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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
  • *此作品的通讯作者
  • Changzheng Hospital
  • Wenzhou Medical University
  • East China Normal University

科研成果: 期刊稿件文章同行评审

摘要

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.

源语言英语
页(从-至)115-124
页数10
期刊Acta Biomaterialia
17
DOI
出版状态已出版 - 15 4月 2015

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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