伐地那非、利格列汀联合伊立替康脂质体协同治疗结直肠癌。

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Xian Zhao, Ruijie Xu, Yuanyuan Zhai, Yi Wang, Yuxin Zhang, Yuan Tian, Fengguo Xu, Pei Zhang
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引用次数: 0

摘要

背景:伊立替康(CPT-11)是结直肠癌(CRC)的标准一线化疗药物。然而,其临床应用往往存在胃肠道毒性和治疗效果有限的问题。我们之前的研究表明,伐地那非(Vard)和利格列汀(Linag)联合使用可显著减轻cpt -11诱导的体外和体内模型肠道毒性。目前尚不清楚这种组合是否能协同增强CPT-11的抗癌活性。方法:通过对CRC细胞系HCT116、SW620和HT29的细胞活力测定,评估Vard、Linag和CPT-11的体外协同作用。建立了活体异种移植小鼠模型,以评估Vard和Linag原体和脂质体形式联合CPT-11的药物疗效。此外,非靶向代谢组学被用于探索观察到的协同效应的潜在机制。结果:在体外,Vard和Linag联合使用可协同增强CPT-11在结直肠癌细胞系中的抗癌活性。在体内,Vard和Linag的脂质体制剂倾向于在肿瘤部位积聚,提高药物靶向性,协同增强CPT-11的抗癌功效。非靶向代谢组学分析显示,这种协同作用可能是通过调节溶血磷脂代谢介导的。结论:Vard和Linag脂质体联合CPT-11具有协同抗结直肠癌的作用,为新型联合治疗结直肠癌提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liposomal Vardenafil and Linagliptin Combined with Irinotecan for Synergistic Colorectal Cancer Therapy.

Background: Irinotecan (CPT-11) is a standard first-line chemotherapy treatment for colorectal cancer (CRC). However, its clinical application is often comprised by gastrointestinal toxicity and limited therapeutic efficacy. Our previous study has revealed that the combination of Vardenafil (Vard) and Linagliptin (Linag) significantly alleviated CPT-11-induced intestinal toxicity in both in vitro and in vivo models. It remains unclear whether this combination can synergistically enhance the anticancer activity of CPT-11.

Methods: The in vitro synergism of Vard, Linag, and CPT-11 was assessed using cell viability assays on CRC cell lines, including HCT116, SW620, and HT29. An in vivo xenograft mouse model was established to evaluate the drug efficacy of both the original and liposomal forms of Vard and Linag combined with CPT-11. Additionally, untargeted metabolomics was utilized to explore the potential mechanisms underlying the observed synergistic effects.

Results: In vitro, the combination of Vard and Linag synergistically enhanced the anticancer activity of CPT-11 in CRC cell lines. In vivo, liposomal formulations of Vard and Linag tended to accumulate at the tumor site, improving drug targeting and synergistically enhancing the anticancer efficacy of CPT-11. Untargeted metabolomics analysis revealed that this synergistic effect was probably mediated through the regulation of lysophospholipid metabolism.

Conclusion: Liposomal Vard and Linag combined with CPT-11 demonstrated a synergistic anti-CRC effect, offering valuable insights into novel combination therapies in CRC treatment.

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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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