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

被引:58
作者
Kitkumthorn, Nakarin [3 ]
Tuangsintanakul, Time [1 ,2 ]
Rattanatanyong, Prakasit [2 ]
Tiwawech, Danai [1 ]
Mutirangura, Apiwat [2 ]
机构
[1] Natl Canc Inst, Div Res, Bangkok 10400, Thailand
[2] Chulalongkorn Univ, Fac Med, Dept Anat, Ctr Excellence Mol Genet Canc & Human Dis, Bangkok 10330, Thailand
[3] Mahidol Univ, Fac Dent, Dept Oral & Maxillofacial Surg, Bangkok 10400, Thailand
关键词
LINE-1; methylation; COBRA LINE-1; Level and pattern; Peripheral blood mononuclear cells; Cancer; GLOBAL DNA METHYLATION; PROMOTER HYPERMETHYLATION; BLADDER-CANCER; NUCLEIC-ACIDS; HYPOMETHYLATION; BIOMARKER; LEVEL; RISK; SUSCEPTIBILITY; CARCINOMA;
D O I
10.1016/j.cca.2012.01.024
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:869 / 874
页数:6
相关论文
共 35 条
[1]   Hypomethylation of Intragenic LINE-1 Represses Transcription in Cancer Cells through AGO2 [J].
Aporntewan, Chatchawit ;
Phokaew, Chureerat ;
Piriyapongsa, Jittima ;
Ngamphiw, Chumpol ;
Ittiwut, Chupong ;
Tongsima, Sissades ;
Mutirangura, Apiwat .
PLOS ONE, 2011, 6 (03)
[2]   Differential repetitive DNA methylation in multiple myeloma molecular subgroups [J].
Bollati, Valentina ;
Fabris, Sonia ;
Pegoraro, Valeria ;
Ronchetti, Domenica ;
Mosca, Laura ;
Deliliers, Giorgio Lambertenghi ;
Motta, Valeria ;
Bertazzi, Pier Alberto ;
Baccarelli, Andrea ;
Neri, Antonino .
CARCINOGENESIS, 2009, 30 (08) :1330-1335
[3]   Distinctive pattern of LINE-1 methylation level in normal tissues and the association with carcinogenesis [J].
Chalitchagorn, K ;
Shuangshoti, S ;
Hourpai, N ;
Kongruttanachok, N ;
Tangkijvanich, P ;
Thong-ngam, D ;
Voravud, N ;
Sriuranpong, V ;
Mutirangura, A .
ONCOGENE, 2004, 23 (54) :8841-8846
[4]   Hypomethylation of LINE-1 and Alu in well-differentiated neuroendocrine tumors (pancreatic endocrine tumors and carcinoid tumors) [J].
Choi, In-Seon ;
Estecio, Marcos R. H. ;
Nagano, Yasuhiko ;
Kim, Do Ha ;
White, Jill A. ;
Yao, James C. ;
Issa, Jean-Pierre J. ;
Rashid, Asif .
MODERN PATHOLOGY, 2007, 20 (07) :802-810
[5]   Changes in DNA methylation of tandem DNA repeats are different from interspersed repeats in cancer [J].
Choi, Si Ho ;
Worswick, Scott ;
Byun, Hyang-Min ;
Shear, Talia ;
Soussa, John C. ;
Wolff, Erika M. ;
Douer, Dan ;
Garcia-Manero, Guillermo ;
Liang, Gangning ;
Yang, Allen S. .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (03) :723-729
[6]   Global DNA Hypomethyation (LINE-1) in the Normal Colon and Lifestyle Characteristics and Dietary and Genetic Factors [J].
Figueiredo, Jane C. ;
Grau, Maria V. ;
Wallace, Kristin ;
Levine, A. Joan ;
Shen, Lanlan ;
Hamdan, Randala ;
Chen, Xinli ;
Bresalier, Robert S. ;
McKeown-Eyssen, Gail ;
Haile, Robert W. ;
Baron, John A. ;
Issa, Jean-Pierre J. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2009, 18 (04) :1041-1049
[7]   Global DNA methylation is influenced by smoking behaviour [J].
Hillemacher, Thomas ;
Frieling, Helge ;
Moskau, Susanna ;
Muschler, Marc A. N. ;
Semmler, Alexander ;
Kornhuber, Johannes ;
Klockgether, Thomas ;
Bleich, Stefan ;
Linnebank, Michael .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2008, 18 (04) :295-298
[8]   Causes and consequences of DNA hypomethylation in human cancer [J].
Hoffmann, MJ ;
Schulz, WA .
BIOCHEMISTRY AND CELL BIOLOGY, 2005, 83 (03) :296-321
[9]   Blood leukocyte DNA hypomethylation and gastric cancer risk in a high-risk Polish population [J].
Hou, Lifang ;
Wang, Hao ;
Sartori, Samantha ;
Gawron, Andrew ;
Lissowska, Jolanta ;
Bollati, Valentina ;
Tarantini, Letizia ;
Zhang, Fang Fang ;
Zatonski, Witold ;
Chow, Wong-Ho ;
Baccarelli, Andrea .
INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (08) :1866-1874
[10]   Global DNA methylation level in whole blood as a biomarker in head and neck squamous cell carcinoma [J].
Hsiung, Debra Ting ;
Marsit, Carmen J. ;
Houseman, E. Andres ;
Eddy, Karen ;
Furniss, C. Sloane ;
McClean, Michael D. ;
Kelsey, Karl T. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2007, 16 (01) :108-114