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诱导多能干细胞衍生的间充质干细胞:向个性化治疗迈进的一大步。

Induced pluripotent stem cell-derived mesenchymal stem cells: A leap toward personalized therapies.

作者信息

Whitt Jason, Vallabhaneni Krishna C, Penfornis Patrice, Pochampally Radhika

机构信息

Cancer Institute and Department of Biochemistry of University of Mississippi Medical Center, Jackson, MS 39216, USA.

出版信息

Curr Stem Cell Res Ther. 2016;11(2):141-8. doi: 10.2174/1574888x10666151001114321.

Abstract

Mesenchymal Stem/stromal cell (MSCs) transplantation procedures have been used since the 1960's to treat leukemia and other diseases, but due to the risks involved only patients with life threatening illnesses were typically subjected to the transplantation procedure until the last decade. Recent advancements in transplantation techniques have made it more feasible to use it for non-life-threatening diseases. However, the potential uses for stem cells are still limited by their rarity, and, in the case of allogeneic transplants, graft-vs.-host complications. An evolving alternative to conventional stem cell therapies is induced pluripotent stem-cell derived mesenchymal stem/stromal cells (iPSC- MSCs), which have a multi-lineage potential comparable to conventionally acquired MSCs with the added benefit of being less immunoreactive. However there are still many hurdles left to be overcome before they can be used regularly for personalized therapies. This review will focus on recent advancements that have been made regarding the role MSCs play in tumor development and the potential uses iPSC-MSCs may have in future cancer treatment.

摘要

自20世纪60年代以来,间充质干/基质细胞(MSCs)移植程序就已被用于治疗白血病和其他疾病,但由于存在风险,直到过去十年,通常只有患有危及生命疾病的患者才会接受移植程序。移植技术的最新进展使其用于非危及生命疾病变得更加可行。然而,干细胞的潜在用途仍然受到其稀缺性的限制,并且在同种异体移植的情况下,还存在移植物抗宿主并发症。一种替代传统干细胞疗法的不断发展的方法是诱导多能干细胞衍生的间充质干/基质细胞(iPSC-MSCs),其具有与传统获得的MSCs相当的多谱系潜能,并且具有免疫反应性较低的额外优势。然而,在它们能够常规用于个性化治疗之前,仍有许多障碍有待克服。本综述将重点关注MSCs在肿瘤发展中所起作用的最新进展以及iPSC-MSCs在未来癌症治疗中可能的潜在用途。

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