Key result
Glycine max and Chrysanthemum indicum extracts protected human proximal tubular cells against cisplatin-induced apoptosis via antioxidant activity without interfering with toxicity in cancer cells.
Glycine max and Chrysanthemum indicum extracts show potential as nephroprotective agents against cisplatin-induced toxicity without compromising its anti-cancer efficacy.
May support adjunctive nephroprotection with cisplatin; hypothesis-generating and requires clinical validation before practice change.
UNLABELLED: Although cisplatin is one of the most efficient chemotherapeutic agents for the treatment of solid tumors, frequently observed nephrotoxicity has limited its use in several patients. MATERIALS AND METHODS: The protective effect of Glycine max (GM) and Chrysanthemum indicum (CM) extracts on cisplatin-induced apoptosis in human proximal tubular HK-2 cells was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), Hoechst 33342, and propidium iodide assays. Reactive oxygen species (ROS) were determined by flow cytometry with 2,7-dichlorofluorescein diacetate (DCFH(2)-DA). RESULTS: Cisplatin-induced renal cell toxicity through the induction of hydrogen peroxide (H(2)O(2)) and hydroxyl radical (OH(•-)). CM extract protected cisplatin-induced apoptosis by its anti-oxidant activity against H(2)O(2) and OH(•-), while GM extract scavenged only H(2)O(2). Furthermore, GM and CM extracts protect renal cells without significant interfering effect on cisplatin toxicity in lung cancer H460 and melanoma G361 cells. CONCLUSION: GM and CM extracts exhibited a promising protective effect on cisplatin-induced nephrotoxicity which could benefit the development for nephroprotective approaches.
No takes yet. Share an insight, caveat, or question.
Pongjit et al. (2011) studied Cisplatin-induced nephrotoxicity. Glycine max and Chrysanthemum indicum extracts was evaluated on Cisplatin-induced apoptosis in human proximal tubular HK-2 cells. Glycine max and Chrysanthemum indicum extracts protected human proximal tubular cells against cisplatin-induced apoptosis via antioxidant activity without interfering with toxicity in cancer cells.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: