Related Experiment Video
Updated: Feb 20, 2026

Cell Subtype-specific Analysis of Neuronal Membrane Proteasome in Somatosensory Neurons
Published on: October 10, 2025
An Overview of Bortezomib-Induced Neurotoxicity
1Experimental Neurology Unit, Department of Surgery and Translational Medicine, University of Milan-Bicocca, Via Cadore 48, 20900 Monza (MB), Italy. cristina.meregalli@unimib.it.
Abstract:
The boronic acid dipeptide bortezomib, able to induce tumor cell death by degradation of key proteins, is the first proteasome inhibitor drug to enter clinical practice. It is employed as first-line treatment in relapsed or resistant multiple myeloma (MM) patients. However, bortezomib often induces a dose-limiting toxicity in the form of painful sensory neuropathy, which can mainly be reduced by subcutaneous administration or dose modification. In this review we focus on the current understanding of the pathophysiological mechanisms of bortezomib-induced neuropathy to allow further studies in animal models and humans, including analysis of clinical and pharmacogenetic aspects, to optimize the treatment regimens.
Insights
Bortezomib, a proteasome inhibitor, treats multiple myeloma but causes painful neuropathy. Understanding its mechanisms is key to optimizing treatment and reducing side effects in patients.
Area of Science:
- Oncology
- Pharmacology
- Neuroscience
Background:
- Bortezomib is a proteasome inhibitor used for multiple myeloma.
- It induces tumor cell death by degrading key proteins.
- Bortezomib is the first proteasome inhibitor in clinical practice.
Purpose of the Study:
- To review the pathophysiological mechanisms of bortezomib-induced neuropathy.
- To analyze clinical and pharmacogenetic aspects of bortezomib neuropathy.
- To optimize treatment regimens for multiple myeloma patients.
Main Methods:
- Review of current literature on bortezomib-induced neuropathy.
- Analysis of clinical data and pharmacogenetic studies.
- Discussion of animal models and human studies.
Main Results:
- Bortezomib-induced neuropathy is a dose-limiting toxicity.
- Subcutaneous administration or dose modification can reduce neuropathy.
- Understanding mechanisms is crucial for optimizing treatment.
Conclusions:
- Further research into bortezomib neuropathy mechanisms is needed.
- Clinical and pharmacogenetic analysis can guide treatment optimization.
- Optimized regimens will improve patient outcomes in multiple myeloma.
Related Concept Videos
Drug Toxicity: Overview
Drug Toxicity: Risk factors
Drug Toxicity: Dose-Dependent Reactions
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists
Drug toxicity: Idiosyncratic Reactions
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists
Phenothiazines, such as prochlorperazine...

