, and c) the HIC1 promoter methylation was frequently seen in association with microsatellite instability. Promoter methylation was associated with gene silencing in CC cell lines. Treatment with methylation or histone deacetylation-inhibiting agents resulted in profound reactivation of gene expression. CONCLUSIONS: These results may have implications in understanding the underlying epigenetic mechanisms in CC development, provide prognostic indicators, and identify important gene targets for treatment. BioMed Central 2003-05-13 /pmc/articles/PMC156646/ /pubmed/12773202 http://dx.doi.org/10.1186/1476-4598-2-24 Text en Copyright © 2003 Narayan et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Narayan, Gopeshwar Arias-Pulido, Hugo Koul, Sanjay Vargas, Hernan Zhang, Fang F Villella, Jeannine Schneider, Achim Terry, Mary B Mansukhani, Mahesh Murty, Vundavalli V Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome |
title | Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome |
title_full | Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome |
title_fullStr | Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome |
title_full_unstemmed | Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome |
title_short | Frequent Promoter Methylation of CDH1, DAPK, RARB, and HIC1 Genes in Carcinoma of Cervix Uteri: Its Relationship to Clinical Outcome |
title_sort | frequent promoter methylation of cdh1, dapk, rarb, and hic1 genes in carcinoma of cervix uteri: its relationship to clinical outcome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156646/ https://www.ncbi.nlm.nih.gov/pubmed/12773202 http://dx.doi.org/10.1186/1476-4598-2-24 |
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