Comprehensive analysis of aberrantly expressed profiles of mRNA and its relationship with serum galactose-deficient IgA1 level in IgA nephropathy
Adult
Male
0301 basic medicine
Galactose-deficient IgA1
03 medical and health sciences
RNA-deep sequencing
Humans
RNA, Messenger
Differential gene expression
Research
Gene Expression Profiling
R
PTEN Phosphohydrolase
Galactose
Reproducibility of Results
Glomerulonephritis, IGA
IgA nephropathy
Immunoglobulin A
3. Good health
Gene Ontology
Gene Expression Regulation
Case-Control Studies
mRNA microarray
Medicine
Female
DOI:
10.1186/s12967-019-2064-3
Publication Date:
2019-09-23T13:02:42Z
AUTHORS (5)
ABSTRACT
Abstract Background Immunoglobulin A nephropathy (IgAN) is the leading cause of end-stage kidney disease. Previous mRNA microarray profiling studies IgAN revealed inconsistent data. We sought to identify aberrantly expressed genes and biological pathways by integrating gene expression datasets in blood cells performing systematically experimental validation. also explored relationship between target galactose-deficient IgA1 (Gd-IgA1) IgAN. Methods retrieved Gene Expression Omnibus (GEO) Ontology (GO) enrichment Kyoto Encyclopedia Genes Genomes (KEGG) analyses were used for functional analysis. Deep sequencing on RNA isolated from B was The expressions Gd-IgA1 levels serum studied. Results Three with met our inclusion criteria. identified 655 dyregulated genes, including 319 up-regulated 336 down-regulated three GEO a total 35 patients 19 healthy controls. Based process GO term, these are mainly related pentose-phosphate shunt, non-oxidative branch, post-embryonic camera-type eye development leukocyte activation. KEGG pathway analysis data that enriched human T-cell leukemia virus 1 infection, proteoglycans cancer, intestinal immune network IgA production autophagy. further performed deep mRNAs an independent set five persons same clinical demographic characteristics. Seventy-seven overlapped differentially regulated mentioned above, 43 thirty-four genes. next investigated whether correlated patients. Pearson correlation showed PTEN (phosphatase tensin homolog) most powerful negatively levels. Conclusions These results demonstrated autophagy process, might be involved mechanism production.
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