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Blood, 1 August 2006, Vol. 108, No. 3, pp. 1058-1064.
Prepublished online as a Blood First Edition Paper on April 18, 2006; DOI 10.1182/blood-2005-08-007377.


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NEOPLASIA

STAT3 induces transcription of the DNA methyltransferase 1 gene (DNMT1) in malignant T lymphocytes

Qian Zhang, Hong Y. Wang, Anders Woetmann, Puthiyaveettil N. Raghunath, Niels Odum, and Mariusz A. Wasik

From the Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA; and the Department of Molecular Biology, University of Copenhagen, Copenhagen, Denmark.

In this study, we demonstrated that STAT3, a well-characterized transcription factor expressed in continuously activated oncogenic form in the large spectrum of cancer types, induces in malignant T lymphocytes the expression of DNMT1, the key effector of epigenetic gene silencing. STAT3 binds in vitro to 2 STAT3 SIE/GAS-binding sites identified in promoter 1 and enhancer 1 of the DNMT1 gene. STAT3 also binds to the promoter 1 region and induces its activity in vivo. Treatment of the malignant T lymphocytes with STAT3 siRNA abrogates expression of DNMT1, inhibits cell growth, and induces programmed cell death. In turn, inhibition of DNMT1 by a small molecule inhibitor, 5-aza-2-deoxy-cytidine, and 2 DNMT1 antisense DNA oligonucleotides inhibits the phosphorylation of STAT3. These data indicate that STAT3 may in part transform cells by fostering epigenetic silencing of tumor-suppressor genes. They also indicate that by inducing DNMT1, STAT3 facilitates its own persistent activation in malignant T cells. Finally, these data provide further rationale for therapeutically targeting STAT3 in T-cell lymphomas and, possibly, other malignancies.


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