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

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2024-12-27 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S480179
Xing Yang, Hengxiang Yu, Liming Zhou
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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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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。
目的:探讨氧化白藜芦醇(OXY)是否能减轻伊立替康(CPT-11)诱导的肠道毒性,两药联用是否能增强对结直肠癌细胞的抑制作用。方法:采用CCK-8法评估OXY和CPT-11单独或联合治疗对结直肠癌细胞系HCT116和SW620增殖的抑制作用。将小鼠(8只/组)分为对照组、CPT-11、低剂量OXY+CPT-11、高剂量OXY+CPT-11。每个试验都是作为一个独立的实验进行的。建立CPT-11致小鼠腹泻模型,观察各组小鼠一般情况、腹泻评分、脾脏和结肠的变化。利用生物信息学工具预测OXY和CPT-11的靶标,然后进行GO和KEGG富集分析。结果:CPT-11对结直肠癌细胞生长的抑制作用呈剂量依赖性,且OXY联合治疗具有叠加效应。CPT-11组小鼠出现了明显的体重减轻和严重的腹泻,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的靶点在PI3K/Akt和细胞周期等通路中富集,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联用增强了对结直肠肿瘤细胞的抑制作用,降低了CPT-11引起的肠道毒性。本研究为结直肠癌化疗提供了一种新的策略。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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