Triazine-modified dendrimer for efficient TRAIL gene therapy in osteosarcoma

  • Yu Wang
  • , Lei Li
  • , Naimin Shao
  • , Zhiqi Hu
  • , Hui Chen
  • , Leqin Xu
  • , Changping Wang
  • , Yiyun Cheng*
  • , Jianru Xiao
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

Abstract

Osteosarcoma is a high-grade malignant bone tumor that usually develops in the teenagers. Despite improvement in therapy, the five-year survival rate is poor for patients not responding to treatment or with metastases. Tumor necrosis factor (TNF) related apoptosis inducing ligand (TRAIL) gene therapy is a new strategy in the treatment of cancers, however, the lack of efficient and low toxic vectors remains the major obstacle in TRAIL gene therapy. In this study, a triazine-modified dendrimer G5-DAT66 was synthesized and used as a vector for TRAIL gene therapy in vitro and in vivo. The material shows much higher transfection efficacy on osteosarcoma MG-63 cell line than commercial transfection reagents such as Lipofectamine 2000 and SuperFect. It effectively induces apoptosis in MG-63 cells and three-dimensional MG-63 cell cultures when delivering a TRAIL plasmid. In vivo studies further prove that G5-DAT66 efficiently transfects TRAIL plasmid in tumors and inhibits tumor growth in osteosarcoma-bearing mice. These results suggest that triazine-modified dendrimer has promising potential for TRAIL gene therapy in osteosarcoma.

Original languageEnglish
Pages (from-to)115-124
Number of pages10
JournalActa Biomaterialia
Volume17
DOIs
StatePublished - 15 Apr 2015

Keywords

  • Dendrimer
  • Gene therapy
  • Osteosarcoma
  • TRAIL

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