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REVIEW article

Front. Cell Dev. Biol.

Sec. Signaling

Volume 13 - 2025 | doi: 10.3389/fcell.2025.1643255

Non-coding RNAs mediate mechanical load-regulating bone metabolic homeostasis

Provisionally accepted
  • 1Liaoning Normal University, Dalian, China
  • 2Zhuhai College of Science and Technology, Zhuhai, China
  • 3Shenyang Sport University, Shenyang, China

The final, formatted version of the article will be published soon.

Bone, as a highly active organ, relies on dynamic mechanical stimulation for its continuous remodeling and regeneration. Mechanotransduction, the regulatory process through which mechanical forces are converted into biochemical signals, involves intricate interactions within and between cells and their extracellular environment, playing a crucial role in maintaining bone metabolic homeostasis. The complexity of this process stems primarily from the diversity of input signals and the precise regulation of downstream signaling cascades. In recent years, studies have revealed that non-coding RNAs (ncRNAs) play a key role in mediating the regulation of bone metabolism by mechanical loading. This review elaborates on how mechanosensitive ncRNAs participate in the regulation of bone mechanotransduction signaling pathways. Furthermore, we explore how different mechanical stimuli (such as loading and unloading) influence skeletal adaptive responses by modulating the expression of ncRNAs. Thus, this article not only provides novel perspectives on the mechanical regulatory functions of ncRNAs in bone metabolism, but also offers new strategies for preventing and treating bone metabolic disorders caused by mechanical disuse.

Keywords: Bone, Mechanical load, non-coding RNA, micro RNA, bone disease

Received: 08 Jun 2025; Accepted: 13 Oct 2025.

Copyright: © 2025 Huang, Chang and Yi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Xuejie Yi, yixuejie8387@163.com

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