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Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients

Recent studies suggest that aberrant DNA methylation might occur early and commonly in colorectal tumorigenesis. In 111 normal subjects, the mean LINE-1 methylation level of peripheral blood was 81.0 ± 5.7%. Of 143 colorectal cancer (CRC) patients, the mean level of LINE-1 methylation was 60.5 ± 12....

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Autores principales: Kuan, Tai-Chuan, Lin, Pei-Ching, Yang, Shung-Haur, Lin, Chun-Chi, Lan, Yuan-Tzu, Lin, Hung-Hsin, Liang, Wen-Yi, Chen, Wei-Shone, Lin, Jen-Kou, Jiang, Jeng-Kai, Chang, Shih-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993106/
https://www.ncbi.nlm.nih.gov/pubmed/29795620
http://dx.doi.org/10.1371/journal.pone.0197681
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author Kuan, Tai-Chuan
Lin, Pei-Ching
Yang, Shung-Haur
Lin, Chun-Chi
Lan, Yuan-Tzu
Lin, Hung-Hsin
Liang, Wen-Yi
Chen, Wei-Shone
Lin, Jen-Kou
Jiang, Jeng-Kai
Chang, Shih-Ching
author_facet Kuan, Tai-Chuan
Lin, Pei-Ching
Yang, Shung-Haur
Lin, Chun-Chi
Lan, Yuan-Tzu
Lin, Hung-Hsin
Liang, Wen-Yi
Chen, Wei-Shone
Lin, Jen-Kou
Jiang, Jeng-Kai
Chang, Shih-Ching
author_sort Kuan, Tai-Chuan
collection PubMed
description Recent studies suggest that aberrant DNA methylation might occur early and commonly in colorectal tumorigenesis. In 111 normal subjects, the mean LINE-1 methylation level of peripheral blood was 81.0 ± 5.7%. Of 143 colorectal cancer (CRC) patients, the mean level of LINE-1 methylation was 60.5 ± 12.5%. We defined below 60% as cut-off value of LINE-1 hypomethylation, and 93 cases (65.0%) had LINE-1 hypomethylation in the tumor tissue. LINE-1 hypomethylation was not associated with any other clinical features. There was a trend that LINE-1 hypomethylation tumors were associated with advanced disease, but it did not reach statistical significance. There was no significant association between mutations of 12 genes, MSI-high, EMAST, and LINE-1 hypomethylation level. The median follow-up was 61.2 months. Five-year disease-free survival (DFS) and overall survival curves of patients with LINE-1 hypomethylation tumors were significantly lower than those of patients with normal LINE-1 methylation tumors (p = 0.032 and 0.001, respectively). Multivariate analysis showed that only TNM staging was an independent prognostic factor for CRC patients including DFS and overall survival (OS). LINE-1 did not impact patients’ outcomes in multivariate analysis including DFS and OS. In conclusion, LINE-1 hypomethylation is marginally related to advanced stage CRC and impacts patients’ outcomes in univariate analysis.
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spelling pubmed-59931062018-06-17 Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients Kuan, Tai-Chuan Lin, Pei-Ching Yang, Shung-Haur Lin, Chun-Chi Lan, Yuan-Tzu Lin, Hung-Hsin Liang, Wen-Yi Chen, Wei-Shone Lin, Jen-Kou Jiang, Jeng-Kai Chang, Shih-Ching PLoS One Research Article Recent studies suggest that aberrant DNA methylation might occur early and commonly in colorectal tumorigenesis. In 111 normal subjects, the mean LINE-1 methylation level of peripheral blood was 81.0 ± 5.7%. Of 143 colorectal cancer (CRC) patients, the mean level of LINE-1 methylation was 60.5 ± 12.5%. We defined below 60% as cut-off value of LINE-1 hypomethylation, and 93 cases (65.0%) had LINE-1 hypomethylation in the tumor tissue. LINE-1 hypomethylation was not associated with any other clinical features. There was a trend that LINE-1 hypomethylation tumors were associated with advanced disease, but it did not reach statistical significance. There was no significant association between mutations of 12 genes, MSI-high, EMAST, and LINE-1 hypomethylation level. The median follow-up was 61.2 months. Five-year disease-free survival (DFS) and overall survival curves of patients with LINE-1 hypomethylation tumors were significantly lower than those of patients with normal LINE-1 methylation tumors (p = 0.032 and 0.001, respectively). Multivariate analysis showed that only TNM staging was an independent prognostic factor for CRC patients including DFS and overall survival (OS). LINE-1 did not impact patients’ outcomes in multivariate analysis including DFS and OS. In conclusion, LINE-1 hypomethylation is marginally related to advanced stage CRC and impacts patients’ outcomes in univariate analysis. Public Library of Science 2018-05-24 /pmc/articles/PMC5993106/ /pubmed/29795620 http://dx.doi.org/10.1371/journal.pone.0197681 Text en © 2018 Kuan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kuan, Tai-Chuan
Lin, Pei-Ching
Yang, Shung-Haur
Lin, Chun-Chi
Lan, Yuan-Tzu
Lin, Hung-Hsin
Liang, Wen-Yi
Chen, Wei-Shone
Lin, Jen-Kou
Jiang, Jeng-Kai
Chang, Shih-Ching
Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
title Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
title_full Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
title_fullStr Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
title_full_unstemmed Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
title_short Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
title_sort impact of line-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993106/
https://www.ncbi.nlm.nih.gov/pubmed/29795620
http://dx.doi.org/10.1371/journal.pone.0197681
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