Citation

  • Authors: Jilek, J. L., Zhang, Q. Y., Tu, M. J., Ho, P. Y., Duan, Z., Qiu, J. X., Yu, A. M.
  • Year: 2019
  • Journal: Mol Ther Nucleic Acids 14 498-508
  • Applications: in vivo / siRNA / in vivo-jetPEI

Method

One week post-inoculation, mice were assigned into five groups (untreated, lPEI/MSA, LPP/MSA, lPEI/let-7c, and LPP/let-7c) according to tumor sizes determined by in vivo bioluminescence imaging, and treated i.v. (40 µg RNA) three times per week through tail vein injection. Mice were imaged once per week to monitor tumor growth. Mice were sacrificed 2 h after the last dose on day 15. Livers with engrafted tumors were harvested and imaged for GFP fluorescence using ChemiDoc MP Imaging System.

Abstract

Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related deaths, warranting better therapies. Restoration of tumor-suppressive microRNAs depleted in hepatocellular carcinoma represents a new therapeutic strategy. Herein, we sought to identify a potent microRNA (miRNA) agent that could alleviate HCC tumor burden and improve survival. Among a collection of bioengineered noncoding RNA molecules produced through bacterial fermentation, we identified let-7c agent as the most potent inhibitor of HCC cell viability. Bioengineered let-7c selectively modulated target gene expression (Lin-28 homolog B [LIN28B], AT-rich interactive domain-containing protein 3B [ARID3B], B cell lymphoma-extra large [Bcl-xl], and c-Myc) in HCC cells, and consequently induced apoptosis and inhibited tumorsphere growth. When formulated with liposomal-branched polyethylenimine polyplex, bioengineered let-7c exhibited serum stability up to 24 h. Furthermore, liposomal polyplex-formulated let-7c could effectively reduce tumor burden and progression in orthotopic HCC mouse models, while linear polyethyleneimine-formulated let-7c to a lower degree, as revealed by live animal and ex vivo tissue imaging studies. This was also supported by reduced serum alpha-fetoprotein and bilirubin levels in let-7c-treated mice. In addition, lipopolyplex-formulated let-7c extended overall survival of HCC tumor-bearing mice and elicited no or minimal immune responses in healthy immunocompetent mice and human peripheral blood mononuclear cells. These results demonstrate that bioengineered let-7c is a promising molecule for advanced HCC therapy, and liposomal polyplex is a superior modality for in vivo RNA delivery.

Pubmed