Identification and Analysis of Autophagy-Related Genes as Diagnostic Markers and Potential Therapeutic Targets for Tuberculosis Through Bioinformatics

Author:

Luo Tingting1,Shen Shijie1,Sun Yufei1,El-Ashram Saeed2,Zhang Xia1,Liu Keyu1,Deng Siqi1,Cao Chengzhang1,Alajmi Reem Atalla3,Wu Jiangdong1,Zhang Wanjiang1

Affiliation:

1. Shihezi University

2. Kafrelsheikh University

3. King Saud University

Abstract

Abstract

Background: According to the World Health Organization, Mycobacterium tuberculosis (Mtb) infections affect approximately 25% of the world's population. There is mounting evidence linking autophagy and immunological dysregulation to TB, according to many research. As a result, this research set out to discover TB-related autophagy-related biomarkers, gene regulatory networks, and prospective treatment targets. Methods: We used five autophagy databases to get genes linked to autophagy and GEO databases to get genes connected to TB. Then, functional modules associated with autophagy were obtained by analyzing them using weighted gene coexpression network analysis (WGCNA). Both GO and KEGG were used to examine the ATGs of important modules. Limma, an R tool, was used to identify differentially expressed ATGs, and the external datasets of GSE19435 were used to further confirm their identification. We used DE-ATGs and a protein-protein interaction (PPI) network to search the hub genes. CIBERSORT was used to estimate the kinds and amounts of immune cells. After that, we built a drug-gene interaction network and a network that included messenger RNA, small RNA, DNA, and ceRNA. At last, the differential expression of hub ATGs was confirmed by RT-qPCR, Immunohistochemistry (IHC), and Western blotting (WB). The diagnostic usefulness of hub ATGs was evaluated using receiver operating characteristic (ROC) curve analysis. Results: Including 508 ATGs, four of the nine modules strongly linked with TB were deemed essential. Three hub genes—IL1B, CAPS1, and STAT1—were identified by intersection out of twenty-two DE-ATGs discovered by differential expression analysis. Research into immune cell infiltration found that TB patients had an increased proportion of plasma cells, CD8 T cells, and M0 macrophages. A competitive endogenous RNA (ceRNA) network utilized 10 long non-coding RNAs (lncRNAs) and 2 miRNAs. Then, the IL1B-targeted drug CANAKINUMAB was assessed using this network. During bioinformatics analysis, three hub genes—IL1B, CAPS1, and STAT1—were validated using WB/RT-qPCR/IHC in mouse and macrophage infection models. In most cases, the new findings corroborated the old ones. Conclusion: We found that IL1B, CASP1, and STAT1 are important biomarkers for TB. As a result, these crucial hub genes may hold promise as TB treatment targets.

Publisher

Springer Science and Business Media LLC

Reference61 articles.

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