A practical review of proteasome pharmacology

TA Thibaudeau, DM Smith - Pharmacological reviews, 2019 - ASPET
The ubiquitin proteasome system (UPS) degrades individual proteins in a highly regulated
fashion and is responsible for the degradation of misfolded, damaged, or unneeded cellular …

The emerging roles of HDACs and their therapeutic implications in cancer

R Hai, D Yang, F Zheng, W Wang, X Han… - European Journal of …, 2022 - Elsevier
Deregulation of protein post-translational modifications is intensively involved in the etiology
of diseases, including degenerative diseases, inflammatory injuries, and cancers …

MIR145-3p promotes autophagy and enhances bortezomib sensitivity in multiple myeloma by targeting HDAC4

H Wu, C Liu, Q Yang, C Xin, J Du, F Sun, L Zhou - Autophagy, 2020 - Taylor & Francis
Multiple myeloma (MM) is an incurable plasma cell malignancy with poor survival.
Autophagy, a stress-responsive catabolic process mediated by lysosomal activity, plays a …

Indatuximab ravtansine (BT062) monotherapy in patients with relapsed and/or refractory multiple myeloma

S Jagannath, LT Heffner Jr, S Ailawadhi… - … Myeloma and Leukemia, 2019 - Elsevier
Background Indatuximab ravtansine (BT062) is an antibody-drug conjugate that binds to
CD138, which is overexpressed on multiple myeloma (MM) cells. Patients and Methods We …

Revisiting proteasome inhibitors: molecular underpinnings of their development, mechanisms of resistance and strategies to overcome anti-cancer drug resistance

C Leonardo-Sousa, AN Carvalho, RA Guedes… - Molecules, 2022 - mdpi.com
Proteasome inhibitors have shown relevant clinical activity in several hematological
malignancies, namely in multiple myeloma and mantle cell lymphoma, improving patient …

Bortezomib treatment modulates autophagy in multiple myeloma

G Di Lernia, P Leone, AG Solimando… - Journal of clinical …, 2020 - mdpi.com
Although the introduction of bortezomib as a therapeutic strategy has improved the overall
survival of multiple myeloma (MM) patients, 15–20% of high-risk patients do not respond to …

Blocking autophagy overcomes resistance to dual histone deacetylase and proteasome inhibition in gynecologic cancer

J Bi, Y Zhang, PK Malmrose, HA Losh… - Cell death & …, 2022 - nature.com
Histone deacetylase (HDAC) inhibitors and proteasome inhibitors have been approved by
the FDA for the treatment of multiple myeloma and lymphoma, respectively, but have not …

The role of deubiquitinating enzymes in cancer drug resistance

P Tanguturi, KS Kim, S Ramakrishna - Cancer chemotherapy and …, 2020 - Springer
Drug resistance is a well-known phenomenon leading to a reduction in the effectiveness of
pharmaceutical treatments. Resistance to chemotherapeutic agents can involve various …

Phase I study of the anti-FcRH5 antibody-drug conjugate DFRF4539A in relapsed or refractory multiple myeloma

AK Stewart, AY Krishnan, S Singhal, RV Boccia… - Blood cancer …, 2019 - nature.com
FcRH5 is a cell surface marker enriched on malignant plasma cells when compared to other
hematologic malignancies and normal tissues. DFRF4539A is an anti-FcRH5 antibody-drug …

HDAC6 degradation inhibits the growth of high-grade serous ovarian cancer cells

A Ali, F Zhang, A Maguire, T Byrne, K Weiner-Gorzel… - Cancers, 2020 - mdpi.com
Simple Summary The objective of this study was, firstly, to investigate the relationship
between Histone deacetylase 6 (HDAC6) expression and survival in patients with ovarian …