Issue 4, 2016

Polymer nanoparticle delivery of dichloroacetate and DACH-Pt to enhance antitumor efficacy and lower systemic toxicity

Abstract

Platinum agents can cause DNA damage and thus induce apoptosis of cancer cells, which has made them the backbone of cancer chemotherapy regimens. However, most cancers will develop drug resistance over the course of treatment. Meanwhile, most tumors meet energy needs largely by aerobic glycolysis (glycolysis in the presence of oxygen, called the Warburg effect), which is related to their resistance to apoptosis. Therefore, we have used a biodegradable polymer carrier to conjugate with DACH-Pt and dichloroacetate, a PDK inhibitor that can reverse the Warburg effect and derepress the resistance to apoptosis, thus sensitizing cancer cells to platinum. The as-prepared polymer–drug conjugates can be assembled into nanoparticles for effective delivery and better synergism. In vitro and in vivo studies revealed that the combination of polymer–DCA and polymer–DACH-Pt are much better than the free drugs administered simultaneously, in terms of both safety and antitumor efficacy.

Graphical abstract: Polymer nanoparticle delivery of dichloroacetate and DACH-Pt to enhance antitumor efficacy and lower systemic toxicity

Article information

Article type
Paper
Submitted
08 Oct 2015
Accepted
11 Jan 2016
First published
26 Jan 2016

Biomater. Sci., 2016,4, 661-669

Author version available

Polymer nanoparticle delivery of dichloroacetate and DACH-Pt to enhance antitumor efficacy and lower systemic toxicity

Q. Yang, J. Cai, S. Sun, X. Kang, J. Guo, Y. Zhu, L. Yan, X. Jing and Z. Wang, Biomater. Sci., 2016, 4, 661 DOI: 10.1039/C5BM00439J

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