HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Discovery of a first-in-class reversible DNMT1-selective inhibitor with improved tolerability and efficacy in acute myeloid leukemia.

Abstract
DNA methylation, a key epigenetic driver of transcriptional silencing, is universally dysregulated in cancer. Reversal of DNA methylation by hypomethylating agents, such as the cytidine analogs decitabine or azacytidine, has demonstrated clinical benefit in hematologic malignancies. These nucleoside analogs are incorporated into replicating DNA where they inhibit DNA cytosine methyltransferases DNMT1, DNMT3A and DNMT3B through irreversible covalent interactions. These agents induce notable toxicity to normal blood cells thus limiting their clinical doses. Herein we report the discovery of GSK3685032, a potent first-in-class DNMT1-selective inhibitor that was shown via crystallographic studies to compete with the active-site loop of DNMT1 for penetration into hemi-methylated DNA between two CpG base pairs. GSK3685032 induces robust loss of DNA methylation, transcriptional activation and cancer cell growth inhibition in vitro. Due to improved in vivo tolerability compared with decitabine, GSK3685032 yields superior tumor regression and survival mouse models of acute myeloid leukemia.
AuthorsMelissa B Pappalardi, Kathryn Keenan, Mark Cockerill, Wendy A Kellner, Alexandra Stowell, Christian Sherk, Kristen Wong, Sarath Pathuri, Jacques Briand, Michael Steidel, Philip Chapman, Arthur Groy, Ashley K Wiseman, Charles F McHugh, Nino Campobasso, Alan P Graves, Emma Fairweather, Thilo Werner, Ali Raoof, Roger J Butlin, Lourdes Rueda, John R Horton, David T Fosbenner, Cunyu Zhang, Jessica L Handler, Morris Muliaditan, Makda Mebrahtu, Jon-Paul Jaworski, Dean E McNulty, Charlotte Burt, H Christian Eberl, Amy N Taylor, Thau Ho, Susan Merrihew, Shawn W Foley, Anna Rutkowska, Mei Li, Stuart P Romeril, Kristin Goldberg, Xing Zhang, Christopher S Kershaw, Marcus Bantscheff, Anthony J Jurewicz, Elisabeth Minthorn, Paola Grandi, Mehul Patel, Andrew B Benowitz, Helai P Mohammad, Aidan G Gilmartin, Rab K Prinjha, Donald Ogilvie, Christopher Carpenter, Dirk Heerding, Stephen B Baylin, Peter A Jones, Xiaodong Cheng, Bryan W King, Juan I Luengo, Allan M Jordan, Ian Waddell, Ryan G Kruger, Michael T McCabe
JournalNature cancer (Nat Cancer) Vol. 2 Issue 10 Pg. 1002-1017 (10 2021) ISSN: 2662-1347 [Electronic] England
PMID34790902 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Decitabine
  • DNA
  • DNA Modification Methylases
  • Azacitidine
Topics
  • Animals
  • Azacitidine (pharmacology)
  • DNA (metabolism)
  • DNA Methylation
  • DNA Modification Methylases (genetics)
  • Decitabine (pharmacology)
  • Leukemia, Myeloid, Acute (drug therapy)
  • Mice

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: