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Protein liposomes-mediated targeted acetylcholinesterase gene delivery for effective liver cancer therapy.

AbstractBACKGROUND:
Effective methods to deliver therapeutic genes to solid tumors and improve their bioavailability are the main challenges of current medical research on gene therapy. The development of efficient non-viral gene vector with tumor-targeting has very important application value in the field of cancer therapy. Proteolipid integrated with tumor-targeting potential of functional protein and excellent gene delivery performance has shown potential for targeted gene therapy.
RESULTS:
Herein, we prepared transferrin-modified liposomes (Tf-PL) for the targeted delivery of acetylcholinesterase (AChE) therapeutic gene to liver cancer. We found that the derived Tf-PL/AChE liposomes exhibited much higher transfection efficiency than the commercial product Lipo 2000 and shown premium targeting efficacy to liver cancer SMMC-7721 cells in vitro. In vivo, the Tf-PL/AChE could effectively target liver cancer, and significantly inhibit the growth of liver cancer xenografts grafted in nude mice by subcutaneous administration.
CONCLUSIONS:
This study proposed a transferrin-modified proteolipid-mediated gene delivery strategy for targeted liver cancer treatment, which has a promising potential for precise personalized cancer therapy.
AuthorsKai Wang, Fusheng Shang, Dagui Chen, Tieliu Cao, Xiaowei Wang, Jianpeng Jiao, Shengli He, Xiaofei Liang
JournalJournal of nanobiotechnology (J Nanobiotechnology) Vol. 19 Issue 1 Pg. 31 (Jan 22 2021) ISSN: 1477-3155 [Electronic] England
PMID33482834 (Publication Type: Journal Article)
Chemical References
  • Liposomes
  • Transferrin
  • Acetylcholinesterase
Topics
  • Acetylcholinesterase (genetics)
  • Animals
  • Cell Line, Tumor
  • Female
  • Gene Transfer Techniques
  • Genetic Therapy
  • Humans
  • Liposomes (chemistry)
  • Liver Neoplasms (genetics, therapy)
  • Mice, Inbred BALB C
  • Mice, Nude
  • Plasmids (administration & dosage, genetics, therapeutic use)
  • Transfection
  • Transferrin (chemistry)

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