Targeting the mTOR-Autophagy Axis: Unveiling Therapeutic Potentials in Osteoporosis.

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Biomolecules Pub Date : 2024-11-15 DOI:10.3390/biom14111452
Rongjin Chen, Chenhui Yang, Fei Yang, Ao Yang, Hefang Xiao, Bo Peng, Changshun Chen, Bin Geng, Yayi Xia
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Abstract

Osteoporosis (OP) is a widespread age-related disorder marked by decreased bone density and increased fracture risk, presenting a significant public health challenge. Central to the development and progression of OP is the dysregulation of the mechanistic target of the rapamycin (mTOR)-signaling pathway, which plays a critical role in cellular processes including autophagy, growth, and proliferation. The mTOR-autophagy axis is emerging as a promising therapeutic target due to its regulatory capacity in bone metabolism and homeostasis. This review aims to (1) elucidate the role of mTOR signaling in bone metabolism and its dysregulation in OP, (2) explore the interplay between mTOR and autophagy in the context of bone cell activity, and (3) assess the therapeutic potential of targeting the mTOR pathway with modulators as innovative strategies for OP treatment. By examining the interactions among autophagy, mTOR, and OP, including insights from various types of OP and the impact on different bone cells, this review underscores the complexity of mTOR's role in bone health. Despite advances, significant gaps remain in understanding the detailed mechanisms of mTOR's effects on autophagy and bone cell function, highlighting the need for comprehensive clinical trials to establish the efficacy and safety of mTOR inhibitors in OP management. Future research directions include clarifying mTOR's molecular interactions with bone metabolism and investigating the combined benefits of mTOR modulation with other therapeutic approaches. Addressing these challenges is crucial for developing more effective treatments and improving outcomes for individuals with OP, thereby unveiling the therapeutic potentials of targeting the mTOR-autophagy axis in this prevalent disease.

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以 mTOR-Autophagy 轴为靶点:揭示骨质疏松症的治疗潜力。
骨质疏松症(Osteoporosis,OP)是一种广泛存在的与年龄有关的疾病,其特点是骨密度降低和骨折风险增加,给公共卫生带来了重大挑战。雷帕霉素机械靶标(mTOR)信号通路的失调是骨质疏松症发生和发展的核心原因,它在自噬、生长和增殖等细胞过程中发挥着至关重要的作用。mTOR-自噬轴在骨代谢和稳态中具有调节能力,因此正在成为一个有前景的治疗靶点。本综述旨在:(1) 阐明 mTOR 信号在骨代谢中的作用及其在 OP 中的失调;(2) 探讨 mTOR 和自噬在骨细胞活动中的相互作用;(3) 评估针对 mTOR 通路使用调节剂作为 OP 治疗创新策略的治疗潜力。通过研究自噬、mTOR 和 OP 之间的相互作用,包括从各种类型的 OP 及其对不同骨细胞的影响中获得的见解,本综述强调了 mTOR 在骨骼健康中作用的复杂性。尽管取得了进展,但在了解 mTOR 对自噬和骨细胞功能影响的详细机制方面仍存在很大差距,这突出表明需要进行全面的临床试验,以确定 mTOR 抑制剂在 OP 治疗中的疗效和安全性。未来的研究方向包括阐明 mTOR 与骨代谢之间的分子相互作用,以及研究 mTOR 调节与其他治疗方法的综合疗效。应对这些挑战对于开发更有效的治疗方法和改善 OP 患者的预后至关重要,从而揭示针对这一流行疾病的 mTOR-autophagy 轴的治疗潜力。
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
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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