Literature DB >> 28363142

Local co-administration of gene-silencing RNA and drugs in cancer therapy: State-of-the art and therapeutic potential.

Mikael Larsson1, Wei-Ting Huang2, Dean-Mo Liu2, Dusan Losic3.   

Abstract

Gene-silencing miRNA and siRNA are emerging as attractive therapeutics with potential to suppress any genes, which could be especially useful in combination cancer therapy to overcome multidrug resistant (MDR) cancer. Nanomedicine aims to advance cancer treatment through functional nanocarriers that delivers one or more therapeutics to cancer tissue and cells with minimal off-target effects and suitable release kinetics and dosages. Although much effort has gone into developing circulating nanocarriers with targeting functionality for systemic administration, another alternative and straightforward approach is to utilize formulations to be administered directly to the site of action, such as pulmonary and intratumoral delivery. The combination of gene-silencing RNA with drugs in nanocarriers for localized delivery is emerging with promising results. In this review, the current progress and strategies for local co-administration of RNA and drug for synergistic effects and future potential in cancer treatment are presented and discussed. Key advances in RNA-drug anticancer synergy and localized delivery systems were combined with a review of the available literature on local co-administration of RNA and drug for cancer treatment. It is concluded that advanced delivery systems for local administration of gene-silencing RNA and drug hold potential in treatment of cancer, depending on indication. In particular, there are promising developments using pulmonary delivery and intratumoral delivery in murine models, but further research should be conducted on other local administration strategies, designs that achieve effective intracellular delivery and maximize synergy and feasibility for clinical use.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Combinatory treatment; Drug delivery system; RNA; Synergy; Therapeutic substance; Tumor

Mesh:

Substances:

Year:  2017        PMID: 28363142     DOI: 10.1016/j.ctrv.2017.03.004

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  6 in total

Review 1.  Current Trends and Challenges in the Clinical Translation of Nanoparticulate Nanomedicines: Pathways for Translational Development and Commercialization.

Authors:  Susan Hua; Maria B C de Matos; Josbert M Metselaar; Gert Storm
Journal:  Front Pharmacol       Date:  2018-07-17       Impact factor: 5.810

2.  Local delivery of arsenic trioxide nanoparticles for hepatocellular carcinoma treatment.

Authors:  Jian Hu; Yi Dong; Li Ding; Yang Dong; Zhihua Wu; Wenping Wang; Ming Shen; Yourong Duan
Journal:  Signal Transduct Target Ther       Date:  2019-09-06

3.  Dendriplex-Impregnated Hydrogels With Programmed Release Rate.

Authors:  Evgeny Apartsin; Alya Venyaminova; Jean-Pierre Majoral; Anne-Marie Caminade
Journal:  Front Chem       Date:  2022-01-05       Impact factor: 5.221

Review 4.  The Current Status of SSRP1 in Cancer: Tribulation and Road Ahead.

Authors:  Shengnan Jia; Baofeng Guo; Lihui Wang; Liping Peng; Ling Zhang
Journal:  J Healthc Eng       Date:  2022-04-13       Impact factor: 3.822

Review 5.  Biocompatible Iron Oxide Nanoparticles for Targeted Cancer Gene Therapy: A Review.

Authors:  Jinsong Zhang; Tianyuan Zhang; Jianqing Gao
Journal:  Nanomaterials (Basel)       Date:  2022-09-24       Impact factor: 5.719

Review 6.  Drug Delivery Nanosystems for the Localized Treatment of Glioblastoma Multiforme.

Authors:  L Nam; C Coll; L C S Erthal; C de la Torre; D Serrano; R Martínez-Máñez; M J Santos-Martínez; E Ruiz-Hernández
Journal:  Materials (Basel)       Date:  2018-05-11       Impact factor: 3.623

  6 in total

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