Literature DB >> 16093442

The antiproliferative agent MLN944 preferentially inhibits transcription.

Sarah A Byers1, Blanca Schafer, Darshan S Sappal, Jeffery Brown, David H Price.   

Abstract

MLN944 is a novel compound currently being codeveloped by Millennium Pharmaceuticals and Xenova Ltd. as a cancer therapeutic and is in a phase I clinical trial for solid tumors. Although MLN944 was originally proposed to function as a topoisomerase I and II inhibitor, more recent data has shown that it is a DNA-intercalating agent that does not inhibit the catalytic activity of topoisomerase I or II. We show here that MLN944 inhibits incorporation of radiolabeled precursors into RNA preferentially over incorporation into DNA and protein in HCT116 and H460 cells. To determine if MLN944 inhibits transcription, a human RNA polymerase II in vitro transcription system was used. MLN944 inhibited initiation when added before or after the formation of preinitiation complexes and inhibited elongation at higher concentrations. The preferential inhibition of initiation differentiates MLN944 from actinomycin D, which more strongly inhibits elongation. Transcription of all RNA polymerases was inhibited in nuclei isolated from HeLa cells treated with low concentrations of MLN944. Our data are consistent with transcription as the target of the potent cytotoxic effects of MLN944.

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Year:  2005        PMID: 16093442     DOI: 10.1158/1535-7163.MCT-05-0109

Source DB:  PubMed          Journal:  Mol Cancer Ther        ISSN: 1535-7163            Impact factor:   6.261


  7 in total

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2.  PLIP 2021: expanding the scope of the protein-ligand interaction profiler to DNA and RNA.

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Authors:  Sebastian Biglione; Sarah A Byers; Jason P Price; Van Trung Nguyen; Olivier Bensaude; David H Price; Wendy Maury
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5.  First-into-man phase I and pharmacokinetic study of XR5944.14, a novel agent with a unique mechanism of action.

Authors:  W Verborg; H Thomas; D Bissett; J Waterfall; J Steiner; M Cooper; E M Rankin
Journal:  Br J Cancer       Date:  2007-09-11       Impact factor: 7.640

Review 6.  Selective antagonism of cJun for cancer therapy.

Authors:  Andrew Brennan; James T Leech; Neil M Kad; Jody M Mason
Journal:  J Exp Clin Cancer Res       Date:  2020-09-11

Review 7.  Novel DNA Bis-Intercalator XR5944 as a Potent Anticancer Drug-Design and Mechanism of Action.

Authors:  Adam J Buric; Jonathan Dickerhoff; Danzhou Yang
Journal:  Molecules       Date:  2021-07-07       Impact factor: 4.411

  7 in total

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