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Oxyresveratrol Alleviates Irinotecan-Induced Diarrhea and Enhances Antitumor Effects in Colorectal Cancer. | LitMetric

Oxyresveratrol Alleviates Irinotecan-Induced Diarrhea and Enhances Antitumor Effects in Colorectal Cancer.

Drug Des Devel Ther

West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, Sichuan, 610041, People's Republic of China.

Published: January 2025

AI Article Synopsis

  • The study explored if oxyresveratrol (OXY) can reduce the intestinal side effects of irinotecan (CPT-11) and improve its effectiveness against colorectal cancer.
  • OXY and CPT-11 were tested separately and together on colorectal cancer cell lines and in a mouse model, revealing that their combination enhances tumor cell growth inhibition while also alleviating CPT-11's adverse effects like diarrhea and weight loss.
  • The findings suggest that using OXY with CPT-11 could be a promising approach for colorectal cancer treatment by targeting specific biological pathways.

Article Abstract

Objective: To investigate whether oxyresveratrol (OXY) can alleviate irinotecan (CPT-11)-induced intestinal toxicity and whether the combination of these two drugs can enhance the inhibition of colorectal cancer cells.

Methods: The CCK-8 assay was used to assess the inhibitory effects of OXY and CPT-11, both as monotherapies and in combination, on the proliferation of colorectal cancer cell lines HCT116 and SW620. Mice were grouped (8/mice/group) into: control, CPT-11, low-dose OXY+CPT-11, high-dose OXY+CPT-11. Each trial was conducted as an independent experiment. A mouse diarrhea model induced by CPT-11 was established to observe the general condition, diarrhea score, spleen and colon of each group of mice. Bioinformatics tools were employed to predict the targets of OXY and CPT-11, followed by GO and KEGG enrichment analyses.

Results: CPT-11 inhibited the growth of colorectal cancer cells in a dose-dependent manner, and OXY combined treatment had additive effects. Mice in the CPT-11 group experienced significant weight loss and severe diarrhea, while the co-administration of OXY alleviated these adverse effects. Bioinformatics analysis revealed that the targets of OXY and CPT-11 were enriched in pathways such as PI3K/Akt and cell cycle, suggesting that the combination therapy might exert a synergistic effect by modulating these pathways.

Conclusion: The combination of OXY and CPT-11 enhances the inhibitory effect on colorectal tumor cells and reduces the intestinal toxicity induced by CPT-11. This study provides a novel strategy for colorectal cancer chemotherapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11687425PMC
http://dx.doi.org/10.2147/DDDT.S480179DOI Listing

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