ArticleToxicology reports2025
MnTBAP, a peroxynitrite scavenger, attenuates cisplatin-induced apoptosis and cytotoxicity in organ of Corti cells.
Article in Toxicology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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1 citing paper in PubMed.
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5 authors.
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Abstract
Cisplatin, a widely used anti-cancer drug, induces apoptosis in cochlear hair cells. In previous studies, cisplatin-induced nitration and degradation of proteins such as LMO4 disrupted their anti-apoptotic signaling. Cotreatment with SRI110, a peroxynitrite decomposition catalyst, attenuated cisplatin-induced ototoxicity in rodents. However, it is not known if other compounds that target nitrative stress would also confer similar otoprotection. Manganese (III) tetrakis (4-benzoic acid) porphyrin (MnTBAP), a cell-permeable superoxide dismutase mimetic, is a peroxynitrite decomposition catalyst that selectively scavenges peroxynitrite. This study demonstrates that cotreatment of UB/OC1 cells MnTBAP prevented cisplatin-induced cytotoxicity and nitrative stress. Furthermore, the mRNA levels of pro-apoptotic genes such as
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