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* Molecular Pharmacology and Therapeutics Program, Memorial
Sloan-Kettering Cancer Center and the Weill Graduate School of Medical
Sciences of Cornell University, 1275 York Avenue, New York, NY 10021;
and Edited by Samuel J. Danishefsky, Memorial Sloan-Kettering Cancer
Center, New York, NY, and approved April 3, 2000 (received for review November 29, 1999)
Ecteinascidin 743 (ET-743), a highly promising marine-based
antitumor agent presently in phase II clinical trials, has been shown
to interfere with the binding of minor-groove-interacting transcription
factors, particularly NF-Y, with their cognate promoter elements
in vitro. We have shown that NF-Y is a central mediator of activation of transcription of the human P glycoprotein gene (MDR1)
by a variety of inducers and that NF-Y functions by recruiting the
histone acetyltransferase PCAF to the MDR1 promoter. In the present
study, we tested whether ET-743 could block activation of the MDR1
promoter by agents that mediate their effect through the NF-Y/PCAF
complex. We report that physiologically relevant concentrations of
ET-743 abrogate transcriptional activation of both the
endogenous MDR1 gene and MDR1 reporter constructs by the
histone deacetylase inhibitors as well as by UV light, with minimal
effect on constitutive MDR1 transcription. Notably, this inhibition
does not alter the promoter-associated histone hyperacetylation induced
by histone deacetylase inhibitors, suggesting an in vivo molecular target downstream of NF-Y/PCAF binding. ET-743 is therefore the prototype for a distinct class of transcription-targeted
chemotherapeutic agents and may be an efficacious adjuvant to the
treatment of multidrug-resistant tumors.
Medical Sciences
Ecteinascidin 743, a transcription-targeted chemotherapeutic that
inhibits MDR1 activation
, and
PharmaMar USA, 320 Putnam Avenue, Cambridge, MA 02139
To whom reprint requests should be addressed.
E-mail: k-scotto{at}ski.mskcc.org.
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