香豆素A的抗癌特性及其与吉西他滨、顺铂和大麻素在膀胱癌中的潜在协同作用。

Andrea M Tomko, Erin G Whynot, Denis J Dupré
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引用次数: 12

摘要

几项研究表明,大麻中存在的成分在不同的模型中具有抗肿瘤作用。不幸的是,人们对大麻中存在的大多数化合物在膀胱癌中的潜在抗肿瘤作用以及这些化合物如何潜在地积极或消极地影响化疗药物的作用知之甚少。我们的研究旨在评估大麻中发现的一种化合物的作用,这种化合物至今尚未得到广泛的研究,即香豆素a,在膀胱癌细胞系中的作用。我们的目的是确定canflavin A与常用治疗膀胱癌的药物(如吉西他滨和顺铂)联合治疗是否能够产生协同效应。我们还评估了大麻素A与各种大麻素的共同治疗是否能产生协同效应。方法:采用两种移行细胞癌细胞系,观察100 μM的黄酮类cannflavin A的细胞毒作用。我们测试了cannflavin A与吉西他滨(达100 nM)、顺铂(达100 μM)和大麻素(达10 μM)的潜在协同细胞毒作用。我们还使用膜联蛋白V评估了凋亡级联的激活,并使用Matrigel试验评估了cannflavin A是否具有减少侵袭的能力。结果:在对cannflavin a的反应中,膀胱癌细胞系的细胞活力以浓度依赖性的方式受到影响,并且其与吉西他滨或顺铂的联合诱导了从拮抗到辅助的不同反应,在某些情况下也观察到协同作用,这取决于所使用的浓度和药物。Cannflavin A还通过caspase 3裂解激活细胞凋亡,并能减少50%的侵袭。有趣的是,在膀胱癌细胞系中,大麻素A与其他大麻素如Δ9-tetrahydrocannabinol、大麻二酚、大麻色胺和大麻素表现出协同作用。讨论:我们的研究结果表明,大麻中除大麻素外的化合物,如类黄酮cannflavin A,对人类膀胱移行癌细胞具有细胞毒性,并且该化合物与其他药物联合使用时可以发挥协同作用。在体内的研究将需要确认鱼头黄素A作为一种潜在的药物膀胱癌治疗的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-cancer properties of cannflavin A and potential synergistic effects with gemcitabine, cisplatin, and cannabinoids in bladder cancer.

Anti-cancer properties of cannflavin A and potential synergistic effects with gemcitabine, cisplatin, and cannabinoids in bladder cancer.

Anti-cancer properties of cannflavin A and potential synergistic effects with gemcitabine, cisplatin, and cannabinoids in bladder cancer.

Anti-cancer properties of cannflavin A and potential synergistic effects with gemcitabine, cisplatin, and cannabinoids in bladder cancer.

Introduction: Several studies have shown anti-tumor effects of components present in cannabis in different models. Unfortunately, little is known about the potential anti-tumoral effects of most compounds present in cannabis in bladder cancer and how these compounds could potentially positively or negatively impact the actions of chemotherapeutic agents. Our study aims to evaluate the effects of a compound found in Cannabis sativa that has not been extensively studied to date, cannflavin A, in bladder cancer cell lines. We aimed to identify whether cannflavin A co-treatment with agents commonly used to treat bladder cancer, such as gemcitabine and cisplatin, is able to produce synergistic effects. We also evaluated whether co-treatment of cannflavin A with various cannabinoids could produce synergistic effects.

Methods: Two transitional cell carcinoma cell lines were used to assess the cytotoxic effects of the flavonoid cannflavin A up to 100 μM. We tested the potential synergistic cytotoxic effects of cannflavin A with gemcitabine (up to 100 nM), cisplatin (up to 100 μM), and cannabinoids (up to 10 μM). We also evaluated the activation of the apoptotic cascade using annexin V and whether cannflavin A has the ability to reduce invasion using a Matrigel assay.

Results: Cell viability of bladder cancer cell lines was affected in a concentration-dependent fashion in response to cannflavin A, and its combination with gemcitabine or cisplatin induced differential responses-from antagonistic to additive-and synergism was also observed in some instances, depending on the concentrations and drugs used. Cannflavin A also activated apoptosis via caspase 3 cleavage and was able to reduce invasion by 50%. Interestingly, cannflavin A displayed synergistic properties with other cannabinoids like Δ9-tetrahydrocannabinol, cannabidiol, cannabichromene, and cannabivarin in the bladder cancer cell lines.

Discussion: Our results indicate that compounds from Cannabis sativa other than cannabinoids, like the flavonoid cannflavin A, can be cytotoxic to human bladder transitional carcinoma cells and that this compound can exert synergistic effects when combined with other agents. In vivo studies will be needed to confirm the activity of cannflavin A as a potential agent for bladder cancer treatment.

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