Metal drugs and the anticancer immune response

B Englinger, C Pirker, P Heffeter, A Terenzi… - Chemical …, 2018 - ACS Publications
The immune system deploys a multitude of innate and adaptive mechanisms not only to
ward off pathogens but also to prevent malignant transformation (“immune surveillance”) …

USP14: structure, function, and target inhibition

F Wang, S Ning, B Yu, Y Wang - Frontiers in Pharmacology, 2022 - frontiersin.org
Ubiquitin-specific protease 14 (USP14), a deubiquitinating enzyme (DUB), is associated
with proteasomes and exerts a dual function in regulating protein degradation. USP14 …

The AUTOTAC chemical biology platform for targeted protein degradation via the autophagy-lysosome system

CH Ji, HY Kim, MJ Lee, AJ Heo, DY Park, S Lim… - Nature …, 2022 - nature.com
Targeted protein degradation allows targeting undruggable proteins for therapeutic
applications as well as eliminating proteins of interest for research purposes. While several …

Advances in the development ubiquitin-specific peptidase (USP) inhibitors

S Chen, Y Liu, H Zhou - International journal of molecular sciences, 2021 - mdpi.com
Ubiquitylation and deubiquitylation are reversible protein post-translational modification
(PTM) processes involving the regulation of protein degradation under physiological …

Broad spectrum deubiquitinase inhibition induces both apoptosis and ferroptosis in cancer cells

L Yang, X Chen, Q Yang, J Chen, Q Huang… - Frontiers in …, 2020 - frontiersin.org
Proteasomal deubiquitinase (DUB) inhibition has been found to be effective in experimental
cancer therapy by inducing proteasome inhibition and apoptosis. Ferroptosis is a form of …

The proteasome as a druggable target with multiple therapeutic potentialities: Cutting and non-cutting edges

GR Tundo, D Sbardella, AM Santoro, A Coletta… - Pharmacology & …, 2020 - Elsevier
Abstract Ubiquitin Proteasome System (UPS) is an adaptable and finely tuned system that
sustains proteostasis network under a large variety of physiopathological conditions. Its …

The mechanism of tumour cell death by metal-based anticancer drugs is not only a matter of DNA interactions

A Bergamo, PJ Dyson, G Sava - Coordination Chemistry Reviews, 2018 - Elsevier
Platinum drugs are extensively used in the clinic to treat cancer, often leading to a palliative
response rather than a cure. While DNA is considered to be the primary target of platinum …

Targeting the ubiquitin-proteasome system for cancer treatment: discovering novel inhibitors from nature and drug repurposing

CL Soave, T Guerin, J Liu, QP Dou - Cancer and Metastasis Reviews, 2017 - Springer
In the past 15 years, the proteasome has been validated as an anti-cancer drug target and
20S proteasome inhibitors (such as bortezomib and carfilzomib) have been approved by the …

Gold nanoparticles induced size dependent cytotoxicity on human alveolar adenocarcinoma cells by inhibiting the ubiquitin proteasome system

B Ibrahim, TH Akere, S Chakraborty, E Valsami-Jones… - Pharmaceutics, 2023 - mdpi.com
Gold nanoparticles (AuNPs) are widely used in biomedicine due to their remarkable
therapeutic applications. However, little is known about their cytotoxic effects on the ubiquitin …

The deubiquitylase UCHL3 maintains cancer stem-like properties by stabilizing the aryl hydrocarbon receptor

L Ouyang, B Yan, Y Liu, C Mao, M Wang… - … and Targeted Therapy, 2020 - nature.com
Cancer stem cells (CSCs) exhibit highly aggressive and metastatic features and resistance
to chemotherapy and radiotherapy. Aryl hydrocarbon receptor (AhR) expression varies …