软骨细胞
调节器
衰老
骨关节炎
癌症研究
发病机制
双重角色
医学
生物
调解人
细胞衰老
平衡
软骨
FOXO3公司
干细胞
细胞生物学
生物信息学
细胞周期进展
信号转导
对偶(语法数字)
NF-κB
基因
作者
Chan Wang,Jun Zhou,Lie Chen,Changyan Ma,Zhan Dong,Dengshun Miao
标识
DOI:10.1186/s13578-026-01541-y
摘要
This study establishes lncRNA HOXC-AS3 as a key regulator of chondrocyte homeostasis that mitigates OA progression via dual mechanisms-miR-615-3p sponging and RRBP1 interaction-both of which maintain CIT expression. These findings advance the understanding of the molecular networks underlying OA pathogenesis and underscore HOXC-AS3 and its downstream signaling axis as promising therapeutic targets for OA intervention.
科研通智能强力驱动
Strongly Powered by AbleSci AI