Increased UBE2L6 regulated by type 1 interferon as potential marker in TB.
Jiao GaoChonghui LiWenjing LiHaotian ChenYu-Rong FuZhengjun YiPublished in: Journal of cellular and molecular medicine (2021)
The aim of this study is to identify potential biomarker of tuberculosis (TB) and determine its function. Differentially expressed mRNAs(DEGs) were selected from a blood database GSE101805, and then, 30 key genes were screened using STING, Cytoscape and further functionally enriched. We then found that only 6 of 13 genes related to ubiquitination (the first in the functional enrichment) were increased significantly. ROC analysis showed that UBE2L6, among 6 genes, had the highest diagnostic value, and then, we found that it also had mild value in differential diagnosis. Moreover, our analysis showed that UBE2L6 may be upregulated by type I interferon, which was further confirmed by us. In addition, we also found that UBE2L6 inhibits the apoptosis of Mycobacterium tuberculosis(Mtb)infected macrophages. Subsequently, we discovered that miR-146a-5p, which may target UBE2L6, is reduced in peripheral blood mononuclear cells (PBMC) and plasma of TB, and it also had certain diagnostic efficiency(AUC=0.791). In brief, we demonstrated that UBE2L6 as well as miR-146a-5p is a potential biomarker for TB and UBE2L6,which may also plays important role in TB by, at least, modulating Mtb-infected macrophage apoptosis.
Keyphrases
- mycobacterium tuberculosis
- pulmonary tuberculosis
- genome wide
- oxidative stress
- endoplasmic reticulum stress
- dendritic cells
- gene expression
- genome wide identification
- genome wide analysis
- signaling pathway
- dna methylation
- risk assessment
- climate change
- hepatitis c virus
- transcription factor
- adverse drug
- human health
- immune response
- data analysis