基因重组间充质干细胞作为肿瘤靶向递送载体的研究进展
[Research progress of gene recombinant mesenchymal stem cells as tumor targeting delivery vehicles].
作者信息
Zhang Tian-Yuan, Hu Yu-Lan, Liang Wen-Quan, Gao Jian-Qing
机构信息
Institute of Phamaceutics, Zhejiang University, Hangzhou 310058, China.
出版信息
Yao Xue Xue Bao. 2013 Aug;48(8):1209-20.
The applications of targeting gene delivery systems in tumor therapy have attracted extensive attention of researchers in recent years, as they can selectively deliver the therapeutic gene to tumor sites, improve the success rate of gene therapy and reduce the side effects. Therefore, design and development of novel gene delivery vehicles have been a hot area of current research. Recent studies have shown that mesenchymal stem cells (MSCs) have the ability to migrate towards and engraft into the tumor sites. Therefore, these properties make them a great hope for efficient targeted-delivery vehicles in cancer gene therapy. In this review, we examine the promising of utilization of MSCs as a targeted-delivery vehicle for cancer gene therapy, and summarize various challenges and concerns regarding this therapy.
近年来,靶向基因递送系统在肿瘤治疗中的应用引起了研究人员的广泛关注,因为它们可以将治疗性基因选择性地递送至肿瘤部位,提高基因治疗的成功率并减少副作用。因此,新型基因递送载体的设计与开发一直是当前研究的热点领域。最近的研究表明,间充质干细胞(MSCs)具有向肿瘤部位迁移并植入的能力。因此,这些特性使其成为癌症基因治疗中高效靶向递送载体的巨大希望。在本综述中,我们研究了利用间充质干细胞作为癌症基因治疗靶向递送载体的前景,并总结了关于这种治疗的各种挑战和问题。