Pifithrin-μ Prevents Cisplatin-Induced Chemobrain by Preserving Neuronal Mitochondrial Function

Cancer Res. 2017 Feb 1;77(3):742-752. doi: 10.1158/0008-5472.CAN-16-1817. Epub 2016 Nov 22.

Abstract

Cognitive impairment, termed chemobrain, is a common neurotoxicity associated with chemotherapy treatment, affecting an estimated 78% of patients. Prompted by the hypothesis that neuronal mitochondrial dysfunction underlies chemotherapy-induced cognitive impairment (CICI), we explored the efficacy of administering the small-molecule pifithrin (PFT)-μ, an inhibitor of mitochondrial p53 accumulation, in preventing CICI. Male C57BL/6J mice injected with cisplatin ± PFT-μ for two 5-day cycles were assessed for cognitive function using novel object/place recognition and alternation in a Y-maze. Cisplatin impaired performance in the novel object/place recognition and Y-maze tests. PFT-μ treatment prevented CICI and associated cisplatin-induced changes in coherency of myelin basic protein fibers in the cingular cortex and loss of doublecortin+ cells in the subventricular zone and hippocampal dentate gyrus. Mechanistically, cisplatin decreased spare respirator capacity of brain synaptosomes and caused abnormal mitochondrial morphology, which was counteracted by PFT-μ administration. Notably, increased mitochondrial p53 did not lead to cerebral caspase-3 activation or cytochrome-c release. Furthermore, PFT-μ administration did not impair the anticancer efficacy of cisplatin and radiotherapy in tumor-bearing mice. Our results supported the hypothesis that neuronal mitochondrial dysfunction induced by mitochondrial p53 accumulation is an underlying cause of CICI and that PFT-μ may offer a tractable therapeutic strategy to limit this common side-effect of many types of chemotherapy. Cancer Res; 77(3); 742-52. ©2016 AACR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / toxicity*
  • Blotting, Western
  • Brain / drug effects*
  • Cisplatin / toxicity*
  • Cognition Disorders / chemically induced
  • Disease Models, Animal
  • Head and Neck Neoplasms / pathology
  • Male
  • Maze Learning / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Electron, Transmission
  • Mitochondria / drug effects
  • Neurons / drug effects*
  • Neuroprotective Agents / pharmacology*
  • Real-Time Polymerase Chain Reaction
  • Sulfonamides / pharmacology*
  • Tumor Suppressor Protein p53 / drug effects

Substances

  • 2-phenylacetylenesulfonamide
  • Antineoplastic Agents
  • Neuroprotective Agents
  • Sulfonamides
  • Tumor Suppressor Protein p53
  • Cisplatin