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Review Article

Combinatorial therapeutic approaches with RNAi and anticancer drugs using nanodrug delivery systems

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Pages 1391-1401 | Received 11 Nov 2016, Accepted 23 Mar 2017, Published online: 19 May 2017

Figures & data

Figure 1. Illustration depicts multidrug resistance (MDR) mechanisms in cancer cells. Enhanced drug efflux, expression of MDR proteins, reduced drug uptake, poor drug target interaction and deregulated apoptosis are some of the important mechanisms.

Figure 1. Illustration depicts multidrug resistance (MDR) mechanisms in cancer cells. Enhanced drug efflux, expression of MDR proteins, reduced drug uptake, poor drug target interaction and deregulated apoptosis are some of the important mechanisms.

Figure 2. Nanoparticle-based co-delivery of siRNA and chemotherapeutic drug overcomes MDR by siRNA-mediated p-glycoprotein (p-gp) suppression. Increased drug accumulation in cells triggers apoptosis mechanisms.

Figure 2. Nanoparticle-based co-delivery of siRNA and chemotherapeutic drug overcomes MDR by siRNA-mediated p-glycoprotein (p-gp) suppression. Increased drug accumulation in cells triggers apoptosis mechanisms.

Table 1. Co-delivery of miRNA, miRNA inhibitor or plasmid DNA with other cancer therapeutic agents via nanoparticles.