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Fragment-based discovery of a chemical probe for the PWWP1 domain of NSD3.

Authors :
Böttcher J
Dilworth D
Reiser U
Neumüller RA
Schleicher M
Petronczki M
Zeeb M
Mischerikow N
Allali-Hassani A
Szewczyk MM
Li F
Kennedy S
Vedadi M
Barsyte-Lovejoy D
Brown PJ
Huber KVM
Rogers CM
Wells CI
Fedorov O
Rumpel K
Zoephel A
Mayer M
Wunberg T
Böse D
Zahn S
Arnhof H
Berger H
Reiser C
Hörmann A
Krammer T
Corcokovic M
Sharps B
Winkler S
Häring D
Cockcroft XL
Fuchs JE
Müllauer B
Weiss-Puxbaum A
Gerstberger T
Boehmelt G
Vakoc CR
Arrowsmith CH
Pearson M
McConnell DB
Source :
Nature chemical biology [Nat Chem Biol] 2019 Aug; Vol. 15 (8), pp. 822-829. Date of Electronic Publication: 2019 Jul 08.
Publication Year :
2019

Abstract

Here, we report the fragment-based discovery of BI-9321, a potent, selective and cellular active antagonist of the NSD3-PWWP1 domain. The human NSD3 protein is encoded by the WHSC1L1 gene located in the 8p11-p12 amplicon, frequently amplified in breast and squamous lung cancer. Recently, it was demonstrated that the PWWP1 domain of NSD3 is required for the viability of acute myeloid leukemia cells. To further elucidate the relevance of NSD3 in cancer biology, we developed a chemical probe, BI-9321, targeting the methyl-lysine binding site of the PWWP1 domain with sub-micromolar in vitro activity and cellular target engagement at 1 µM. As a single agent, BI-9321 downregulates Myc messenger RNA expression and reduces proliferation in MOLM-13 cells. This first-in-class chemical probe BI-9321, together with the negative control BI-9466, will greatly facilitate the elucidation of the underexplored biological function of PWWP domains.

Details

Language :
English
ISSN :
1552-4469
Volume :
15
Issue :
8
Database :
MEDLINE
Journal :
Nature chemical biology
Publication Type :
Academic Journal
Accession number :
31285596
Full Text :
https://doi.org/10.1038/s41589-019-0310-x