Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Physiol.

Sec. Skeletal Physiology

Volume 16 - 2025 | doi: 10.3389/fphys.2025.1650380

Identification and Functional Analysis of Circular RNAs in Intervertebral Disc Lesion Tissues from Spinal Tuberculosis Patients

Provisionally accepted
Linan  WangLinan Wang1,2Xingyu  DuanXingyu Duan1,2Yuliang  QuYuliang Qu2Zhiyun  ShiZhiyun Shi1Xu  ZHANGXu ZHANG1Zongqiang  YangZongqiang Yang1Yingchao  GaoYingchao Gao2*Ningkui  NiuNingkui Niu1*
  • 1General Hospital of Ningxia Medical University, Yinchuan, China
  • 2Ningxia Medical University, Yinchuan, China

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

Background: Spinal tuberculosis (STB) is characterized by an insidious onset, nonspecific clinical manifestations, and diagnostic challenges in early stages. Circular RNAs (circRNAs), a class of stable single-stranded endogenous RNAs with covalently closed-loop structures, play crucial regulatory roles in various biological processes. However, their involvement in STB pathogenesis remains largely unexplored.We collected intervertebral disc tissue specimens and peripheral blood samples from STB patients. CircRNAs sequencing was performed on three representative lesion tissues, followed by comprehensive screening and validation in both tissue and blood samples to elucidate the functional mechanisms of circRNAs in STB.Results: Chip sequencing indicated that a total of 1,396 circRNAs were differentially expressed (fold change > 2, P < 0.05). Among them, 757 circRNAs were upregulated, while 639 were downregulated.GO analysis of the parental genes of these differentially expressed circRNAs demonstrated that they were predominantly involved in cellular protein catabolic processes, GTPase binding, covalent chromatin modification, histone modification, and other processes.KEGG pathway analysis revealed that these genes were mainly enriched in signal pathways such as protein processing in the endoplasmic reticulum, apoptosis, and proteolysis. Validation in peripheral blood samples showed that the expressions of hsa_circ_0001021, hsa_circ_0043898, and hsa_circ_0093669 were significantly higher in the preoperative group than in the control group (P < 0.05). Moreover, the expression levels of these circRNAs decreased at 6 months and 1 year postoperatively compared to the preoperative levels. ROC curve analysis suggested that these circRNAs could serve as promising diagnostic biomarkers for STB in academic research scenarios.The differentially expressed circRNAs identified in intervertebral disc lesions of STB patients demonstrate significant involvement in disease pathogenesis, positioning them as promising candidates for both diagnostic and therapeutic targeting. Specifically, hsa_circ_0001021, hsa_circ_0043898, and hsa_circ_0093669 exhibit robust potential as peripheral blood-based diagnostic biomarkers for STB. When combined with conventional inflammatory markers ESR and CRP, these circRNAs significantly enhance diagnostic accuracy. Furthermore, longitudinal monitoring revealed their unique value in postoperative therapeutic evaluation, with expression levels showing strong correlation with treatment response.

Keywords: spinal tuberculosis, circular RNA, Intervertebral Disc, Gene chip, Pathogenesis

Received: 19 Jun 2025; Accepted: 19 Aug 2025.

Copyright: © 2025 Wang, Duan, Qu, Shi, ZHANG, Yang, Gao and Niu. 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:
Yingchao Gao, Ningxia Medical University, Yinchuan, China
Ningkui Niu, General Hospital of Ningxia Medical University, Yinchuan, China

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.