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Nanocarrier mediated Delivery of siRNA/miRNA in Combination with Chemotherapeutic Agents for Cancer Therapy: Current Progress and Advances

机译:纳米载体介导的siRNA / miRNA与化疗药物联合用于癌症治疗的递送:当前的进展和进展

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摘要

Chemotherapeutic agents have certain limitations when it comes to treating cancer, the most important being severe side effects along with multidrug resistance developed against them. Tumor cells exhibits drug resistance due to activation of various cellular level processes viz. activation of drug efflux pumps, anti-apoptotic defense mechanisms etc. Currently, RNA interference (RNAi) based therapeutic approaches are under vibrant scrutinization to seek cancer cure. Especially small interfering RNA (siRNA) and micro RNA (miRNA), are able to knock down the carcinogenic genes by targeting the mRNA expression, which underlies the uniqueness of this therapeutic approach. Recent research focus in the regime of cancer therapy involves the engagement of targeted delivery of siRNA/miRNA in combinations with other therapeutic agents (such as gene, DNA or chemotherapeutic drug) for targeting permeability glycoprotein (P-gp), Multidrug resistant protein 1(MRP-1), B-cell lymphoma (BCL-2) and other targets that are mainly responsible for resistance in cancer therapy. RNAi-chemotherapeutic drug combinations have also been found to be effective against different molecular targets as well and can increase the sensitization of cancer cells to therapy several folds. However, due to stability issues associated with siRNA/miRNA suitable protective carrier is needed and nanotechnology based approaches have been widely explored to overcome these drawbacks. Furthermore, it has been univocally advocated that the co-delivery of siRNA/miRNA with other chemodrugs significantly enhances their capability to overcome cancer resistance compared to naked counterparts. The objective of this article is to review recent nanocarrier based approaches adopted for the delivery of siRNA/miRNA combinations with other anticancer agents (siRNA/miRNA/pDNA/chemodrugs) to treat cancer.
机译:化学治疗剂在治疗癌症方面有一定的局限性,最重要的是严重的副作用以及对它们产生的多药耐药性。肿瘤细胞由于各种细胞水平过程的激活而表现出耐药性。激活药物外排泵,抗凋亡防御机制等。目前,基于RNA干扰(RNAi)的治疗方法正在严格审查中,以寻求治愈癌症的方法。特别是小的干扰RNA(siRNA)和micro RNA(miRNA)能够通过靶向mRNA表达来敲除致癌基因,这奠定了这种治疗方法的独特性。近期针对癌症治疗方案的研究涉及将siRNA / miRNA与其他治疗药物(例如基因,DNA或化学治疗药物)联合靶向递送,以靶向通透性糖蛋白(P-gp),多药耐药蛋白1( MRP-1),B细胞淋巴瘤(BCL-2)和其他主要负责抗癌治疗的靶标。还已经发现,RNAi-化学疗法药物组合对于不同的分子靶标也有效,并且可以增加癌细胞对疗法的敏感性几倍。然而,由于与siRNA / miRNA相关的稳定性问题,需要合适的保护性载体,并且已经广泛探索了基于纳米技术的方法来克服这些缺点。此外,一直明确主张,与裸露的同类药物相比,siRNA / miRNA与其他化学药物的共同给药显着增强了它们克服癌症抵抗力的能力。本文的目的是回顾最近基于纳米载体的方法,该方法用于与其他抗癌药物(siRNA / miRNA / pDNA /化学药物)一起递送siRNA / miRNA组合。

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