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Issue 4, 2019
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Flower-like gold nanoparticles for enhanced photothermal anticancer therapy by the delivery of pooled siRNA to inhibit heat shock stress response

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Abstract

Due to the anti-apoptotic effect employed by cells to protect themselves, recent research shows that photothermal therapy (PTT) can lead to heat shock response, thus reducing the effect of treatment on cancer cells. Small interfering RNA (siRNA), as an effective carrier of RNA interference, can silence the expression of heat shock protein, HSPs or BAG3 genes by inhibiting the expression of specific genes, and thereby inhibiting heat shock response and making cancer cells more sensitive to PTT. In this study, flower-like gold nanoparticles were used as a core for a layer-by-layer strategy to produce a safe and biodegradable nanoparticle platform for gene silencing and photothermal therapy. The results showed that when the mass ratio of the GNFs and siRNA was 20 : 1, the loading efficiency was above 90%, which can effectively silence the expression of BAG3 siRNA. We demonstrated that the GNFs–siRNA still had a good photothermal effect after siRNA modification. In vitro, the GNFs–siRNA showed good biocompatibility and effectively tumor killing properties after laser irradiation. Furthermore, the GNFs–siRNA with laser treatment significantly decreased the expression of BAG3 and remarkably inhibited tumor growth in vivo. This nanosystem establishes an optimized platform for future gene delivery and photothermal therapy.

Graphical abstract: Flower-like gold nanoparticles for enhanced photothermal anticancer therapy by the delivery of pooled siRNA to inhibit heat shock stress response

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Publication details

The article was received on 12 Sep 2018, accepted on 05 Dec 2018 and first published on 14 Dec 2018


Article type: Paper
DOI: 10.1039/C8TB02418A
Citation: J. Mater. Chem. B, 2019,7, 586-597

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    Flower-like gold nanoparticles for enhanced photothermal anticancer therapy by the delivery of pooled siRNA to inhibit heat shock stress response

    Y. Liu, M. Xu, Y. Zhao, X. Chen, X. Zhu, C. Wei, S. Zhao, J. Liu and X. Qin, J. Mater. Chem. B, 2019, 7, 586
    DOI: 10.1039/C8TB02418A

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