Journal article

Targeting RNA polymerase I with an oral small molecule CX-5461 inhibits ribosomal RNA synthesis and solid tumor growth

D Drygin, A Lin, J Bliesath, CB Ho, SE O'Brien, C Proffitt, M Omori, M Haddach, MK Schwaebe, A Siddiqui-Jain, N Streiner, JE Quin, E Sanij, MJ Bywater, RD Hannan, D Ryckman, K Anderes, WG Rice

Cancer Research | Published : 2011

Abstract

Deregulated ribosomal RNA synthesis is associated with uncontrolled cancer cell proliferation. RNA polymerase (Pol) I, the multiprotein complex that synthesizes rRNA, is activated widely in cancer. Thus, selective inhibitors of Pol I may offer a general therapeutic strategy to block cancer cell proliferation. Coupling medicinal chemistry efforts to tandem cell- and molecular-based screening led to the design of CX-5461, a potent small-molecule inhibitor of rRNA synthesis in cancer cells. CX-5461 selectively inhibits Pol I - driven transcription relative to Pol II-driven transcription, DNA replication, and protein translation. Molecular studies demonstrate that CX-5461 inhibits the initiation..

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University of Melbourne Researchers

Grants

Funding Acknowledgements

This work was supported in part by Cylene Pharmaceuticals Inc. and in part by grants to R.D. Hannan and E. Sanij from the National Health and Medical Research Council (NHMRC) of Australia. R.D. Hannan was supported by a research fellowship from the NHMRC. M.J. Bywater was supported by an NHMRC postgraduate scholarship. J.E. Quin was supported by an Australian postgraduate award.