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HDAC6 inhibition effectively reverses chemotherapy-induced peripheral neuropathy

2017; Elsevier BV; Volume: 66; Linguagem: Inglês

10.1016/j.bbi.2017.07.135

1090-2139

Jiacheng Ma, Karen Krukowski, Olga Golonzhka, Geoffroy Laumet, T. Gutti, John H. van Duzer, Ralph Mazitschek, Matthew Jarpe, Cobi J. Heijnen, Annemieke Kavelaars,

Multiple Myeloma Research and Treatments

Chemotherapy-induced peripheral neuropathy is one of the most common dose-limiting side-effects of cancer treatment. Currently, there is no FDA-approved treatment available. Histone deacetylase 6 (HDAC6) is a microtubule-associated deacetylase whose function includes regulation of α-tubulin- dependent intracellular mitochondrial transport. Here we examined the effect of HDAC6 inhibition on cisplatin-induced peripheral neuropathy. We used a novel HDAC6 inhibitor ACY-1083, which shows 260-fold selectivity towards HDAC6 versus other HDACs. Our results show that HDAC6 inhibition completely reversed already existing cisplatin-induced mechanical allodynia, spontaneous pain, and numbness. These findings were confirmed using the established HDAC6 inhibitor ACY-1215 (Ricolinostat), which is currently in clinical trials for cancer treatment. Mechanistically, treatment with the HDAC6 inhibitor increased α-tubulin acetylation in the peripheral nerve. In addition, HDAC6 inhibition restored the cisplatin-induced reduction in mitochondrial bioenergetics and mitochondrial content in the tibial nerve, indicating increased mitochondrial transport. At a later time point, dorsal root ganglion mitochondrial bioenergetics also improved. HDAC6 inhibition restored the loss of intra-epidermal nerve fiber density in cisplatin-treated mice. Our results demonstrate that pharmacological inhibition of HDAC6 completely reverses all the hallmarks of established cisplatin-induced peripheral neuropathy. These results are especially promising because one of the HDAC6 inhibitors tested here is currently in clinical trials as an add-on cancer therapy, highlighting the potential for a fast clinical translation of our findings.