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氧化白藜芦醇减轻伊立替康诱导的腹泻并增强结直肠癌的抗肿瘤作用。

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

作者信息

Yang Xing, Yu Hengxiang, Zhou Liming

机构信息

School of Pharmacy, North Sichuan Medical College, Nanchong, Sichuan, 637600, People's Republic of China.

The Fourth People's Hospital of Nanchong, Nanchong, Sichuan, 637600, People's Republic of China.

出版信息

Drug Des Devel Ther. 2024 Dec 27;18:6283-6295. doi: 10.2147/DDDT.S480179. eCollection 2024.

DOI:10.2147/DDDT.S480179
PMID:39741919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11687425/
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.

摘要

目的

研究氧化白藜芦醇(OXY)是否能减轻伊立替康(CPT-11)诱导的肠道毒性,以及这两种药物联合使用是否能增强对结肠癌细胞的抑制作用。

方法

采用CCK-8法评估OXY和CPT-11单药及联合用药对结肠癌细胞系HCT116和SW620增殖的抑制作用。将小鼠(8只/组)分为:对照组、CPT-11组、低剂量OXY+CPT-11组、高剂量OXY+CPT-11组。每项试验均作为独立实验进行。建立CPT-11诱导的小鼠腹泻模型,观察各组小鼠的一般状况、腹泻评分、脾脏和结肠情况。利用生物信息学工具预测OXY和CPT-11的靶点,随后进行GO和KEGG富集分析。

结果

CPT-11以剂量依赖方式抑制结肠癌细胞生长,OXY联合治疗具有相加作用。CPT-11组小鼠体重显著减轻且腹泻严重,而OXY联合给药减轻了这些不良反应。生物信息学分析显示,OXY和CPT-11的靶点富集于PI3K/Akt和细胞周期等通路,提示联合治疗可能通过调节这些通路发挥协同作用。

结论

OXY与CPT-11联合使用增强了对结肠肿瘤细胞的抑制作用,并降低了CPT-11诱导的肠道毒性。本研究为结肠癌化疗提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/cc3f562c950f/DDDT-18-6283-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/3272010fcc82/DDDT-18-6283-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/950e3b664598/DDDT-18-6283-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/a5ea6c319e7d/DDDT-18-6283-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/e351fbb2a5ef/DDDT-18-6283-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/cc3f562c950f/DDDT-18-6283-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/3272010fcc82/DDDT-18-6283-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/950e3b664598/DDDT-18-6283-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/a5ea6c319e7d/DDDT-18-6283-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/e351fbb2a5ef/DDDT-18-6283-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece2/11687425/cc3f562c950f/DDDT-18-6283-g0005.jpg

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