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  A Small-Molecule Inhibitor of BCL6 Kills DLBCL Cells In Vitro and In Vivo

Cerchietti, L. C., Ghetu, A., Zhu, X., Da Silva, G., Zhong, S., Matthews, M., et al. (2010). A Small-Molecule Inhibitor of BCL6 Kills DLBCL Cells In Vitro and In Vivo. Cancer Cell, 17(4), 400-411. doi:10.1016/j.ccr.2009.12.050.

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 Creators:
Cerchietti , L. C.1, 2, Author
Ghetu , A.F.3, Author
Zhu, X.4, Author
Da Silva , G.F.5, Author
Zhong, S.4, Author
Matthews , M.4, Author
Bunting , K.L.1, 2, Author
Polo, J.M.5, Author
Farès, C.3, 6, Author           
Arrowsmith, C.H.3, 7, Author
Ning Yang, S.1, 2, Author
Garcia, M.1, 2, Author
Coop, A.4, Author
MacKerell Jr. , A.D.4, Author
Privé , G.G.3, 7, 8, Author
Melnick, A.1, 2, Author
Affiliations:
1Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medical College, Cornell University, New York, NY 10065, USA, ou_persistent22              
2Department of Pharmacology, Weill Cornell Medical College, Cornell University, New York, NY 10065, USA, ou_persistent22              
3Ontario Cancer Institute and Campbell Family Institute for Cancer Research, Toronto, ON M5G 1L7, Canada, ou_persistent22              
4Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD 21201, USA, ou_persistent22              
5Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA, ou_persistent22              
6Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_persistent22              
7Department of Medical Biophysics, University of Toronto, Toronto, ON M5G 2N9, Canada, ou_persistent22              
8Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada, ou_persistent22              

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Free keywords: CELLCYCLE; CHEMBIO
 Abstract: BCL6 is the most commonly involved oncogene in B cell lymphomas. Depletion or blockade of BCL6 potently kills DLBCL cells and BCL6 is thus a critical therapeutic target. Like many oncogenes and tumors suppressors, BCL6 is a transcription factor. Because such proteins usually mediate their actions through extensive protein interaction surfaces, they have been considered nonamenable to targeting with small molecules. Herein, we used an integrated biochemical and computational approach to identify an effective and specific BCL6 small-molecule inhibitor. This drug displayed favorable pharmacokinetics, pharmacodynamics, toxicity, and therapeutic efficacy. This work demonstrates that oncogenic transcriptional repressors can be therapeutically targeted with small molecules and presents a rationally designed transcription therapy approach for the treatment of lymphomas.

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Language(s): eng - English
 Dates: 2010-04-122010-04-13
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.ccr.2009.12.050
 Degree: -

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Title: Cancer Cell
  Other : Cancer Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 17 (4) Sequence Number: - Start / End Page: 400 - 411 Identifier: ISSN: 1535-6108
CoNE: https://pure.mpg.de/cone/journals/resource/111025129473004