4.7 Article

LINE-1 methylation in the peripheral blood mononuclear cells of cancer patients

Journal

CLINICA CHIMICA ACTA
Volume 413, Issue 9-10, Pages 869-874

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cca.2012.01.024

Keywords

LINE-1 methylation; COBRA LINE-1; Level and pattern; Peripheral blood mononuclear cells; Cancer

Funding

  1. National Science and Technology Development Agency (NSTDA), Thailand
  2. Four Seasons Hotel Bangkok's 4th Cancer Care charity
  3. Thai Red Cross Society, Chulalongkorn University
  4. TRF-MRG [MRG5380010]

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Background: Recently, we classified LINE-1 loci according to their methylation statuses and found that the percentage of hypomethylated LINE-1 loci ((CC)-C-u-C-u) can differentiate between the peripheral blood mononuclear cells (PBMCs) of oral cancer patients and normal controls with a higher specificity and sensitivity than overall methylation levels. Here, we evaluated the LINE-1 methylation levels and patterns in PBMCs from patients with cancers of the nasopharynx, lung, liver, bile duct, breast and colon. Methods: Combined Bisulfite Restriction Analysis (COBRA) of LINE-1 loci was performed to examine the LINE-1 methylation statuses of PBMCs from 216 cancer patients with 6 different types of cancer compared with 144 normal controls. Results: Only colorectal and nasopharyngeal cancer samples were found to have lower levels of overall LINE-1 methylation compared with normal controls (p<0.0001 and p = 0.0022). However, %(CC)-C-u-C-u in cancers of the colon, liver, lung and nasopharynx was significantly higher compared with normal controls (p<0.0001, p<0.0001, p = 0.01 and p=0.001. respectively). Furthermore, ROC curve analyses of these four cancer types also demonstrated the potential of %(CC)-C-u-C-u as a biomarker for cancer diagnosis. Conclusion: Changes in the levels and patterns of genome-wide methylation of PBMCs are associated with cancer risk. For LINE-1, %(CC)-C-u-C-u is a more effective tumour marker for determining cancer risk than overall methylation levels. (C) 2012 Elsevier B.V. All rights reserved.

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