Preventing neuropathy and improving anticancer chemotherapy with a carbazole-based compound

While advances in cancer therapy have improved remission rates, chemotherapy-induced peripheral neuropathy (CIPN) remains a lasting and untreatable side effect. This study introduces Carba1, a bifunctional carbazole compound that protects against CIPN through two mechanisms. First, Carba1 interacts with tubulin, allowing for lower doses of taxanes, common chemotherapeutics known for causing CIPN, without reducing their anticancer effectiveness. Second, Carba1 activates nicotinamide phosphoribosyltransferase (NAMPT), enhancing NAD biosynthesis and boosting the metabolic resilience of neurons and Schwann cells against chemotherapy-induced damage. Carba1 shows strong neuroprotective effects in vitro against paclitaxel, cisplatin, and bortezomib toxicity and in vivo in a rat model of paclitaxel-induced neuropathy. Crucially, Carba1 does not interfere with paclitaxel's tumor-fighting ability or promote tumor growth. Structure-activity analyses of Carba1 derivatives reveal the potential to develop compounds with dual or solely neuroprotective effects. These findings position Carba1 as a promising candidate to prevent CIPN, with potential to enhance both cancer treatment outcomes and patients' quality of life.

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Publication Details

Journal
Science Advances
Published
2025-10-29
DOI
https://doi.org/10.1126/sciadv.adw6328
Citations
1
Primary Topic
Cancer Treatment and Pharmacology
Type
article
Field-Weighted Citation Impact
1.05
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article

Preventing neuropathy and improving anticancer chemotherapy with a carbazole-based compound

Uwe Schlattner, Peggy Suzanne, Sophie Michallet, Bénédicte Elena‐Herrmann et al.
1 citations
Science Advances
Cancer Treatment and Pharmacology
1.05
article

Preventing neuropathy and improving anticancer chemotherapy with a carbazole-based compound

Uwe Schlattner, Peggy Suzanne, Sophie Michallet, Bénédicte Elena‐Herrmann, David Balayssac, Francesca Bartolini, Chantal Thibert, Patrick Dallemagne, Joran Villaret, Jordan Allard, A. Mercier, Julien Vollaire, Lauriane Bosc, Nathalie Jacquemot, Laurence Lafanéchère, Véronique Josserand, Cécile Cottet‐Rousselle, Sakina Torch, Maria Elena Pero, Sumari Marais
article en
1 citations

Abstract

While advances in cancer therapy have improved remission rates, chemotherapy-induced peripheral neuropathy (CIPN) remains a lasting and untreatable side effect. This study introduces Carba1, a bifunctional carbazole compound that protects against CIPN through two mechanisms. First, Carba1 interacts with tubulin, allowing for lower doses of taxanes, common chemotherapeutics known for causing CIPN, without reducing their anticancer effectiveness. Second, Carba1 activates nicotinamide phosphoribosyltransferase (NAMPT), enhancing NAD biosynthesis and boosting the metabolic resilience of neurons and Schwann cells against chemotherapy-induced damage. Carba1 shows strong neuroprotective effects in vitro against paclitaxel, cisplatin, and bortezomib toxicity and in vivo in a rat model of paclitaxel-induced neuropathy. Crucially, Carba1 does not interfere with paclitaxel's tumor-fighting ability or promote tumor growth. Structure-activity analyses of Carba1 derivatives reveal the potential to develop compounds with dual or solely neuroprotective effects. These findings position Carba1 as a promising candidate to prevent CIPN, with potential to enhance both cancer treatment outcomes and patients' quality of life.

Science AdvancesVol. 11(44)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Institut Universitaire de France (FR), University of Clermont Auvergne (FR), Normandie Université (FR), Centre Hospitalier Universitaire de Clermont-Ferrand (FR), Clermont Université (FR), Laboratory of Fundamental and Applied Bioenergetics (FR), Institut pour l'avancée des biosciences (FR), University of Pretoria (ZA), University of Naples Federico II (IT), Columbia University (US), Université Grenoble Alpes (FR), Université de Caen Normandie (FR)
Openalex Percentile: Top 16%
Cancer Treatment and Pharmacology
1.05
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