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基于纳米载体的小分子与siRNA/miRNA共递送用于癌症治疗

Nanocarrier-based co-delivery of small molecules and siRNA/miRNA for treatment of cancer.

作者信息

Chitkara Deepak, Singh Saurabh, Mittal Anupama

机构信息

Department of Pharmacy, Birla Institute of Technology & Science (BITS), Pilani Campus, Vidya Vihar, Pilani - 333 031 (Rajasthan), India.

Novartis Healthcare Pvt. Ltd, Hyderabad, Andhra Pradesh, India.

出版信息

Ther Deliv. 2016;7(4):245-55. doi: 10.4155/tde-2015-0003.

Abstract

Aberrant gene expression can trigger several vital molecular events that not only result in carcinogenesis but also cause chemoresistance, metastasis and relapse. Gene-based therapies using siRNA/miRNA have been suggested as new treatment method to improve the current regimen. Although these agents can restore the normal molecular cascade thereby resensitizing the cancer cells, delivering a standard regimen (either subsequently or simultaneously) is necessary to achieve the therapeutic benefit. However, co-delivery using a single carrier could give an additional advantage of similar biodistribution profile of the loaded agents. While much research has been carried out in this field in recent years, challenges involved in designing combination formulations including efficient coloading, stability, appropriate biodistribution and target specificity have hampered their clinical translation. This article highlights current aspects of nano-carriers used for co-delivery of small molecules and genes to treat cancer.

摘要

异常的基因表达可引发多种重要的分子事件,这些事件不仅会导致癌症发生,还会引起化疗耐药、转移和复发。使用小分子干扰RNA/微小RNA的基因疗法已被提议作为改善当前治疗方案的新治疗方法。尽管这些药物可以恢复正常的分子级联反应,从而使癌细胞重新敏感,但为了获得治疗益处,采用标准治疗方案(随后或同时)是必要的。然而,使用单一载体进行共递送可以使负载药物具有相似的生物分布特征,从而带来额外的优势。近年来,尽管该领域已经开展了大量研究,但设计联合制剂所涉及的挑战,包括高效共负载、稳定性、适当的生物分布和靶向特异性,阻碍了它们向临床转化。本文重点介绍了用于小分子和基因共递送以治疗癌症的纳米载体的当前研究情况。

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