| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Short Communications |


From the Department of Clinical Oncology,*
the Institute
of Molecular Oncology, and the Department of
Surgery,
Sir Y. K. Pao Centre for Cancer,
The Chinese University of Hong Kong, Shatin, Hong Kong, China
Using comparative genomic hybridization (CGH) analysis, we, and others, have shown that there is a high and consistent incidence of chromosome 1q copy gain in human hepatocellular carcinoma (HCC). Chromosome 1 rearrangements, that involved peri-centromeric breakpoints, have also been frequently reported in karyotypic studies of HCC. Satellite DNA hypomethylation has been postulated as the mechanism underlying the induction of chromosome 1 peri-centromeric instability in many human cancers and in individuals with the rare recessive disorder ICF (immunodeficiency, centromeric heterochromatin instability, facial anomalies). In this study, we have investigated the role of DNA hypomethylation in 1q copy gain in HCC by examining the methylation status of chromosome 1 heterochromatin DNA (band 1q12). Thirty-six histologically confirmed samples of HCC were studied (24 paired tumor and adjacent nontumorous liver tissues, and 12 tumor only). Hypomethylation of satellite 2 (Sat2) DNA in 1q12 was analyzed by Southern blotting using methyl-sensitive enzyme digestion. In parallel, all cases were analyzed by CGH. A strong correlation between hypomethylated Sat2 sequences and 1q copy gain with a 1q12 breakpoint was found (P < 0.001). We postulate that such hypomethylation alters the interaction between the CpG-rich satellite DNA and chromatin proteins, resulting in heterochromatin decondensation, breakage and aberrant 1q formation. Spectral karyotyping further supported the presence of fragile 1q12 in HCC. Of particular interest was the finding of Sat2 DNA hypomethylation in 5 of 24 adjacent nontumorous liver tissues examined. These tissues showed no evidence of malignancy on histological examination nor did they display any CGH abnormalities. Our findings suggest a role for Sat2 demethylation in the early stages of the stepwise progression of liver carcinogenesis.
This article has been cited by other articles:
![]() |
H. Gowher, H. Stuhlmann, and G. Felsenfeld Vezf1 regulates genomic DNA methylation through its effects on expression of DNA methyltransferase Dnmt3b Genes & Dev., August 1, 2008; 22(15): 2075 - 2084. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Kanai and S. Hirohashi Alterations of DNA methylation associated with abnormalities of DNA methyltransferases in human cancers during transition from a precancerous to a malignant state Carcinogenesis, December 1, 2007; 28(12): 2434 - 2442. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Davidsson, A. Andersson, K. Paulsson, M. Heidenblad, M. Isaksson, A. Borg, J. Heldrup, M. Behrendtz, I. Panagopoulos, T. Fioretos, et al. Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3 Hum. Mol. Genet., September 15, 2007; 16(18): 2215 - 2225. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Suetake, D. Hayata, and S. Tajima The Amino-Terminus of Mouse DNA Methyltransferase 1 Forms an Independent Domain and Binds to DNA with the Sequence Involving PCNA Binding Motif J. Biochem., December 1, 2006; 140(6): 763 - 776. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. B. Jenkins, H. Blair, K. V. Ballman, C. Giannini, R. M. Arusell, M. Law, H. Flynn, S. Passe, S. Felten, P. D. Brown, et al. A t(1;19)(q10;p10) Mediates the Combined Deletions of 1p and 19q and Predicts a Better Prognosis of Patients with Oligodendroglioma. Cancer Res., October 15, 2006; 66(20): 9852 - 9861. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Cadieux, T.-T. Ching, S. R. VandenBerg, and J. F. Costello Genome-wide Hypomethylation in Human Glioblastomas Associated with Specific Copy Number Alteration, Methylenetetrahydrofolate Reductase Allele Status, and Increased Proliferation. Cancer Res., September 1, 2006; 66(17): 8469 - 8476. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. V. Karpinets and B. D. Foy Tumorigenesis: the adaptation of mammalian cells to sustained stress environment by epigenetic alterations and succeeding matched mutations Carcinogenesis, August 1, 2005; 26(8): 1323 - 1334. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Widschwendter, G. Jiang, C. Woods, H. M. Muller, H. Fiegl, G. Goebel, C. Marth, E. Muller-Holzner, A. G. Zeimet, P. W. Laird, et al. DNA Hypomethylation and Ovarian Cancer Biology Cancer Res., July 1, 2004; 64(13): 4472 - 4480. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Bilger, L. M. Bennett, R. A. Carabeo, T. A. Chiaverotti, C. Dvorak, K. M. Liss, S. A. Schadewald, H. C. Pitot, and N. R. Drinkwater A Potent Modifier of Liver Cancer Risk on Distal Mouse Chromosome 1: Linkage Analysis and Characterization of Congenic Lines Genetics, June 1, 2004; 167(2): 859 - 866. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Eden, F. Gaudet, A. Waghmare, and R. Jaenisch Chromosomal Instability and Tumors Promoted by DNA Hypomethylation Science, April 18, 2003; 300(5618): 455 - 455. [Full Text] [PDF] |
||||
![]() |
H. Tsuda, T. Takarabe, Y. Kanai, T. Fukutomi, and S. Hirohashi Correlation of DNA Hypomethylation at Pericentromeric Heterochromatin Regions of Chromosomes 16 and 1 with Histological Features and Chromosomal Abnormalities of Human Breast Carcinomas Am. J. Pathol., September 1, 2002; 161(3): 859 - 866. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Saito, Y. Kanai, M. Sakamoto, H. Saito, H. Ishii, and S. Hirohashi Overexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis PNAS, July 23, 2002; 99(15): 10060 - 10065. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |