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

IF 1.2 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Maryam Kaviani, Saeede Soleimanian, Somayeh Keshtkar, Negar Azarpira, Zahra Asvar, Sara Pakbaz
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引用次数: 0

Abstract

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].

间充质干细胞恶性转化的分子前瞻:细胞疗法中的一个问题。
间充质干细胞(MSCs)疗法是一个快速发展的医学领域,在治疗各种疾病方面前景广阔。间充质干细胞是从各种组织中分离出来的多能干细胞,可以自我更新和分化。它们能分泌细胞因子和营养因子,创造再生微环境,并具有免疫调节特性。虽然已经开展了间充质干细胞治疗各种疾病的临床试验,但人们对这些细胞可能发生恶性转化表示担忧。研究表明,在实验模型中,间充质干细胞移植后血液恶性肿瘤和癌变的发生率较高。间充质干细胞恶性转化的机制复杂,尚未完全明了,但据信涉及特殊信号分子的存在和细胞行为调节途径的改变。导致间充质干细胞致癌转化的可能途径有两种:自发和受刺激的恶性转化,包括细胞融合、融合蛋白和肿瘤微环境。基于间充质干细胞的疗法有可能给医学带来革命性的变化,而解决恶性转化问题对于确保其安全性和有效性至关重要。因此,本综述旨在总结间充质干细胞恶性转化的潜在机制。[图:见正文]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular reprogramming
Cellular reprogramming CELL & TISSUE ENGINEERING-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
CiteScore
2.50
自引率
6.20%
发文量
37
审稿时长
3 months
期刊介绍: Cellular Reprogramming is the premier journal dedicated to providing new insights on the etiology, development, and potential treatment of various diseases through reprogramming cellular mechanisms. The Journal delivers information on cutting-edge techniques and the latest high-quality research and discoveries that are transforming biomedical research. Cellular Reprogramming coverage includes: Somatic cell nuclear transfer and reprogramming in early embryos Embryonic stem cells Nuclear transfer stem cells (stem cells derived from nuclear transfer embryos) Generation of induced pluripotent stem (iPS) cells and/or potential for cell-based therapies Epigenetics Adult stem cells and pluripotency.
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