Cargando…
LINE-1 methylation patterns of different loci in normal and cancerous cells
This study evaluated methylation patterns of long interspersed nuclear element-1 (LINE-1) sequences from 17 loci in several cell types, including squamous cell cancer cell lines, normal oral epithelium (NOE), white blood cells and head and neck squamous cell cancers (HNSCC). Although sequences of ea...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2553567/ https://www.ncbi.nlm.nih.gov/pubmed/18776216 http://dx.doi.org/10.1093/nar/gkn571 |
_version_ | 1782159511991091200 |
---|---|
author | Phokaew, Chureerat Kowudtitham, Supakit Subbalekha, Keskanya Shuangshoti, Shanop Mutirangura, Apiwat |
author_facet | Phokaew, Chureerat Kowudtitham, Supakit Subbalekha, Keskanya Shuangshoti, Shanop Mutirangura, Apiwat |
author_sort | Phokaew, Chureerat |
collection | PubMed |
description | This study evaluated methylation patterns of long interspersed nuclear element-1 (LINE-1) sequences from 17 loci in several cell types, including squamous cell cancer cell lines, normal oral epithelium (NOE), white blood cells and head and neck squamous cell cancers (HNSCC). Although sequences of each LINE-1 are homologous, LINE-1 methylation levels at each locus are different. Moreover, some loci demonstrate the different methylation levels between normal tissue types. Interestingly, in some chromosomal regions, wider ranges of LINE-1 methylation levels were observed. In cancerous cells, the methylation levels of most LINE-1 loci demonstrated a positive correlation with each other and with the genome-wide levels. Therefore, the loss of genome-wide methylation in cancerous cells occurs as a generalized process. However, different LINE-1 loci showed different incidences of HNSCC hypomethylation, which is a lower methylation level than NOE. Additionally, we report a closer direct association between two LINE-1s in different EPHA3 introns. Finally, hypermethylation of some LINE-1s can be found sporadically in cancer. In conclusion, even though the global hypomethylation process that occurs in cancerous cells can generally deplete LINE-1 methylation levels, LINE-1 methylation can be influenced differentially depending on where the particular sequences are located in the genome. |
format | Text |
id | pubmed-2553567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25535672008-10-01 LINE-1 methylation patterns of different loci in normal and cancerous cells Phokaew, Chureerat Kowudtitham, Supakit Subbalekha, Keskanya Shuangshoti, Shanop Mutirangura, Apiwat Nucleic Acids Res Molecular Biology This study evaluated methylation patterns of long interspersed nuclear element-1 (LINE-1) sequences from 17 loci in several cell types, including squamous cell cancer cell lines, normal oral epithelium (NOE), white blood cells and head and neck squamous cell cancers (HNSCC). Although sequences of each LINE-1 are homologous, LINE-1 methylation levels at each locus are different. Moreover, some loci demonstrate the different methylation levels between normal tissue types. Interestingly, in some chromosomal regions, wider ranges of LINE-1 methylation levels were observed. In cancerous cells, the methylation levels of most LINE-1 loci demonstrated a positive correlation with each other and with the genome-wide levels. Therefore, the loss of genome-wide methylation in cancerous cells occurs as a generalized process. However, different LINE-1 loci showed different incidences of HNSCC hypomethylation, which is a lower methylation level than NOE. Additionally, we report a closer direct association between two LINE-1s in different EPHA3 introns. Finally, hypermethylation of some LINE-1s can be found sporadically in cancer. In conclusion, even though the global hypomethylation process that occurs in cancerous cells can generally deplete LINE-1 methylation levels, LINE-1 methylation can be influenced differentially depending on where the particular sequences are located in the genome. Oxford University Press 2008-10 2008-09-06 /pmc/articles/PMC2553567/ /pubmed/18776216 http://dx.doi.org/10.1093/nar/gkn571 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Molecular Biology Phokaew, Chureerat Kowudtitham, Supakit Subbalekha, Keskanya Shuangshoti, Shanop Mutirangura, Apiwat LINE-1 methylation patterns of different loci in normal and cancerous cells |
title | LINE-1 methylation patterns of different loci in normal and cancerous cells |
title_full | LINE-1 methylation patterns of different loci in normal and cancerous cells |
title_fullStr | LINE-1 methylation patterns of different loci in normal and cancerous cells |
title_full_unstemmed | LINE-1 methylation patterns of different loci in normal and cancerous cells |
title_short | LINE-1 methylation patterns of different loci in normal and cancerous cells |
title_sort | line-1 methylation patterns of different loci in normal and cancerous cells |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2553567/ https://www.ncbi.nlm.nih.gov/pubmed/18776216 http://dx.doi.org/10.1093/nar/gkn571 |
work_keys_str_mv | AT phokaewchureerat line1methylationpatternsofdifferentlociinnormalandcancerouscells AT kowudtithamsupakit line1methylationpatternsofdifferentlociinnormalandcancerouscells AT subbalekhakeskanya line1methylationpatternsofdifferentlociinnormalandcancerouscells AT shuangshotishanop line1methylationpatternsofdifferentlociinnormalandcancerouscells AT mutiranguraapiwat line1methylationpatternsofdifferentlociinnormalandcancerouscells |