TY - JOUR
T1 - Recent advances in the pharmacological targeting of ubiquitin-regulating enzymes in cancer
AU - Montagut, Ana Maria
AU - Armengol, Marc
AU - de Pablo, Gema Gorjón
AU - Estrada-Tejedor, Roger
AU - Borrell, José Ignacio
AU - Roué, Gaël
N1 - Funding Information:
This work has been co-financed by the European Regional Development Fund (ERDF) through the Interreg V-A Spain-France-Andorra (POCTEFA) program, project PROTEOblood (EFA360/19). G.R. acknowledges supports from Fondo de Investigación Sanitaria PI18/01383 (ERDF) “Una manera de hacer Europa”. This work was carried out under the CERCA Program (Generalitat de Catalunya).
Funding Information:
G. Roué received research funding from TG Therapeutics. The remaining authors have no competing financial interests.
Funding Information:
This work has been co-financed by the European Regional Development Fund (ERDF) through the Interreg V-A Spain-France-Andorra (POCTEFA) program, project PROTEOblood (EFA360/19). G.R. acknowledges supports from Fondo de Investigación Sanitaria PI18/01383 (ERDF) “Una manera de hacer Europa”. This work was carried out under the CERCA Program (Generalitat de Catalunya).
Publisher Copyright:
© 2022 The Authors
PY - 2022/12
Y1 - 2022/12
N2 - As a post-translational modification that has pivotal roles in protein degradation, ubiquitination ensures that intracellular proteins act in a precise spatial and temporal manner to regulate diversified cellular processes. Perturbation of the ubiquitin system contributes directly to the onset and progression of a wide variety of diseases, including various subtypes of cancer. This highly regulated system has been for years an active research area for drug discovery that is exemplified by several approved drugs. In this review, we will provide an update of the main breakthrough scientific discoveries that have been leading the clinical development of ubiquitin-targeting therapies in the last decade, with a special focus on E1 and E3 modulators. We will further discuss the unique challenges of identifying new potential therapeutic targets within this ubiquitous and highly complex machinery, based on available crystallographic structures, and explore chemical approaches by which these challenges might be met.
AB - As a post-translational modification that has pivotal roles in protein degradation, ubiquitination ensures that intracellular proteins act in a precise spatial and temporal manner to regulate diversified cellular processes. Perturbation of the ubiquitin system contributes directly to the onset and progression of a wide variety of diseases, including various subtypes of cancer. This highly regulated system has been for years an active research area for drug discovery that is exemplified by several approved drugs. In this review, we will provide an update of the main breakthrough scientific discoveries that have been leading the clinical development of ubiquitin-targeting therapies in the last decade, with a special focus on E1 and E3 modulators. We will further discuss the unique challenges of identifying new potential therapeutic targets within this ubiquitous and highly complex machinery, based on available crystallographic structures, and explore chemical approaches by which these challenges might be met.
KW - Cancer
KW - Clinical trial
KW - Deubiquitinase
KW - Preclinical screening
KW - Structure-based drug design
KW - Ubiquitin ligase
UR - http://www.scopus.com/inward/record.url?scp=85124823522&partnerID=8YFLogxK
U2 - 10.1016/j.semcdb.2022.02.007
DO - 10.1016/j.semcdb.2022.02.007
M3 - Review
C2 - 35184940
AN - SCOPUS:85124823522
SN - 1084-9521
VL - 132
SP - 213
EP - 229
JO - Seminars in Cell and Developmental Biology
JF - Seminars in Cell and Developmental Biology
ER -