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GSTA4 mediates reduction of cisplatin ototoxicity in female mice.

Nature communications | 2019

Cisplatin is one of the most widely used chemotherapeutic drugs for the treatment of cancer. Unfortunately, one of its major side effects is permanent hearing loss. Here, we show that glutathione transferase α4 (GSTA4), a member of the Phase II detoxifying enzyme superfamily, mediates reduction of cisplatin ototoxicity by removing 4-hydroxynonenal (4-HNE) in the inner ears of female mice. Under cisplatin treatment, loss of Gsta4 results in more profound hearing loss in female mice compared to male mice. Cisplatin stimulates GSTA4 activity in the inner ear of female wild-type, but not male wild-type mice. In female Gsta4-/- mice, cisplatin treatment results in increased levels of 4-HNE in cochlear neurons compared to male Gsta4-/- mice. In CBA/CaJ mice, ovariectomy decreases mRNA expression of Gsta4, and the levels of GSTA4 protein in the inner ears. Thus, our findings suggest that GSTA4-dependent detoxification may play a role in estrogen-mediated neuroprotection.

Pubmed ID: 31515474 RIS Download

Associated grants

  • Agency: NIDCD NIH HHS, United States
    Id: R01 DC012552
  • Agency: NIA NIH HHS, United States
    Id: R01 AG037984
  • Agency: NIDCD NIH HHS, United States
    Id: R01 DC014437
  • Agency: NIDCD NIH HHS, United States
    Id: R03 DC011840
  • Agency: NIA NIH HHS, United States
    Id: P30 AG028740
  • Agency: NCRR NIH HHS, United States
    Id: C06 RR029852

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