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

Author

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  • Tai-Chuan Kuan
  • Pei-Ching Lin
  • Shung-Haur Yang
  • Chun-Chi Lin
  • Yuan-Tzu Lan
  • Hung-Hsin Lin
  • Wen-Yi Liang
  • Wei-Shone Chen
  • Jen-Kou Lin
  • Jeng-Kai Jiang
  • Shih-Ching Chang

Abstract

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.

Suggested Citation

  • Tai-Chuan Kuan & Pei-Ching Lin & Shung-Haur Yang & Chun-Chi Lin & Yuan-Tzu Lan & Hung-Hsin Lin & Wen-Yi Liang & Wei-Shone Chen & Jen-Kou Lin & Jeng-Kai Jiang & Shih-Ching Chang, 2018. "Impact of LINE-1 hypomethylation on the clinicopathological and molecular features of colorectal cancer patients," PLOS ONE, Public Library of Science, vol. 13(5), pages 1-12, May.
  • Handle: RePEc:plo:pone00:0197681
    DOI: 10.1371/journal.pone.0197681
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