Back to Search Start Over

Progress in the Development of Lysine Methyltransferase SETD8 Inhibitors.

Authors :
Milite C
Feoli A
Viviano M
Rescigno D
Mai A
Castellano S
Sbardella G
Source :
ChemMedChem [ChemMedChem] 2016 Aug 19; Vol. 11 (16), pp. 1680-5. Date of Electronic Publication: 2016 Jul 14.
Publication Year :
2016

Abstract

SETD8/SET8/Pr-SET7/KMT5A is the only known lysine methyltransferase that monomethylates lysine 20 of histone H4 (H4K20) in vivo. The methyltransferase activity of SETD8 has been implicated in many essential cellular processes, including DNA replication, DNA damage response, transcription modulation, and cell cycle regulation. In addition to H4K20, SETD8 monomethylates non-histone substrates including proliferating cell nuclear antigen and p53. During the past decade, different structural classes of inhibitors targeting various lysine methyltransferases have been designed and developed. However, the development of SETD8 inhibitors is still in its infancy. This review covers the progress made to date in inhibiting the activity of SETD8 by small molecules, with an emphasis on their discovery, selectivity over other methyltransferases, and cellular activity.<br /> (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1860-7187
Volume :
11
Issue :
16
Database :
MEDLINE
Journal :
ChemMedChem
Publication Type :
Academic Journal
Accession number :
27411844
Full Text :
https://doi.org/10.1002/cmdc.201600272