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Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer

BACKGROUND: Expression of the retinoic acid receptor β2 (RAR-β2), a putative tumor suppressor gene, is reduced in various human cancers, including squamous cell carcinomas (SCC) of the uterine cervix. The mechanism of the inhibition of RAR-β2 expression remains obscure. We examined whether methylati...

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Autores principales: Ivanova, Tatyana, Petrenko, Anatolii, Gritsko, Tatyana, Vinokourova, Svetlana, Eshilev, Ernest, Kobzeva, Vera, Kisseljov, Fjodor, Kisseljova, Natalia
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC101392/
https://www.ncbi.nlm.nih.gov/pubmed/11945179
http://dx.doi.org/10.1186/1471-2407-2-4
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author Ivanova, Tatyana
Petrenko, Anatolii
Gritsko, Tatyana
Vinokourova, Svetlana
Eshilev, Ernest
Kobzeva, Vera
Kisseljov, Fjodor
Kisseljova, Natalia
author_facet Ivanova, Tatyana
Petrenko, Anatolii
Gritsko, Tatyana
Vinokourova, Svetlana
Eshilev, Ernest
Kobzeva, Vera
Kisseljov, Fjodor
Kisseljova, Natalia
author_sort Ivanova, Tatyana
collection PubMed
description BACKGROUND: Expression of the retinoic acid receptor β2 (RAR-β2), a putative tumor suppressor gene, is reduced in various human cancers, including squamous cell carcinomas (SCC) of the uterine cervix. The mechanism of the inhibition of RAR-β2 expression remains obscure. We examined whether methylation of RAR-β2 gene could be responsible for this silencing in cervical SCC. METHODS: Expression of RAR-β2 mRNA and methylation status of the 5' region of RAR-β2 gene were examined in 20 matched specimens from patients with cervical SCC and in three cervical cancer cell lines by Northern blot analysis and methylation-specific PCR (MSP) assay or Southern blot analysis respectively. RESULTS: In 8 out 20 cervical SCC (40%) the levels of RAR-β2 mRNA were decreased or undetectable in comparison with non-neoplastic cervix tissues. All 8 tumors with reduced levels of RAR-β2 mRNA expression showed methylation of the promoter and the first exon expressed in the RAR-β2 transcript. The RAR-β2 gene from non-neoplastic cervical tissues was mostly unmethylated and expressed, but methylated alleles of the gene were found in three samples of the morphologically normal tissues adjacent to the tumors. Three cervical cancer cell lines with extremely low level of RAR-β2 mRNA expression, SiHA, HeLA and CaSki, also showed methylation of this region of the RAR-β2 gene. CONCLUSIONS: These findings suggest that methylation of the 5' region of RAR-β2 gene may contribute to gene silencing and that methylation of this region may be an important and early event in cervical carcinogenesis. These findings may be useful to make retinoids more effective as preventive and therapeutic agents in combination with inhibitors of DNA methylation.
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spelling pubmed-1013922002-04-11 Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer Ivanova, Tatyana Petrenko, Anatolii Gritsko, Tatyana Vinokourova, Svetlana Eshilev, Ernest Kobzeva, Vera Kisseljov, Fjodor Kisseljova, Natalia BMC Cancer Research Article BACKGROUND: Expression of the retinoic acid receptor β2 (RAR-β2), a putative tumor suppressor gene, is reduced in various human cancers, including squamous cell carcinomas (SCC) of the uterine cervix. The mechanism of the inhibition of RAR-β2 expression remains obscure. We examined whether methylation of RAR-β2 gene could be responsible for this silencing in cervical SCC. METHODS: Expression of RAR-β2 mRNA and methylation status of the 5' region of RAR-β2 gene were examined in 20 matched specimens from patients with cervical SCC and in three cervical cancer cell lines by Northern blot analysis and methylation-specific PCR (MSP) assay or Southern blot analysis respectively. RESULTS: In 8 out 20 cervical SCC (40%) the levels of RAR-β2 mRNA were decreased or undetectable in comparison with non-neoplastic cervix tissues. All 8 tumors with reduced levels of RAR-β2 mRNA expression showed methylation of the promoter and the first exon expressed in the RAR-β2 transcript. The RAR-β2 gene from non-neoplastic cervical tissues was mostly unmethylated and expressed, but methylated alleles of the gene were found in three samples of the morphologically normal tissues adjacent to the tumors. Three cervical cancer cell lines with extremely low level of RAR-β2 mRNA expression, SiHA, HeLA and CaSki, also showed methylation of this region of the RAR-β2 gene. CONCLUSIONS: These findings suggest that methylation of the 5' region of RAR-β2 gene may contribute to gene silencing and that methylation of this region may be an important and early event in cervical carcinogenesis. These findings may be useful to make retinoids more effective as preventive and therapeutic agents in combination with inhibitors of DNA methylation. BioMed Central 2002-03-21 /pmc/articles/PMC101392/ /pubmed/11945179 http://dx.doi.org/10.1186/1471-2407-2-4 Text en Copyright © 2002 Ivanova 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 Article
Ivanova, Tatyana
Petrenko, Anatolii
Gritsko, Tatyana
Vinokourova, Svetlana
Eshilev, Ernest
Kobzeva, Vera
Kisseljov, Fjodor
Kisseljova, Natalia
Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
title Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
title_full Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
title_fullStr Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
title_full_unstemmed Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
title_short Methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
title_sort methylation and silencing of the retinoic acid receptor-β2 gene in cervical cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC101392/
https://www.ncbi.nlm.nih.gov/pubmed/11945179
http://dx.doi.org/10.1186/1471-2407-2-4
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