Maehata T, Taniguchi H, Yamamoto H, Nosho K, Adachi Y, Miyamoto N, Miyamoto C, Akutsu N, Yamaoka S, Itoh F. Transcriptional silencing of Dickkopf gene family by CpG island hypermethylation in human gastrointestinal cancer. World J Gastroenterol 2008; 14(17): 2702-2714 [PMID: 18461655 DOI: 10.3748/wjg.14.2702]
Corresponding Author of This Article
Hiroyuki Yamamoto, MD, FJSIM, PhD, First Department of Internal Medicine, Sapporo Medical University, S.-1, W.-16, Chuo-ku, Sapporo 060-8543, Japan. h-yama@sapmed.ac.jp
Article-Type of This Article
Gastric Cancer
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Tadateru Maehata, Fumio Itoh, Department of Gastroenterology and Hepatology, St. Marianna University School of Medicine, Kanagawa 216-8511, Japan
Hiroaki Taniguchi, Hiroyuki Yamamoto, Katsuhiko Nosho, Yasushi Adachi, Nobuki Miyamoto, Chie Miyamoto, Noriyuki Akutsu, Satoshi Yamaoka, First Department of Internal Medicine, Sapporo Medical University, Sapporo 060-8543, Japan
Author contributions: Maehata T, Taniguchi H, Yamamoto H designed research; Maehata T, Taniguchi H, Yamamoto H, Nosho K, Adachi Y, Akutsu N, and Yamaoka S performed research; Maehata T, Taniguchi H, Yamamoto H, Miyamoto N, and Miyamoto C analyzed data; and Maehata T, Taniguchi H, Yamamoto H, and Itoh F wrote the paper.
Correspondence to: Hiroyuki Yamamoto, MD, FJSIM, PhD, First Department of Internal Medicine, Sapporo Medical University, S.-1, W.-16, Chuo-ku, Sapporo 060-8543, Japan. h-yama@sapmed.ac.jp
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Received: October 27, 2007 Revised: February 15, 2008 Published online: May 7, 2008
Abstract
AIM: To clarify alterations of Dickkopfs (Dkks) and Kremen2 (Krm2) in gastrointestinal cancer.
METHODS: We investigated the expression profiles and epigenetic alterations of Dkks and Krm2 genes in gastrointestinal cancer using RT-PCR, tissue microarray analysis, and methylation specific PCR (MSP). Cancer cells were treated with the demethylating agent and/or histone deacetylase inhibitor. WST-8 assays and in vitro invasion assays after treatment with specific siRNA for those genes were performed.
RESULTS: Dkks and Krm2 expression levels were reduced in a certain subset of the gastrointestinal cancer cell lines and cancer tissues. This was correlated with promoter hypermethylation. There were significant correlations between Dkks over-expression levels and beta-catenin over-expression in colorectal cancer. In colorectal cancers with beta-catenin over-expression, Dkk-1 expression levels were significantly lower in those with lymph node metastases than in those without. Down-regulation of Dkks expression by siRNA resulted in a significant increase in cancer cell growth and invasiveness in vitro.
CONCLUSION: Down-regulation of the Dkks associated to promoter hypermethylation appears to be frequently involved in gastrointestinal tumorigenesis.
