1. Academic Validation
  2. Salinomycin-Loaded Small-Molecule Nanoprodrugs Enhance Anticancer Activity in Hepatocellular Carcinoma

Salinomycin-Loaded Small-Molecule Nanoprodrugs Enhance Anticancer Activity in Hepatocellular Carcinoma

  • Int J Nanomedicine. 2020 Sep 15;15:6839-6854. doi: 10.2147/IJN.S236928.
Jianguo Wang  # 1 Jianyong Zhuo  # 2 Yaoye Tao 2 Shengjun Xu 2 Zun Chen 2 Fan Yang 2 Qinghong Ke 2 3 Haiyang Xie 2 3 Shusen Zheng 2 3 4 Hangxiang Wang 2 3 Xiao Xu 1
Affiliations

Affiliations

  • 1 Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People's Republic of China.
  • 2 NHC Key Laboratory of Combined Multi-Organ Transplantation, Hangzhou 310003, People's Republic of China.
  • 3 Department of Hepatobiliary and Pancreatic Surgery, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, People's Republic of China.
  • 4 Department of Hepatobiliary and Pancreatic Surgery, Shulan (Hangzhou) Hospital, Hangzhou 310003, People's Republic of China.
  • # Contributed equally.
Abstract

Background: There is currently no effective treatment for advanced hepatocellular carcinoma (HCC), and chemotherapy has little effect on long-term survival of HCC patients, largely due to the Cancer stem cell (CSC) chemoresistance of HCC.

Methods: We constructed a small-molecule nanometer-sized prodrug (nanoprodrug) loaded with salinomycin (SAL) for the treatment of HCC. SAL was encapsulated by the prodrug LA-SN38 (linoleic acid modified 7-ethyl-10-hydroxycamptothecin) to construct a self-assembled nanoprodrug further PEGylated with DSPE-PEG2000. We characterized this codelivered nanoprodrug and its antitumor activity both in vitro in human HCC cell lines and in vivo in mice.

Results: Delivery of the SAL- and LA-SN38-based nanoprodrugs effectively promoted Apoptosis of HCC cells, exerted inhibition of HCC tumor-sphere formation as well as HCC cell motility and invasion, and reduced the proportion of CD133+ HCC-CSC cells. In nude mice, the nanoprodrug suppressed growth of tumor xenografts derived from human cell lines and patient.

Conclusion: Our results show that SAL-based nanoprodrugs are a promising platform for treating patients with HCC and a novel strategy for combination therapy of cancers.

Keywords

cancer stem cells; hepatocellular carcinoma; salinomycin; self-assemble; small-molecule prodrugs.

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