Cannabinoids as Potential Cancer Therapeutics: The Concentration Conundrum.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Cannabis and Cannabinoid Research Pub Date : 2024-08-01 Epub Date: 2023-03-21 DOI:10.1089/can.2022.0344
Nurgul Carkaci-Salli, Wesley M Raup-Konsavage, Deepkamal Karelia, Dongxiao Sun, Cheng Jiang, Junxuan Lu, Kent E Vrana
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引用次数: 0

Abstract

Background: Studies have reported that cannabinoids, in particular Δ9-tetrahydrocannabinol (Δ9-THC) and cannabidiol (CBD), significantly reduce cancer cell viability in vitro. Unfortunately, treatment conditions vary significantly across reports. In particular, a majority of reports utilize conditions with reduced serum concentrations (0-3%) that may compromise the growth of the cells themselves, as well as the observed results. Objectives: This study was designed to test the hypothesis that, based on their known protein binding characteristics, cannabinoids would be less effective in the presence of fetal bovine serum (FBS). Moreover, we wished to determine if the treatments served to be cytotoxic or cytostatic under these conditions. Methods: Six cancer cell lines, representing two independent lines of three different types of cancer (glioblastoma, melanoma, and colorectal cancer [CRC]), were treated with 10 μM pure Δ9-THC, CBD, KM-233, and HU-331 for 48 h (in the presence or absence of FBS). Cell viability was measured with the MTT assay. Dose-response curves were then generated comparing the potencies of the four cannabinoids under the same conditions. Results: We found that serum-free medium alone produces cell cycle arrest for CRC cells and slows cell growth for the other cancer types. The antineoplastic effects of three of the four cannabinoids (Δ9-THC, CBD, and KM-233) increase when serum is omitted from the media. In addition, dose-response curves for these drugs demonstrated lower IC50 values for serum-free media compared with the media with 10% serum in all cell lines. The fourth compound, HU-331, was equally effective under both conditions. A further confound we observed is that omission of serum produces dramatic binding of Δ9-THC and CBD to plastic. Conclusions: Treatment of cancer cells in the absence of FBS appears to enhance the potency of cannabinoids. However, omission of FBS itself compromises cell growth and represents a less physiological condition. Given the knowledge that cannabinoids are 90-95% protein bound and have well-known affinities for plastic, it may be ill-advised to treat cells under conditions where the cells are not growing optimally and where known concentrations cannot be assumed (i.e., FBS-free conditions).

大麻素作为潜在的癌症治疗药物:浓度难题。
背景:有研究报告称,大麻素,尤其是Δ9-四氢大麻酚(Δ9-THC)和大麻二酚(CBD),可显著降低体外癌细胞的存活率。遗憾的是,不同报告的治疗条件差异很大。特别是,大多数报告都使用了血清浓度较低(0-3%)的条件,这可能会影响细胞本身的生长以及观察到的结果。研究目的本研究旨在验证一个假设,即根据已知的蛋白质结合特性,大麻素在有胎牛血清(FBS)存在的情况下效果较差。此外,我们还希望确定在这些条件下治疗是否具有细胞毒性或细胞抑制作用。研究方法代表三种不同类型癌症(胶质母细胞瘤、黑色素瘤和结肠直肠癌 [CRC])的两个独立品系的六种癌细胞株分别用 10 μM 纯 Δ9-THC、CBD、KM-233 和 HU-331 处理 48 小时(有无 FBS 均可)。细胞活力用 MTT 法检测。然后生成剂量反应曲线,比较四种大麻素在相同条件下的效力。结果:我们发现,仅无血清培养基就能使 CRC 细胞的细胞周期停止,并减缓其他癌症类型的细胞生长。四种大麻素中的三种(Δ9-THC、CBD 和 KM-233)的抗肿瘤作用在培养基中不添加血清时会增强。此外,这些药物的剂量反应曲线显示,在所有细胞系中,无血清培养基的 IC50 值低于含 10%血清的培养基。第四种化合物 HU-331 在这两种条件下同样有效。我们观察到的另一个干扰因素是,不加血清会使Δ9-THC 和 CBD 与塑料发生剧烈结合。结论在无 FBS 的情况下处理癌细胞似乎能增强大麻素的效力。然而,不添加 FBS 本身就会影响细胞生长,并代表一种较低的生理状态。鉴于大麻素 90-95% 与蛋白质结合,并且与塑料具有众所周知的亲和力,在细胞生长不理想和无法假定已知浓度的条件下(即无 FBS 条件下)处理细胞可能是不明智的。
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来源期刊
Cannabis and Cannabinoid Research
Cannabis and Cannabinoid Research PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
7.90%
发文量
164
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