4.6 Article

Modified nanoparticle mediated IL-12 immunogene therapy for colon cancer

Journal

NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE
Volume 13, Issue 6, Pages 1993-2004

Publisher

ELSEVIER
DOI: 10.1016/j.nano.2017.04.006

Keywords

Colorectal cancer; Immunotherapy; Interleukin-12; Nanoparticles

Funding

  1. National Natural Science Foundation of China [NSFC81502165]
  2. Sichuan University Outstanding Young Scholars Research Fund [2016SCU04A04]

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For the past few years, immunotherapy has recently shown considerable clinical benefit in CRC therapy, and the application of immunologic therapies in cancer treatments continues to increase perennially. Interleukin-12, an ideal candidate for tumor immunotherapy, could activate both innate and adaptive immunities. In this study, we developed a novel gene delivery system with a self-assembly method by MPEG-PLA and DOTAP( DMP) with zeta-potential value of 38.5 mV and size of 37.5 nm. The supernatant of lymphocytes treated with supernatant from Ct26 transfected pIL12 with DMP could inhibit Ct26 cells growth ex vivo. Treatment of tumor-bearing mice with DMPpIL12 complex has significantly inhibited tumor growth at both the subcutaneous and peritoneal model in vivo by inhibiting angiogenesis, promoting apoptosis and reducing proliferation. The IL-12 plasmid and DMP complex may be used to treat the colorectal cancer in clinical as a new drug. (C) 2017 Elsevier Inc. All rights reserved.

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