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Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q

Loss of heterozygosity at several chromosomal loci is frequently observed in human cancers and loss of one allele is supposed to affect expression of the gene(s) in the remaining allele. As DNA methylation is known to be closely related to gene expression in vertebrates, we are interested in the met...

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Detalles Bibliográficos
Autores principales: Shiraishi, Masahiko, Sekiya, Takao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917876/
https://www.ncbi.nlm.nih.gov/pubmed/2482283
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01627.x
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author Shiraishi, Masahiko
Sekiya, Takao
author_facet Shiraishi, Masahiko
Sekiya, Takao
author_sort Shiraishi, Masahiko
collection PubMed
description Loss of heterozygosity at several chromosomal loci is frequently observed in human cancers and loss of one allele is supposed to affect expression of the gene(s) in the remaining allele. As DNA methylation is known to be closely related to gene expression in vertebrates, we are interested in the methylation status of the regions of alleles remaining after loss of their counterparts. In this work we investigated the methylation status of DNA from human lung carcinoma in which heterozygosity was lost at 3p and 13q and found that the remaining allele at these loci was preferentially demethylated. In contrast, tumor DNAs without allele loss tended to retain highly methylated states. These results suggest that in tumors, change of the DNA methylation status is closely related with allele loss, and vice versa.
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spelling pubmed-59178762018-05-11 Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q Shiraishi, Masahiko Sekiya, Takao Jpn J Cancer Res Rapid Communication Loss of heterozygosity at several chromosomal loci is frequently observed in human cancers and loss of one allele is supposed to affect expression of the gene(s) in the remaining allele. As DNA methylation is known to be closely related to gene expression in vertebrates, we are interested in the methylation status of the regions of alleles remaining after loss of their counterparts. In this work we investigated the methylation status of DNA from human lung carcinoma in which heterozygosity was lost at 3p and 13q and found that the remaining allele at these loci was preferentially demethylated. In contrast, tumor DNAs without allele loss tended to retain highly methylated states. These results suggest that in tumors, change of the DNA methylation status is closely related with allele loss, and vice versa. Blackwell Publishing Ltd 1989-10 /pmc/articles/PMC5917876/ /pubmed/2482283 http://dx.doi.org/10.1111/j.1349-7006.1989.tb01627.x Text en
spellingShingle Rapid Communication
Shiraishi, Masahiko
Sekiya, Takao
Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q
title Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q
title_full Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q
title_fullStr Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q
title_full_unstemmed Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q
title_short Change in Methylation Status of DNA of Remaining Allele in Human Lung Cancers with Loss of Heterozygosity on Chromosomes 3p and 13q
title_sort change in methylation status of dna of remaining allele in human lung cancers with loss of heterozygosity on chromosomes 3p and 13q
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917876/
https://www.ncbi.nlm.nih.gov/pubmed/2482283
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01627.x
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