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Combinatorial Chemistry & High Throughput Screening

Editor-in-Chief

ISSN (Print): 1386-2073
ISSN (Online): 1875-5402

Review Article

Mechanistic Involvement of Inflammation in Bortezomib-induced Peripheral Neuropathy

Author(s): Lavisha Goel, Pooja Gupta* and Monika Pahuja

Volume 25, Issue 10, 2022

Published on: 22 July, 2022

Page: [1595 - 1600] Pages: 6

DOI: 10.2174/1386207325666220524144147

Price: $65

Abstract

Aim: The aim of the study was to establish the role of inflammation in bortezomibinduced peripheral neuropathy (BIPN).

Background: Peripheral neuropathy is the dose-limiting toxicity of bortezomib that can lead to discontinuation of the treatment. There are multiple mechanisms involved in the disposition of BIPN. However, the role of inflammatory mediators is still under investigation. A complete understanding of inflammatory markers in relation to BIPN can lead to the development of effective therapy for prophylaxis and treatment of peripheral neuropathy.

Objective: Based on the available data, the role of inflammatory mediators in the development of peripheral neuropathy due to bortezomib has been postulated.

Methods: The “Pubmed” and “Google Scholar” were used as the search engines with terms like “peripheral neuropathy”, “bortezomib-induced peripheral neuropathy” and “inflammation”. Original research, case reports and review articles were considered.

Results: Bortezomib use is associated with the development of peripheral neuropathy. This effect is due to the damage to Schwann cells and dorsal root ganglion neurons, mitochondrial damage, increased ion channel susceptibility, and higher infiltration of macrophages in the spinal cord. All these factors collectively increase the secretion of inflammatory mediators and lead to the development of neuropathic pain.

Conclusion: Targeting inflammatory mediators may be helpful in the treatment of bortezomibinduced peripheral neuropathy.

Keywords: Bortezomib, peripheral neuropathy, inflammatory mediators, Schwann cells, tumor necrosis factor-alpha, myeloma.

Graphical Abstract

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