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Enhanced Expression of EHMT2 Is Involved in the Proliferation of Cancer Cells through Negative Regulation of SIAH1

Authors :
Hyun-Soo Cho
John D. Kelly
Shinya Hayami
Gouji Toyokawa
Masahi Takawa
Masanori Yoshimatsu
Tatsuhiko Tsunoda
Helen I. Field
David E. Neal
Bruce A.J. Ponder
Yusuke Nakamura
Ryuji Hamamoto
Source :
Neoplasia: An International Journal for Oncology Research, Vol 13, Iss 8, Pp 676-684 (2011)
Publication Year :
2011
Publisher :
Elsevier, 2011.

Abstract

EHMT2 is a histone lysine methyltransferase localized in euchromatin regions and acting as a corepressor for specific transcription factors. Although the role of EHMT2 in transcriptional regulation has been well documented, the pathologic consequences of its dysfunction in human disease have not been well understood. Here, we describe important roles of EHMT2 in human carcinogenesis. Expression levels of EHMT2 are significantly elevated in human bladder carcinomas compared with nonneoplastic bladder tissues (P < .0001) in real-time polymerase chain reaction analysis. Complementary DNA microarray analysis also revealed its overexpression in various types of cancer. The reduction of EHMT2 expression by small interfering RNAs resulted in the suppression of the growth of cancer cells and possibly caused apoptotic cell death in cancer cells. Importantly, we show that EHMT2 can suppress transcription of the SIAH1 gene by binding to its promoter region (-293 to +51) and by methylating lysine 9 of histone H3. Furthermore, an EHMT2-specific inhibitor, BIX-01294, significantly suppressed the growth of cancer cells. Our results suggest that dysregulation of EHMT2 plays an important role in the growth regulation of cancer cells, and further functional studies may affirm the importance of EHMT2 as a promising therapeutic target for various types of cancer.

Details

Language :
English
ISSN :
14765586 and 15228002
Volume :
13
Issue :
8
Database :
Directory of Open Access Journals
Journal :
Neoplasia: An International Journal for Oncology Research
Publication Type :
Academic Journal
Accession number :
edsdoj.7fc05603e9ce4751b95757c530de19f8
Document Type :
article
Full Text :
https://doi.org/10.1593/neo.11512