肺结核
细胞因子信号抑制因子1
发病机制
免疫学
医学
免疫系统
基因
生物
病理
遗传学
抑制器
作者
Tuo Liang,Jiarui Chen,Guoyong Xu,Zide Zhang,Jiang Xue,Huilan Zeng,Jie Jiang,Tianyou Chen,Zhaojie Qin,Hao Li,Zhen Ye,Yunfeng Nie,Chong Liu,Xinli Zhan
出处
期刊:Tuberculosis
[Elsevier]
日期:2022-01-01
卷期号:132: 102140-102140
被引量:14
标识
DOI:10.1016/j.tube.2021.102140
摘要
This study was aimed to reveal the role of ferroptosis in tuberculosis infection. To elucidate the ferroptosis-related DEGs, GEO datasets associated with tuberculosis infection were downloaded. The two external validation GEO datasets were exploited for subsequent verification of the ferroptosis-related DEGs. We further evaluated the correlation among the ferroptosis-related DEGs, therapeutic effects, and drug resistance. Finally, we tried to reveal the engagement of the ferroptosis-related DEGs in bone destruction during TB infection. The present study identified SOCS1 as the only ferroptosis-related DEGs. Compared to the non-TB patients, up-regulation of SOCS1 was evident in the TB patients. After receiving standard anti-TB treatment, significant down-regulation of SOCS1 confirmed its acceptance as the marker for therapeutic efficacy. The involvement of SOCS1 has also been suggested in the regulation of the micro immune environment in TB. Furthermore, SOCS1 might play an important role in causing bone destruction during TB infection. FRGs-SOCS1 may be the key gene involved in the pathogenesis and progression of TB infection.
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