Paulista School of Medicine, Federal University of São Paulo, Av. Ascendino Reis, 763, Vila Clementino, São Paulo, SP, 04027-000, Brazil,
J Neurooncol. 2014 Jan;116(1):11-24. doi: 10.1007/s11060-013-1277-1. Epub 2013 Oct 20.
To evaluate, through a systematic review of the literature, the antitumoral effects of cannabinoids on gliomas. Research included the following electronic databases: PUBMED, EMBASE, LILACS and The Cochrane Collaboration Controlled Trials Register. All published studies involving the antitumoral effects (cellular and molecular mechanisms) of cannabinoids were considered for this review. The bibliography search strategy included all publications of each of these databases until December 31, 2012. From 2,260 initially identified articles, 35 fulfilled the inclusion criteria for this review. All the studies included in this systematic review were experimental (in vivo and/or in vitro), except for one pilot clinical trial phase I/II involving humans. In all experimental studies included, cannabinoids exerted antitumoral activity in vitro and/or antitumoral evidence in vivo in several models of tumor cells and tumors. The antitumor activity included: antiproliferative effects (cell cycle arrest), decreased viability and cell death by toxicity, apoptosis, necrosis, autophagy, as well as antiangiogenic and antimigratory effects. Antitumoral evidence included: reduction in tumor size, antiangiogenic, and antimetastatic effects. Additionally, most of the studies described that the canabinnoids exercised selective antitumoral action in several distinct tumor models. Thereby, normal cells used as controls were not affected. The safety factor in the cannabinoids' administration has also been demonstrated in vivo. The various cannabinoids tested in multiple tumor models showed antitumoral effects both in vitro and in vivo. These findings indicate that cannabinoids are promising compounds for the treatment of gliomas.
为了评估大麻素类药物对神经胶质瘤的抗肿瘤作用,我们对文献进行了系统评价。研究包括以下电子数据库:PUBMED、EMBASE、LILACS 和 Cochrane 协作临床试验注册中心。所有涉及大麻素类药物抗肿瘤作用(细胞和分子机制)的已发表研究均被纳入本综述。文献检索策略包括每个数据库的所有出版物,检索时间截至 2012 年 12 月 31 日。从最初确定的 2260 篇文章中,有 35 篇符合本综述的纳入标准。本系统评价纳入的所有研究均为实验性研究(体内和/或体外),除了一项涉及人类的 I/II 期临床试验。在所有纳入的实验研究中,大麻素类药物在体外均具有抗肿瘤活性,在几种肿瘤细胞和肿瘤的体内模型中均具有抗肿瘤证据。抗肿瘤活性包括:增殖抑制作用(细胞周期停滞)、毒性降低细胞活力和细胞死亡、细胞凋亡、细胞坏死、自噬以及抗血管生成和抗迁移作用。抗肿瘤证据包括:肿瘤体积缩小、抗血管生成和抗转移作用。此外,大多数研究表明,大麻素类药物在几种不同的肿瘤模型中具有选择性抗肿瘤作用。作为对照的正常细胞未受影响。大麻素类药物在体内的安全性因素也得到了证明。多种大麻素类药物在多种肿瘤模型中的测试均显示出体外和体内的抗肿瘤作用。这些发现表明大麻素类药物是治疗神经胶质瘤的有前途的化合物。