← 返回

间充质干细胞恶性转化的分子展望:细胞治疗中的一个问题

英文原题:Molecular Prospective on Malignant Transformation of Mesenchymal Stem Cells: An Issue in Cell Therapy.

查看英文原题

Molecular Prospective on Malignant Transformation of Mesenchymal Stem Cells: An Issue in Cell Therapy.

PubMed 2024/06/01(内容时间) Cell Reprogram Q2 · IF 2.7(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

间充质干细胞疗法发展迅速,有望用于多种疾病治疗。间充质干细胞可从不同组织分离,具有自我更新和分化能力,并能分泌细胞因子及营养因子、形成再生微环境和调节免疫。尽管已有多种疾病的临床试验,但细胞恶性转化的可能性引发安全顾虑。实验模型显示,移植后血液系统恶性肿瘤和致癌发生率可能升高。其机制复杂且尚未完全阐明,可能涉及特定信号分子及细胞行为调控通路改变;自发或受刺激的转化机制还包括细胞融合、融合蛋白及肿瘤微环境因素。要确保疗法安全有效,必须解决恶性转化风险。本文综述间充质干细胞恶性转化的潜在机制。

展开英文摘要原文

Mesenchymal stem cell (MSCs) therapy, as a rapidly developing area of medicine, holds great promise for the treatment of a variety of medical conditions. MSCs are multipotent stem cells that can be isolated from various tissues and could self-renew and differentiate. They secrete cytokines and trophic factors that create a regenerative microenvironment and have immunomodulatory properties. Although clinical trials have been conducted with MSCs in various diseases, concerns regarding the possibility of malignant transformation of these cells have been raised. The studies showed a higher rate of hematological malignancy and carcinogenesis in experimental models after MSC transplantation.

The mechanisms underlying malignant transformation of MSCs are complex and not fully understood, but they are believed to involve the presence of special signaling molecules and alterations in cell behavior regulation pathways.

Possible pathways that lead to MSCs' oncogenic transformation occur through two mechanisms: spontaneous and stimulated malignant transformation, including cell fusion, fusion proteins, and the tumor microenvironment. MSC-based therapies have the potential to revolutionize medicine, and addressing the issue of malignancy is crucial to ensure their safety and efficacy.

Therefore, the purpose of the present review is to summarize the potential mechanisms of the malignant transformation of MSCs. [Figure: see text].

论文信息

作者
Kaviani M、Soleimanian S、Keshtkar S、Azarpira N、Asvar Z、Pakbaz S
第一作者单位
Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.Iran
通讯作者单位
Department of Laboratory Medicine and Pathobiology, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.Canada
文献类型
综述
期刊
Cellular reprogramming2024 Jun
原文标识
PubMed 38917438 · DOI 10.1089/cell.2024.0026