Xu-Yong Sun, Jiang Nong, Ke Qin, Institute of Transplant Medicine, 303 Hospital of Chinese People's Liberation Army, Nanning 530021, The Guangxi Zhuang Autonomous Region, China.
World J Stem Cells. 2011 Nov 26;3(11):96-103. doi: 10.4252/wjsc.v3.i11.96.
Cancer remains one of the leading causes of mortality and morbidity throughout the world. To a significant extent, current conventional cancer therapies are symptomatic and passive in nature. The major obstacle to the development of effective cancer therapy is believed to be the absence of sufficient specificity. Since the discovery of the tumor-oriented homing capacity of mesenchymal stem cells (MSCs), the application of specific anticancer gene-engineered MSCs has held great potential for cancer therapies. The dual-targeted strategy is based on MSCs' capacity of tumor-directed migration and incorporation and in situ expression of tumor-specific anticancer genes. With the aim of translating bench work into meaningful clinical applications, we describe the tumor tropism of MSCs and their use as therapeutic vehicles, the dual-targeted anticancer potential of engineered MSCs and a putative personalized strategy with anticancer gene-engineered MSCs.
癌症仍然是全世界导致死亡和发病的主要原因之一。在很大程度上,目前的常规癌症疗法在性质上是对症的和被动的。人们认为,发展有效癌症疗法的主要障碍是缺乏足够的特异性。自从发现间充质干细胞(MSCs)具有针对肿瘤的归巢能力以来,应用特定的抗癌基因工程 MSC 治疗癌症具有很大的潜力。双靶向策略基于 MSCs 向肿瘤迁移和整合以及原位表达肿瘤特异性抗癌基因的能力。为了将基础研究转化为有意义的临床应用,我们描述了 MSCs 的肿瘤趋向性及其作为治疗载体的用途、工程 MSC 的双靶向抗癌潜力以及用抗癌基因工程 MSC 的个体化策略。