Nowakowski Adam, Drela Katarzyna, Rozycka Justyna, Janowski Miroslaw, Lukomska Barbara
1 NeuroRepair Department, Mossakowski Medical Research Centre , Polish Academy of Sciences, Warsaw, Poland .
2 Division of MR Research, Russel H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine , Baltimore, Maryland.
Stem Cells Dev. 2016 Oct;25(20):1513-1531. doi: 10.1089/scd.2016.0120. Epub 2016 Sep 7.
Cell-based gene therapy holds a great promise for the treatment of human malignancy. Among different cells, mesenchymal stem cells (MSCs) are emerging as valuable anti-cancer agents that have the potential to be used to treat a number of different cancer types. They have inherent migratory properties, which allow them to serve as vehicles for delivering effective therapy to isolated tumors and metastases. MSCs have been engineered to express anti-proliferative, pro-apoptotic, and anti-angiogenic agents that specifically target different cancers. Another field of interest is to modify MSCs with the cytokines that activate pro-tumorigenic immunity or to use them as carriers for the traditional chemical compounds that possess the properties of anti-cancer drugs. Although there is still controversy about the exact function of MSCs in the tumor settings, the encouraging results from the preclinical studies of MSC-based gene therapy for a large number of tumors support the initiation of clinical trials.
基于细胞的基因疗法在治疗人类恶性肿瘤方面具有巨大潜力。在不同细胞中,间充质干细胞(MSCs)正成为有价值的抗癌剂,有可能用于治疗多种不同类型的癌症。它们具有固有的迁移特性,这使其能够作为载体,将有效疗法传递至孤立的肿瘤和转移灶。间充质干细胞已被改造以表达特异性靶向不同癌症的抗增殖、促凋亡和抗血管生成因子。另一个感兴趣的领域是用激活促肿瘤免疫的细胞因子修饰间充质干细胞,或将它们用作具有抗癌药物特性的传统化合物的载体。尽管间充质干细胞在肿瘤环境中的确切功能仍存在争议,但基于间充质干细胞的基因疗法针对大量肿瘤的临床前研究取得的令人鼓舞的结果支持开展临床试验。