Cargando…

Hypermethylation of tumor-related genes in genitourinary cancer cell lines.

Hypermethylation of CpG island is a common mechanism for the inactivation of tumor-related genes. In the present study, we analyzed 13 genitourinary cancer cell lines for aberrant DNA methylation of 5 tumor-related genes using methylation- specific polymerase chain reaction (MSP). GSTP1 was methylat...

Descripción completa

Detalles Bibliográficos
Autores principales: Chung, W. B., Hong, S. H., Kim, J. A., Sohn, Y. K., Kim, B. W., Kim, J. W.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054792/
https://www.ncbi.nlm.nih.gov/pubmed/11748358
_version_ 1782200032056836096
author Chung, W. B.
Hong, S. H.
Kim, J. A.
Sohn, Y. K.
Kim, B. W.
Kim, J. W.
author_facet Chung, W. B.
Hong, S. H.
Kim, J. A.
Sohn, Y. K.
Kim, B. W.
Kim, J. W.
author_sort Chung, W. B.
collection PubMed
description Hypermethylation of CpG island is a common mechanism for the inactivation of tumor-related genes. In the present study, we analyzed 13 genitourinary cancer cell lines for aberrant DNA methylation of 5 tumor-related genes using methylation- specific polymerase chain reaction (MSP). GSTP1 was methylated in 5 (38.5%), E-cadherin in 1 (8%), VHL in 1 (8%), and MGMT and hMLH1 in none (0%). Six out of thirteen genitourinary cancer cell lines had methylation of at least one of five genes; 5 had one gene methylated, and, 1 had two genes methylated. Methylation of these 5 genes was not detected in any of the bladder cancer cell lines. GSTP1 was methylated in all of the 3 prostate cancer cell lines. We conclude that aberrant hypermethylation may be an important mechanism for the inactivation of cancer-related genes in kidney and prostate cancer cell lines.
format Text
id pubmed-3054792
institution National Center for Biotechnology Information
language English
publishDate 2001
publisher Korean Academy of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-30547922011-03-15 Hypermethylation of tumor-related genes in genitourinary cancer cell lines. Chung, W. B. Hong, S. H. Kim, J. A. Sohn, Y. K. Kim, B. W. Kim, J. W. J Korean Med Sci Research Article Hypermethylation of CpG island is a common mechanism for the inactivation of tumor-related genes. In the present study, we analyzed 13 genitourinary cancer cell lines for aberrant DNA methylation of 5 tumor-related genes using methylation- specific polymerase chain reaction (MSP). GSTP1 was methylated in 5 (38.5%), E-cadherin in 1 (8%), VHL in 1 (8%), and MGMT and hMLH1 in none (0%). Six out of thirteen genitourinary cancer cell lines had methylation of at least one of five genes; 5 had one gene methylated, and, 1 had two genes methylated. Methylation of these 5 genes was not detected in any of the bladder cancer cell lines. GSTP1 was methylated in all of the 3 prostate cancer cell lines. We conclude that aberrant hypermethylation may be an important mechanism for the inactivation of cancer-related genes in kidney and prostate cancer cell lines. Korean Academy of Medical Sciences 2001-12 /pmc/articles/PMC3054792/ /pubmed/11748358 Text en
spellingShingle Research Article
Chung, W. B.
Hong, S. H.
Kim, J. A.
Sohn, Y. K.
Kim, B. W.
Kim, J. W.
Hypermethylation of tumor-related genes in genitourinary cancer cell lines.
title Hypermethylation of tumor-related genes in genitourinary cancer cell lines.
title_full Hypermethylation of tumor-related genes in genitourinary cancer cell lines.
title_fullStr Hypermethylation of tumor-related genes in genitourinary cancer cell lines.
title_full_unstemmed Hypermethylation of tumor-related genes in genitourinary cancer cell lines.
title_short Hypermethylation of tumor-related genes in genitourinary cancer cell lines.
title_sort hypermethylation of tumor-related genes in genitourinary cancer cell lines.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054792/
https://www.ncbi.nlm.nih.gov/pubmed/11748358
work_keys_str_mv AT chungwb hypermethylationoftumorrelatedgenesingenitourinarycancercelllines
AT hongsh hypermethylationoftumorrelatedgenesingenitourinarycancercelllines
AT kimja hypermethylationoftumorrelatedgenesingenitourinarycancercelllines
AT sohnyk hypermethylationoftumorrelatedgenesingenitourinarycancercelllines
AT kimbw hypermethylationoftumorrelatedgenesingenitourinarycancercelllines
AT kimjw hypermethylationoftumorrelatedgenesingenitourinarycancercelllines