TY - JOUR
T1 - Drug Discovery Targeting Nuclear Receptor Binding SET Domain Protein 2 (NSD2)
AU - Ma, Zonghui
AU - Bolinger, Andrew A.
AU - Chen, Haiying
AU - Zhou, Jia
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/8/24
Y1 - 2023/8/24
N2 - Nuclear receptor binding SET domain proteins (NSDs) catalyze the mono- or dimethylation of histone 3 lysine 36 (H3K36me1 and H3K36me2), using S-adenosyl-l-methionine (SAM) as a methyl donor. As a key member of the NSD family of proteins, NSD2 plays an important role in the pathogenesis and progression of various diseases such as cancers, inflammations, and infectious diseases, serving as a promising drug target. Developing potent and specific NSD2 inhibitors may provide potential novel therapeutics. Several NSD2 inhibitors and degraders have been discovered while remaining in the early stage of drug development. Excitingly, KTX-1001, a selective NSD2 inhibitor, has entered clinical trials. In this Perspective, the structures and functions of NSD2, its roles in various human diseases, and the recent advances in drug discovery strategies targeting NSD2 have been summarized. The challenges, opportunities, and future directions for developing NSD2 inhibitors and degraders are also discussed.
AB - Nuclear receptor binding SET domain proteins (NSDs) catalyze the mono- or dimethylation of histone 3 lysine 36 (H3K36me1 and H3K36me2), using S-adenosyl-l-methionine (SAM) as a methyl donor. As a key member of the NSD family of proteins, NSD2 plays an important role in the pathogenesis and progression of various diseases such as cancers, inflammations, and infectious diseases, serving as a promising drug target. Developing potent and specific NSD2 inhibitors may provide potential novel therapeutics. Several NSD2 inhibitors and degraders have been discovered while remaining in the early stage of drug development. Excitingly, KTX-1001, a selective NSD2 inhibitor, has entered clinical trials. In this Perspective, the structures and functions of NSD2, its roles in various human diseases, and the recent advances in drug discovery strategies targeting NSD2 have been summarized. The challenges, opportunities, and future directions for developing NSD2 inhibitors and degraders are also discussed.
UR - http://www.scopus.com/inward/record.url?scp=85168785567&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85168785567&partnerID=8YFLogxK
U2 - 10.1021/acs.jmedchem.3c00948
DO - 10.1021/acs.jmedchem.3c00948
M3 - Review article
C2 - 37578463
AN - SCOPUS:85168785567
SN - 0022-2623
VL - 66
SP - 10991
EP - 11026
JO - Journal of medicinal chemistry
JF - Journal of medicinal chemistry
IS - 16
ER -