干细胞信号通路的药理调控及其治疗应用。

IF 7.1 2区 医学 Q1 CELL & TISSUE ENGINEERING
Sulaiman Mohammed Alnasser, Abdulrahman Saleh Alrobian, Mohammad Salem Alfayez, Omar Tuwayli Almutairi, Saud Saeed Almutairi, Talal Sami Alkeraidees
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引用次数: 0

摘要

干细胞具有非凡的自我更新和分化能力,处于治疗的前沿,为修复组织、癌症治疗和治疗退行性疾病提供了有希望的解决方案。干细胞命运受Hedgehog、TGF-β、Wnt、Hippo、FGF、BMP和Notch等关键信号通路的严格调控,这些通路成为精准干预的首要目标。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了临床成功。通过增强干细胞存活、指导分化和调节干细胞生态位,药理学策略正在成为克服这些障碍的有力工具。小分子可以激活内源性干细胞,减少移植的需要,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治疗方法。这为更安全、更有效和个性化的治疗铺平了道路。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。综合个性化医疗、药理学调节和组织工程的多学科方法是解决这些限制的关键。利用干细胞疗法推进研究和完善以前的策略,有望彻底改变再生和肿瘤医学,为广泛的疾病提供更有针对性和可持续的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological modulation of stem cells signaling pathway for therapeutic applications.

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.

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来源期刊
Stem Cell Research & Therapy
Stem Cell Research & Therapy CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
13.20
自引率
8.00%
发文量
525
审稿时长
1 months
期刊介绍: Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.
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