Department of Biochemistry and Molecular Biology I, School of Biology, Complutense University, Madrid, Spain; Instituto de Investigaciones Sanitarias San Carlos (IdISSC), 28040 Madrid, Spain; Instituto Universitario de Investigación Neuroquímica, Complutense University, 28040 Madrid, Spain.
Department of Biochemistry and Molecular Biology I, School of Biology, Complutense University, Madrid, Spain.
Biochem Pharmacol. 2018 Nov;157:266-274. doi: 10.1016/j.bcp.2018.09.007. Epub 2018 Sep 7.
Glioblastoma multiforme (GBM) is the most frequent and aggressive type of brain tumor due, at least in part, to its poor response to current anticancer treatments. These features could be explained, at least partially, by the presence within the tumor mass of a small population of cells termed Glioma Initiating Cells (GICs) that has been proposed to be responsible for the relapses occurring in this disease. Thus, the development of novel therapeutic approaches (and specifically those targeting the population of GICs) is urgently needed to improve the survival of the patients suffering this devastating disease. Previous observations by our group and others have shown that Δ-Tetrahydrocannabinol (THC, the main active ingredient of marijuana) and other cannabinoids including cannabidiol (CBD) exert antitumoral actions in several animal models of cancer, including gliomas. We also found that the administration of THC (or of THC + CBD at a 1:1 ratio) in combination with temozolomide (TMZ), the benchmark agent for the treatment of GBM, synergistically reduces the growth of glioma xenografts. In this work we investigated the effect of the combination of TMZ and THC:CBD mixtures containing different ratios of the two cannabinoids in preclinical glioma models, including those derived from GICs. Our findings show that TMZ + THC:CBD combinations containing a higher proportion of CDB (but not TMZ + CBD alone) produce a similar antitumoral effect as the administration of TMZ together with THC and CBD at a 1:1 ratio in xenografts generated with glioma cell lines. In addition, we also found that the administration of TMZ + THC:CBD at a 1:1 ratio reduced the growth of orthotopic xenografts generated with GICs derived from GBM patients and enhanced the survival of the animals bearing these intracranial xenografts. Remarkably, the antitumoral effect observed in GICs-derived xenografts was stronger when TMZ was administered together with cannabinoid combinations containing a higher proportion of CBD. These findings support the notion that the administration of TMZ together with THC:CBD combinations - and specifically those containing a higher proportion of CBD - may be therapeutically explored to target the population of GICs in GBM.
多形性胶质母细胞瘤(GBM)是最常见和侵袭性最强的脑肿瘤类型,这至少部分归因于其对当前抗癌治疗的反应不佳。这些特征至少可以部分解释为肿瘤内存在一小部分细胞,称为胶质瘤起始细胞(GICs),据推测,这些细胞是导致该疾病复发的原因。因此,迫切需要开发新的治疗方法(特别是针对 GIC 群体的方法),以提高患有这种毁灭性疾病的患者的生存率。我们小组和其他小组之前的观察结果表明,Δ-四氢大麻酚(THC,大麻的主要活性成分)和其他大麻素,包括大麻二酚(CBD),在包括神经胶质瘤在内的几种癌症动物模型中发挥抗肿瘤作用。我们还发现,THC(或 THC+CBD 以 1:1 的比例)联合替莫唑胺(TMZ)(治疗 GBM 的基准药物)给药协同减少神经胶质瘤异种移植物的生长。在这项工作中,我们研究了 TMZ 与 THC:CBD 混合物组合在临床前神经胶质瘤模型中的作用,包括源自 GIC 的模型。我们的研究结果表明,TMZ+THC:CBD 混合物中含有较高比例 CBD 的组合(而不是 TMZ+CBD 单独)在与源自 GBM 患者的 GIC 生成的异种移植物中与 TMZ 联合 THC 和 CBD 以 1:1 的比例给药产生相似的抗肿瘤作用。此外,我们还发现 TMZ+THC:CBD 以 1:1 的比例给药可减少源自 GBM 患者的 GIC 衍生的原位异种移植物的生长,并提高携带这些颅内异种移植物的动物的存活率。值得注意的是,当 TMZ 与含有较高 CBD 比例的大麻素组合联合给药时,在源自 GIC 的异种移植物中观察到的抗肿瘤作用更强。这些发现支持这样的观点,即 TMZ 与 THC:CBD 组合联合给药 - 特别是那些含有较高 CBD 比例的组合 - 可能会被探索用于针对 GBM 中的 GIC 群体。