4.6 Article

Tumor regression following intravenous administration of lactoferrin- and lactoferricin-bearing dendriplexes

期刊

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nano.2015.04.006

关键词

Cancer therapy; Gene delivery; Dendrimer; Lactoferrin; Lactoferricin

资金

  1. Medical Research Council research grant
  2. Wellcome Trust [ME0442]
  3. Cunningham Trust
  4. Saudi Cultural Bureau and Taif University (Kingdom of Saudi Arabia)
  5. MRC [MR/J007129/1] Funding Source: UKRI
  6. Medical Research Council [MR/J007129/1] Funding Source: researchfish

向作者/读者索取更多资源

The possibility of using gene therapy for the treatment of cancer is limited by the lack of safe, intravenously administered delivery systems able to selectively deliver therapeutic genes to tumors. In this study, we investigated if the conjugation of the polypropylenimine dendrimer to lactoferrin and lactoferricin, whose receptors are overexpressed on cancer cells, could result in a selective gene delivery to tumors and a subsequently enhanced therapeutic efficacy. The conjugation of lactoferrin and lactoferricin to the dendrimer significantly increased the gene expression in the tumor while decreasing the non-specific gene expression in the liver. Consequently, the intravenous administration of the targeted dendriplexes encoding TNF alpha led to the complete suppression of 60% of A431 tumors and up to 50% of B16-F10 tumors over one month. The treatment was well tolerated by the animals. These results suggest that these novel lactoferrin-and lactoferricin-bearing dendrimers are promising gene delivery systems for cancer therapy. From the Clinical Editor: Specific targeting of cancer cells should enhance the delivery of chemotherapeutic agents. This is especially true for gene delivery. In this article, the authors utilized a dendrimer-based system and conjugated this with lactoferrin and lactoferricin to deliver anti-tumor genes. The positive findings in animal studies should provide the basis for further clinical studies. (C) 2015 The Authors. Published by Elsevier Inc.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据