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Deconvolution of Buparlisib’s mechanism of action defines specific PI3K and tubulin inhibitors for therapeutic intervention

Authors :
Thomas Bohnacker
Andrea E. Prota
Florent Beaufils
John E. Burke
Anna Melone
Alison J. Inglis
Denise Rageot
Alexander M. Sele
Vladimir Cmiljanovic
Natasa Cmiljanovic
Katja Bargsten
Amol Aher
Anna Akhmanova
J. Fernando Díaz
Doriano Fabbro
Marketa Zvelebil
Roger L. Williams
Michel O. Steinmetz
Matthias P. Wymann
Source :
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
Publication Year :
2017
Publisher :
Nature Portfolio, 2017.

Abstract

Buparlisib/BKM120 is in phase 3 clinical trials as a phosphoinositide 3-kinase (PI3K) inhibitor. Here, Bohnackeret al. combine chemical biology and structural biology approaches to segregate BKM120’s biological actions, and suggest that it causes mitotic arrest predominantly by binding microtubules and disrupting their dynamics.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
8
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.5212909a4a7490db4d79600c172c822
Document Type :
article
Full Text :
https://doi.org/10.1038/ncomms14683