Pharmacokinetics and pharmacokinetic–pharmacodynamic correlations of therapeutic peptides

L Diao, B Meibohm - Clinical pharmacokinetics, 2013 - Springer
Peptides, defined as polymers of less than 50 amino acids with a molecular weight of less
than 10 kDa, represent a fast-growing class of new therapeutics which has unique …

[HTML][HTML] Bortezomib for the treatment of hematologic malignancies: 15 years later

P Robak, T Robak - Drugs in R&D, 2019 - Springer
Bortezomib is a dipeptidyl boronic acid that selectively inhibits the ubiquitin proteasome
pathway, which plays a role in the degradation of many intracellular proteins. It is the first-in …

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 …

[HTML][HTML] Hepatotoxicity secondary to chemotherapy

A Grigorian, CB O'Brien - Journal of clinical and translational …, 2014 - ncbi.nlm.nih.gov
The difficult problem faced by multiple generation of practicing physicians is determining the
cause of abnormal liver function tests in cancer patients on chemotherapy. Hepatotoxicity …

Current approaches to management of newly diagnosed multiple myeloma

U Goel, S Usmani, S Kumar - American journal of hematology, 2022 - Wiley Online Library
Major developments in the treatment of multiple myeloma (MM) over the past decade have
led to a continued improvement in survival. Significant progress has been made with deeper …

Clinical pharmacokinetics and pharmacodynamics of bortezomib

CRC Tan, S Abdul-Majeed, B Cael, SK Barta - Clinical pharmacokinetics, 2019 - Springer
Proteasome inhibitors disrupt multiple pathways in cells and the bone marrow
microenvironment, resulting in apoptosis and inhibition of cell-cycle progression …

Oral anticancer drugs: mechanisms of low bioavailability and strategies for improvement

FE Stuurman, B Nuijen, JH Beijnen… - Clinical …, 2013 - Springer
The use of oral anticancer drugs has increased during the last decade, because of patient
preference, lower costs, proven efficacy, lack of infusion-related inconveniences, and the …

[HTML][HTML] Progress on the application of bortezomib and bortezomib-based nanoformulations

J Liu, R Zhao, X Jiang, Z Li, B Zhang - Biomolecules, 2021 - mdpi.com
Bortezomib (BTZ) is the first proteasome inhibitor approved by the Food and Drug
Administration. It can bind to the amino acid residues of the 26S proteasome, thereby …

Pharmacokinetics and pharmacodynamics of nab‐paclitaxel in patients with solid tumors: Disposition kinetics and pharmacology distinct from solvent‐based …

N Chen, Y Li, Y Ye, M Palmisano… - The Journal of …, 2014 - Wiley Online Library
The aim of this study was to characterize population pharmacokinetics and the exposure–
neutropenia relationship with nanoparticle albumin‐bound (nab)‐paclitaxel in patients with …

Proteasome inhibition in combination with immunotherapies: State-of-the-Art in multiple myeloma

D Kegyes, D Gulei, R Drula, D Cenariu, B Tigu, D Dima… - Blood Reviews, 2023 - Elsevier
Multiple myeloma (MM) is a malignant plasma cell disorder accounting for around 1.8% of
all neoplastic diseases. Nowadays, clinicians have a broad arsenal of drugs at their disposal …