| Literature DB >> 33415008 |
Xiaodong Tan1, Yingjie Zhou2, Aditi Agarwal1, Michelle Lim1, Yingyue Xu1, Yueming Zhu3, Joseph O'Brien3, Elizabeth Tran3, Jing Zheng1,2,4, David Gius5, Claus-Peter Richter1,2,4,6.
Abstract
Cisplatin is a potent drug used in about 40% of cancer treatment but also leads to severe deafness in 60-80% of the cases. Although the mechanism is known to be related to the accumulation of reactive oxygen species (ROS), no drug or FDA approved treatment is currently available to prevent cisplatin ototoxicity. With this study, we show for the first time that honokiol (HNK), a pleiotropic poly-phenol prevents cisplatin-induced hearing loss. HNK also improves the wellbeing of the mice during the treatment, determined by the increase in the number of surviving animals. In a transgenic tumor mouse model, HNK does not hinder cisplatin's antitumor effect. The mechanism is related to the activation of sirtuin 3, a deacetylase in mitochondria essential for ROS detoxification. We expect a paradigm shift in cisplatin chemotherapy based on the current study and future clinical trials, where honokiol is applied to reduce side effects including hearing loss. AJCREntities:
Keywords: Chemotherapy; cochlea; hearing protection; reactive oxygen species; tumor-bearing mice
Year: 2020 PMID: 33415008 PMCID: PMC7783741
Source DB: PubMed Journal: Am J Cancer Res ISSN: 2156-6976 Impact factor: 6.166