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用于治疗应用的干细胞信号通路的药理学调节。

Pharmacological modulation of stem cells signaling pathway for therapeutic applications.

作者信息

Alnasser Sulaiman Mohammed, Alrobian Abdulrahman Saleh, Alfayez Mohammad Salem, Almutairi Omar Tuwayli, Almutairi Saud Saeed, Alkeraidees Talal Sami

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, Qassim University, 51452, Qassim, Saudi Arabia.

College of Pharmacy, Qassim University, 51452, Buraydah, Qassim, Saudi Arabia.

出版信息

Stem Cell Res Ther. 2025 Jul 1;16(1):327. doi: 10.1186/s13287-025-04438-8.

Abstract

Stem cells have an exceptional capacity for self-renewal and differentiation and are at the forefront of therapeutics, offering promising solutions for repairing tissues, cancer treatment and the cure of degenerative diseases. Stem cell fate is tightly regulated by key signaling pathways like Hedgehog, TGF-β, Wnt, Hippo, FGF, BMP and Notch, making these pathways prime targets for precision interventions. Despite significant advancements, challenges such as immune rejection, tumorigenesis, and inefficient tissue integration continue to limit clinical success. Pharmacological strategies are emerging as powerful tools to overcome these barriers by enhancing stem cell survival, directing differentiation, and modulating the stem cell niche. Small molecules can activate endogenous stem cells, reducing the need for transplantation while promoting in situ regeneration. Additionally, advancements in gene-editing technologies and biomaterials are further refining stem cell-based therapies. This paves the way for safer, more effective, and personalized therapies. Nevertheless, transforming these innovations into clinical practice entails overcoming regulatory hurdles, optimizing delivery methods, and ensuring long-term safety and efficacy. A multidisciplinary approach integrating personalized medicine, pharmacological modulation, and tissue engineering holds the key to addressing these limitations. Advancing research and refining previous strategies utilizing stem cell therapies has the prospective to revolutionize regenerative and onco-medicine, providing more targeted and sustainable treatment options for a wide range of diseases.

摘要

干细胞具有非凡的自我更新和分化能力,处于治疗领域的前沿,为组织修复、癌症治疗和退行性疾病的治愈提供了有前景的解决方案。干细胞命运受到刺猬信号通路(Hedgehog)、转化生长因子-β(TGF-β)、Wnt、河马信号通路(Hippo)、成纤维细胞生长因子(FGF)、骨形态发生蛋白(BMP)和Notch等关键信号通路的严格调控,使这些通路成为精准干预的主要靶点。尽管取得了重大进展,但免疫排斥、肿瘤发生和组织整合效率低下等挑战仍然限制着临床成功。药理学策略正成为克服这些障碍的有力工具,通过提高干细胞存活率、引导分化和调节干细胞微环境来实现。小分子可以激活内源性干细胞,减少移植需求,同时促进原位再生。此外,基因编辑技术和生物材料的进步正在进一步完善基于干细胞的疗法。这为更安全、更有效和个性化的疗法铺平了道路。然而,将这些创新转化为临床实践需要克服监管障碍、优化给药方法,并确保长期安全性和有效性。整合个性化医学、药理学调节和组织工程的多学科方法是解决这些局限性的关键。推进利用干细胞疗法的研究并完善先前的策略有望彻底改变再生医学和肿瘤医学,为广泛的疾病提供更有针对性和可持续的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1003/12210473/1b1e99b84cc6/13287_2025_4438_Fig1_HTML.jpg

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