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Multi-Targeted Agents in Cancer Cell Chemosensitization: What We Learnt from Curcumin Thus Far

机译:癌细胞化学增敏中的多靶点药物:到目前为止我们从姜黄素中学到的东西

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Background: Research over the past several years has developed many mono-targeted therapies for the prevention and treatment of cancer, but it still remains one of the fatal diseases in the world killing 8.2 million people annually. It has been well-established that development of chemoresistance in cancer cells against mono-targeted chemotherapeutic agents by modulation of multiple survival pathways is the major cause of failure of cancer chemotherapy. Therefore, inhibition of these pathways by non-toxic multi-targeted agents may have profoundly high potential in preventing drug resistance and sensitizing cancer cells to chemotherapeutic agents. Objective: To study the potential of curcumin, a multi-targeted natural compound, obtained from the plant Turmeric (Curcuma longa) in combination with standard chemotherapeutic agents to inhibit drug resistance and sensitize cancer cells to these agents based on available literature and patents. Method: An extensive literature survey was performed in PubMed and Google for the chemosensitizing potential of curcumin in different cancers published so far and the patents published during 2014-2015. Result: Our search resulted in many in vitro, in vivo and clinical reports signifying the chemosensitizing potential of curcumin in diverse cancers. There were 160 in vitro studies, 62 in vivo studies and 5 clinical studies. Moreover, 11 studies reported on hybrid curcumin: the next generation of curcumin based therapeutics. Also, 34 patents on curcumin's biological activity have been retrieved. Conclusion: Altogether, the present study reveals the enormous potential of curcumin, a natural, non-toxic, multi-targeted agent in overcoming drug resistance in cancer cells and sensitizing them to chemotherapeutic drugs.
机译:背景:过去几年的研究已经开发出许多用于癌症预防和治疗的单靶标疗法,但它仍然是世界上每年致命的疾病之一,造成820万人死亡。众所周知,通过调节多种存活途径,癌细胞中针对单靶向化疗药物的化学耐药性的发展是癌症化疗失败的主要原因。因此,用无毒的多靶点药物抑制这些途径在预防耐药性和使癌细胞对化学治疗剂敏感方面具有巨大的潜力。目的:基于现有文献和专利,研究姜黄素(一种姜黄素)(一种多靶点天然化合物)与植物黄姜(Curcuma longa)以及标准化学治疗剂联合使用的潜力,可抑制其耐药性并使癌细胞对这些药物敏感。方法:在PubMed和Google上进行了广泛的文献调查,以了解姜黄素在迄今出版的不同癌症中以及2014-2015年期间公布的专利中对化学敏感性的潜力。结果:我们的搜索结果产生了许多体外,体内和临床报告,这些数据表明姜黄素在多种癌症中的化学增敏潜力。有160项体外研究,62项体内研究和5项临床研究。此外,有11项研究报道了混合姜黄素:下一代基于姜黄素的疗法。此外,已获得34项姜黄素生物活性专利。结论:总的来说,本研究揭示了姜黄素(一种天然,无毒,多靶点的药物)在克服癌细胞的耐药性并使它们对化疗药物敏感方面的巨大潜力。

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