Antitumor Activity of Anti-miR-21 Delivered through Lipid Nanoparticles

  • Adv Healthc Mater. 2023 Jan;12(6):e2202412. doi: 10.1002/adhm.202202412.
Zhongkun Zhang  1 Yirui Huang  1 Jing Li  2 Fei Su  2 Jimmy Chun-Tien Kuo  1 Yingwen Hu  3 Xiaobin Zhao  3 Robert J Lee  1
Affiliations
  • 1. Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, 500 W 12th Avenue, Columbus, OH, 43210, USA.
  • 2. Zhejiang Haichang Biotechnology Co., Ltd., Hangzhou, Zhejiang, 310000, P. R. China.
  • 3. The Whiteoak Group, Inc., Rockville, MD, 20855, USA.
Abstract

The ability of lipid nanoparticles (LNPs) to deliver nucleic acids have shown a great therapeutic potential to treat a variety of diseases. Here, an optimized formulation of QTsome lipid nanoparticles (QTPlus) is utilized to deliver an anti-miR-21 (AM21) against Cancer. The miR-21 downstream gene regulation and antitumor activity is evaluated using mouse and human Cancer cells and macrophages. The antitumor activity of QTPlus encapsulating AM21 (QTPlus-AM21) is further evaluated in combination with erlotinib and atezolizumab (ATZ). QTPlus-AM21 demonstrates a superior miR-21-dependent gene regulation and eventually inhibits A549 non-small cell lung Cancer growth in vitro. QTPlus-AM21 further induces chemo-sensitization of A549 cells to erlotinib with a combination index of 0.6 in inhibiting A549 cell growth. When systemically administers to MC38 tumor-bearing mouse model, QTPlus-AM21 exhibits an antitumor immune response with over 80% tumor growth inhibition (TGI%) and over twofold and fourfold PD-1 and PD-L1 upregulation in tumors and spleens. The combination therapy of QTPlus-AM21 and ATZ further shows a higher antitumor response (TGI% over 90%) and successfully increases M1 macrophages and CD8 T cells into TME. This study provides new insights into the antitumor mechanism of AM21 and shows great promise of QTPlus-AM21 in combination with chemotherapies and immunotherapies.

Keywords
cancer therapy; immunoregulation; lipid nanoparticles; oligonucleotides.
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