Division of Molecular Medicine, Bose Institute, P-1/12, CIT Scheme VII M, Kolkata-700 054, India.
Anticancer Res. 2012 Jul;32(7):2567-84.
Chemotherapy remains the core of anticancer treatment. However, despite the tremendous strides made in the development of targeted anticancer therapies, emergence of resistance to chemotherapeutic drugs is still a major obstacle in the successful management of resistant tumours. Therefore, profound investigation into the in-depth molecular mechanisms of drug resistance is essential and may hopefully translate into effective therapies that can flip the switch from drug resistance to susceptibility. Mechanistically, resistance phenomena may be explained by (i) overexpression of drug efflux pumps, (ii) enhanced drug detoxification, (iii) rapid DNA repair efficiency, (iv) defects in apoptosis regulation, and (v) active cell survival signals. Several adverse effects associated with multidrug resistance and the need for safe multi-targeted anticancer drugs instigated the use of the phytochemical, curcumin, the yellow pigment of the spice turmeric, which has pleotropic activities. We performed a structured literature review using PubMed and Medline searches with secondary review of cited publications, identifying studies on the role of curcumin in conquering drug resistance in cancer. This review describes how curcumin sensitizes cancer cells through regulation of multiple multidrug resistance pathways, thus employing one drug for multiple targets. Curcumin helps the cancer cells to regain their 'forgotten' apoptosis, modulates drug-target interaction at different levels, restrains survival pathways when their proteins are overexpressed, and finds an alternate way to carry forward the process of sensitization of different resistant tumours. Additionally, the review dissects the role of curcumin, if any, in targeting the major culprit of drug resistance, cancer stem cells (CSC), thereby circumventing resistance. Taken together, this review strongly suggests that curcumin is a promising chemosensitizing agent and that the unique properties of curcumin may be exploited for successful management of resistant tumours.
化疗仍然是抗癌治疗的核心。然而,尽管在开发针对癌症的靶向治疗方面取得了巨大进展,但对化疗药物的耐药性仍然是成功治疗耐药肿瘤的主要障碍。因此,深入研究耐药性的深层次分子机制至关重要,并有望转化为有效的治疗方法,使耐药性转变为敏感性。从机制上讲,耐药现象可以用以下几种方式来解释:(i)药物外排泵的过度表达,(ii)增强的药物解毒作用,(iii)快速的 DNA 修复效率,(iv)细胞凋亡调控缺陷,和(v)活跃的细胞存活信号。与多药耐药性相关的几种不良反应以及对安全的多靶点抗癌药物的需求促使人们使用植物化学物质姜黄素,它是姜黄的黄色色素,具有多种作用。我们使用 PubMed 和 Medline 进行了结构化文献综述,并对引用文献进行了二次审查,以确定关于姜黄素在克服癌症耐药性方面作用的研究。本综述描述了姜黄素如何通过调节多种多药耐药途径使癌细胞变得敏感,从而使一种药物针对多个靶点。姜黄素帮助癌细胞重新获得“遗忘”的细胞凋亡,在不同水平调节药物-靶标相互作用,当它们的蛋白质过度表达时抑制存活途径,并找到一种替代方法来推进不同耐药肿瘤的敏化过程。此外,该综述还分析了姜黄素在靶向耐药性的主要罪魁祸首——癌症干细胞(CSC)方面的作用,如果有的话,从而规避耐药性。综上所述,本综述强烈表明姜黄素是一种很有前途的化疗增敏剂,并且姜黄素的独特特性可能被用于成功治疗耐药肿瘤。