Ding Yuan, Wang Chenyang, Sun Zhongquan, Wu Yingsheng, You Wanlu, Mao Zhengwei, Wang Weilin
Department of Hepatobiliary and Pancreatic Surgery, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
Key Laboratory, Precision Diagnosis and Treatment for Hepatobiliary and Pancreatic Tumor of Zhejiang Province, Hangzhou 310009, China.
Pharmaceutics. 2021 Jun 21;13(6):913. doi: 10.3390/pharmaceutics13060913.
Due to their "tumor homing" and "immune privilege" characteristics, the use of mesenchymal stem cells (MSCs) has been proposed as a novel tool against cancer. MSCs are genetically engineered in vitro and then utilized to deliver tumoricidal agents, including prodrugs and bioactive molecules, to tumors. The genetic modification of MSCs can be achieved by various vectors, and in most cases viral vectors are used; however, viruses may be associated with carcinogenesis and immunogenicity, restricting their clinical translational potential. As such, nonviral vectors have emerged as a potential solution to address these limitations and have gradually attracted increasing attention. In this review, we briefly revisit the current knowledge about MSC-based cancer gene therapy. Then, we summarize the advantages and challenges of nonviral vectors for MSC transfection. Finally, we discuss recent advances in the development of new nonviral vectors, which have provided promising strategies to overcome obstacles in the gene modulation of MSCs.
由于间充质干细胞(MSCs)具有“肿瘤归巢”和“免疫特权”特性,其被提议作为一种新型抗癌工具。间充质干细胞在体外进行基因工程改造,然后用于将包括前药和生物活性分子在内的杀肿瘤剂递送至肿瘤。间充质干细胞的基因改造可通过多种载体实现,大多数情况下使用病毒载体;然而,病毒可能与致癌作用和免疫原性相关,限制了它们的临床转化潜力。因此,非病毒载体已成为解决这些局限性的潜在解决方案,并逐渐引起了越来越多的关注。在本综述中,我们简要回顾了目前关于基于间充质干细胞的癌症基因治疗的知识。然后,我们总结了非病毒载体用于间充质干细胞转染的优势和挑战。最后,我们讨论了新型非病毒载体开发的最新进展,这些进展提供了有前景的策略来克服间充质干细胞基因调控中的障碍。