大麻二酚和Δ9-tetrahydrocannabinol的抗癌特性及其与吉西他滨和顺铂在膀胱癌细胞系中的协同作用。

Erin G Whynot, Andrea M Tomko, Denis J Dupré
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引用次数: 4

摘要

导言:随着世界上多个司法管辖区的大麻合法化,越来越多的人口消费大麻。几项研究表明,在不同的模型中,大麻中存在的成分具有抗肿瘤作用。不幸的是,人们对大麻素在膀胱癌中的潜在抗肿瘤作用以及大麻素如何与化疗药物协同作用知之甚少。我们的研究旨在确定大麻素(如大麻二酚和Δ9-tetrahydrocannabinol)与常用治疗膀胱癌的药物(如吉西他滨和顺铂)联合使用是否能产生理想的协同效应。我们还评估了不同大麻素的联合治疗是否会产生协同效应。方法:用几种药物,包括几种大麻素,制作浓度曲线,确定其对膀胱癌细胞株的抗肿瘤作用范围。我们测试了吉西他滨(≤100 nM)、顺铂(≤100 μM)和大麻素(≤10 μM)对T24和TCCSUP细胞的细胞毒性作用。我们还评估了凋亡级联的激活以及大麻素是否具有减少T24细胞侵袭的能力。结果:大麻二酚、Δ9-tetrahydrocannabinol、大麻色胺和大麻素降低膀胱癌细胞系的细胞活力,它们与吉西他滨或顺铂联合使用可能会引起不同的反应,从拮抗到添加和协同作用,这取决于所使用的浓度。在Matrigel实验中,大麻二酚和Δ9-tetrahydrocannabinol也显示通过caspase-3切割诱导细胞凋亡并减少侵袭。虽然单个大麻素可能足以降低膀胱癌细胞系的细胞活力,但大麻二酚和Δ9-tetrahydrocannabinol也显示出与其他大麻素(如大麻色胺或大麻素)的协同特性。讨论:我们的研究结果表明大麻素可以降低人膀胱移行细胞癌细胞的活力,并且当与其他药物联合使用时,它们可能会发挥协同作用。我们的体外研究结果将为未来的体内研究和临床试验奠定基础,以开发新的治疗方法,这可能对未来的膀胱癌治疗有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anticancer properties of cannabidiol and Δ<sup>9</sup>-tetrahydrocannabinol and synergistic effects with gemcitabine and cisplatin in bladder cancer cell lines.

Anticancer properties of cannabidiol and Δ<sup>9</sup>-tetrahydrocannabinol and synergistic effects with gemcitabine and cisplatin in bladder cancer cell lines.

Anticancer properties of cannabidiol and Δ<sup>9</sup>-tetrahydrocannabinol and synergistic effects with gemcitabine and cisplatin in bladder cancer cell lines.

Anticancer properties of cannabidiol and Δ9-tetrahydrocannabinol and synergistic effects with gemcitabine and cisplatin in bladder cancer cell lines.

Introduction: With the legalization of cannabis in multiple jurisdictions throughout the world, a larger proportion of the population consumes cannabis. Several studies have demonstrated anti-tumor effects of components present in cannabis in different models. Unfortunately, little is known about the potential anti-tumoral effects of cannabinoids in bladder cancer and how cannabinoids could potentially synergize with chemotherapeutic agents. Our study aims to identify whether a combination of cannabinoids, like cannabidiol and Δ9-tetrahydrocannabinol, with agents commonly used to treat bladder cancer, such as gemcitabine and cisplatin, can produce desirable synergistic effects. We also evaluated if co-treatment with different cannabinoids resulted in synergistic effects.

Methods: We generated concentration curves with several drugs, including several cannabinoids, to identify the range at which they could exert anti-tumor effects in bladder cancer cell lines. We tested the cytotoxic effects of gemcitabine (up to 100 nM), cisplatin (up to 100 μM), and cannabinoids (up to 10 μM) in T24 and TCCSUP cells. We also evaluated the activation of the apoptotic cascade and whether cannabinoids have the ability to reduce invasion in T24 cells.

Results: Cannabidiol, Δ9-tetrahydrocannabinol, cannabichromene, and cannabivarin reduce cell viability of bladder cancer cell lines, and their combination with gemcitabine or cisplatin may induce differential responses, from antagonistic to additive and synergistic effects, depending on the concentrations used. Cannabidiol and Δ9-tetrahydrocannabinol were also shown to induce apoptosis via caspase-3 cleavage and reduce invasion in a Matrigel assay. Cannabidiol and Δ9-tetrahydrocannabinol also display synergistic properties with other cannabinoids like cannabichromene or cannabivarin, although individual cannabinoids may be sufficient to reduce cell viability of bladder cancer cell lines.

Discussion: Our results indicate that cannabinoids can reduce human bladder transitional cell carcinoma cell viability, and that they can potentially exert synergistic effects when combined with other agents. Our in vitro results will form the basis for future studies in vivo and in clinical trials for the development of new therapies that could be beneficial for the treatment of bladder cancer in the future.

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