AI Article Synopsis

  • Research explored a new herbal formula, MH-30, designed to enhance the efficacy of the chemotherapy drug cisplatin while reducing its toxicity on normal tissues.
  • In tests using mice with melanoma, MH-30 not only inhibited tumor growth on its own but also worked synergistically with cisplatin to enhance anticancer effects while improving immune response markers.
  • The combination treatment showed a significant reduction in cisplatin-induced toxic effects on liver and kidney function, suggesting that MH-30 may provide a safer alternative for cancer therapy.

Article Abstract

Background/aim: Although cisplatin is an effective anticancer drug, its toxic effects on normal tissues limit its use. We developed a herbal formula, MH-30, with increased fat-soluble polyphenols by improving the manufacturing method of HemoHIM. In this study, we examined whether the combination of MH-30 with cisplatin exerts synergistic antitumor effect while it reduces cisplatin-induced toxicities.

Materials And Methods: MH-30 was produced by adding the ethanol-insoluble fraction to its extract after decocting herbs in 30% ethanol and water. We used a melanoma-bearing mice model to investigate synergistic anticancer effects. The NK cell activity and cytokine levels were measured by Cr-release assay and ELISA. The AST, ALT, BUN, and creatinine levels were estimated in the serum.

Results: MH-30 effectively inhibited melanoma growth in vitro. Furthermore, MH-30 had a synergistic effect in combination with cisplatin on melanoma growth inhibition in vitro and in vivo. In melanoma-bearing mice, cisplatin alone decreased the activity of NK cells and the levels of IL-2 and IFN-γ, which were effectively restored by the combination of MH-30 with cisplatin. Combined treatment with MH-30 and cisplatin significantly inhibited the cisplatin-induced increase in the levels of AST, ALT, BUN, and creatinine.

Conclusion: Combination of MH-30 with cisplatin may be a beneficial anticancer treatment with reduced adverse effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439890PMC
http://dx.doi.org/10.21873/invivo.11979DOI Listing

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