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Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer
The effects of abnormalities in the DNA glycosylases NEIL1, NEIL2, and NEIL3 on human cancer have not been fully elucidated. In this paper, we found that the median somatic total mutation loads and the median somatic single nucleotide mutation loads exhibited significant inverse correlations with th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794593/ https://www.ncbi.nlm.nih.gov/pubmed/27042257 http://dx.doi.org/10.1155/2016/1546392 |
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author | Shinmura, Kazuya Kato, Hisami Kawanishi, Yuichi Igarashi, Hisaki Goto, Masanori Tao, Hong Inoue, Yusuke Nakamura, Satoki Misawa, Kiyoshi Mineta, Hiroyuki Sugimura, Haruhiko |
author_facet | Shinmura, Kazuya Kato, Hisami Kawanishi, Yuichi Igarashi, Hisaki Goto, Masanori Tao, Hong Inoue, Yusuke Nakamura, Satoki Misawa, Kiyoshi Mineta, Hiroyuki Sugimura, Haruhiko |
author_sort | Shinmura, Kazuya |
collection | PubMed |
description | The effects of abnormalities in the DNA glycosylases NEIL1, NEIL2, and NEIL3 on human cancer have not been fully elucidated. In this paper, we found that the median somatic total mutation loads and the median somatic single nucleotide mutation loads exhibited significant inverse correlations with the median NEIL1 and NEIL2 expression levels and a significant positive correlation with the median NEIL3 expression level using data for 13 cancer types from the Cancer Genome Atlas (TCGA) database. A subset of the cancer types exhibited reduced NEIL1 and NEIL2 expressions and elevated NEIL3 expression, and such abnormal expressions of NEIL1, NEIL2, and NEIL3 were also significantly associated with the mutation loads in cancer. As a mechanism underlying the reduced expression of NEIL1 in cancer, the epigenetic silencing of NEIL1 through promoter hypermethylation was found. Finally, we investigated the reason why an elevated NEIL3 expression level was associated with an increased number of somatic mutations in cancer and found that NEIL3 expression was positively correlated with the expression of APOBEC3B, a potent inducer of mutations, in diverse cancers. These results suggested that the abnormal expressions of NEIL1, NEIL2, and NEIL3 are involved in cancer through their association with the somatic mutation load. |
format | Online Article Text |
id | pubmed-4794593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47945932016-04-03 Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer Shinmura, Kazuya Kato, Hisami Kawanishi, Yuichi Igarashi, Hisaki Goto, Masanori Tao, Hong Inoue, Yusuke Nakamura, Satoki Misawa, Kiyoshi Mineta, Hiroyuki Sugimura, Haruhiko Oxid Med Cell Longev Research Article The effects of abnormalities in the DNA glycosylases NEIL1, NEIL2, and NEIL3 on human cancer have not been fully elucidated. In this paper, we found that the median somatic total mutation loads and the median somatic single nucleotide mutation loads exhibited significant inverse correlations with the median NEIL1 and NEIL2 expression levels and a significant positive correlation with the median NEIL3 expression level using data for 13 cancer types from the Cancer Genome Atlas (TCGA) database. A subset of the cancer types exhibited reduced NEIL1 and NEIL2 expressions and elevated NEIL3 expression, and such abnormal expressions of NEIL1, NEIL2, and NEIL3 were also significantly associated with the mutation loads in cancer. As a mechanism underlying the reduced expression of NEIL1 in cancer, the epigenetic silencing of NEIL1 through promoter hypermethylation was found. Finally, we investigated the reason why an elevated NEIL3 expression level was associated with an increased number of somatic mutations in cancer and found that NEIL3 expression was positively correlated with the expression of APOBEC3B, a potent inducer of mutations, in diverse cancers. These results suggested that the abnormal expressions of NEIL1, NEIL2, and NEIL3 are involved in cancer through their association with the somatic mutation load. Hindawi Publishing Corporation 2016 2016-03-03 /pmc/articles/PMC4794593/ /pubmed/27042257 http://dx.doi.org/10.1155/2016/1546392 Text en Copyright © 2016 Kazuya Shinmura et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shinmura, Kazuya Kato, Hisami Kawanishi, Yuichi Igarashi, Hisaki Goto, Masanori Tao, Hong Inoue, Yusuke Nakamura, Satoki Misawa, Kiyoshi Mineta, Hiroyuki Sugimura, Haruhiko Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer |
title | Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer |
title_full | Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer |
title_fullStr | Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer |
title_full_unstemmed | Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer |
title_short | Abnormal Expressions of DNA Glycosylase Genes NEIL1, NEIL2, and NEIL3 Are Associated with Somatic Mutation Loads in Human Cancer |
title_sort | abnormal expressions of dna glycosylase genes neil1, neil2, and neil3 are associated with somatic mutation loads in human cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794593/ https://www.ncbi.nlm.nih.gov/pubmed/27042257 http://dx.doi.org/10.1155/2016/1546392 |
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