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pmid:31832523

Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism.

Yu Zhou · Deying Zhang · Bo Liu · Dong Hu · Lianju Shen · Chunlan Long · Yihang Yu · Tao Lin · Xing Liu · Dawei He · Guanghui Wei

Genes & diseases · 2019 doi:10.1016/j.gendis.2018.11.002

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Data

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title
Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism.
doi
10.1016/j.gendis.2018.11.002
pmid
31832523
authors array · 11 items
[0]
Yu Zhou
[1]
Deying Zhang
[2]
Bo Liu
[3]
Dong Hu
[4]
Lianju Shen
[5]
Chunlan Long
[6]
Yihang Yu
[7]
Tao Lin
[8]
Xing Liu
[9]
Dawei He
[10]
Guanghui Wei
journal
Genes & diseases
year
2019
abstract
This study aims to determine key genes and pathways that could play important roles in the spermatogenic process of patients with cryptorchidism. The gene expression profile data of GSE25518 was obtained from the Gene Expression Omnibus (GEO) database. Microarray data were analyzed using BRB-Array Tools to identify differentially expressed genes (DEGs) between high azoospermia risk (HAZR) patients and controls. In addition, other analytical methods were deployed, including hierarchical clustering analysis, class comparison between patients with HAZR and the normal control group, gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and the construction of a protein-protein interaction (PPI) network. In total, 1015 upregulated genes and 1650 downregulated genes were identified. GO and KEGG analysis revealed enrichment in terms of changes in the endoplasmic reticulum cellular component and the endoplasmic reticulum protein synthetic process in the HAZR group. Furthermore, the arachidonic acid pathway and mTOR pathway were also identified as important pathways, while RICTOR and GPX8 were indentified as key genes involved in the spermatogenic process of patients with cryptorchidism. In present study, we found that changes in the synthesis of endoplasmic reticulum proteins, arachidonic acid and the mTOR pathway are important in the incidence and spermatogenic process of cryptorchidism. GPX8 and RICTOR were also identified as key genes associated with cryptorchidism. Collectively, these data may provide novel clues with which to explore the precise etiology and mechanism underlying cryptorchidism and cryptorchidism-induced human infertility.
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Testis developmental gene expression in cryptorchid boys at risk of azoospermia
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The top 30 genes upregulated by a fold-change of >2, a false discovery rate of <0.05 and a P-value of <0.01.
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The top 30 genes downregulated with a fold-change of <0.5, a false discovery rate of <0.05 and a P-value of <0.01.
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Function enrichment results of differentially expressed genes in different biological categories: molecular function, biological processes and cellular components.
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Results derived from the KEGG pathway analysis.
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PMC6889044
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Pathway enrichment analysis of DEGs
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Table 4
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Results derived from the KEGG pathway analysis.
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0.0855002
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section[12]/table-wrap[1]#tbl4
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A t-test was used to compare these two groups and identify DEGS, where P < 0.01.
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The gene expression profile data of GSE25518 (an ID code relating to specific expression data) based on the platform of GPL570 (Affymetrix Human Genome U133 Plus 2.0 Array) were obtained from the Gene Expression Omnibus (GEO) database, National Center for Biotechnology Information (NCBI) (http://www.ncbi.nlm.nih.gov/geo/).
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The paper names GSE25518 in Gene Expression Omnibus (GEO), National Center for Biotechnology Information (NCBI) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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The gene expression profile data of GSE25518 was obtained from the Gene Expression Omnibus (GEO) database. Microarray data were analyzed using BRB-Array Tools to identify differentially expressed genes (DEGs) between high azoospermia risk (HAZR) patients and controls. In addition, other analytical methods were deployed, including hierarchical clustering analysis, class comparison between patients with HAZR and the normal control group, gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and the construction of a protein-protein interaction (PPI) network. In total, 1015 upregulated genes and 1650 downregulated genes were identified. GO and KEGG analysis revealed enrichment in terms of changes in the endoplasmic reticulum cellular component and the endoplasmic reticulum protein synthetic process in the HAZR group. Furthermore, the arachidonic acid pathway and mTOR pathway were also identified as important pathways, while RICTOR and GPX8 were indentified as key genes involved in the spermatogenic process of patients with cryptorchidism. In present study, we found that changes in the synthesis of endoplasmic reticulum proteins, arachidonic acid and the mTOR pathway are important in the incidence and spermatogenic process of cryptorchidism. GPX8 and RICTOR were also identified as key genes associated with cryptorchidism. 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components.", "structure": {"pmcid": "PMC6889044", "section_index": 11, "section_title": "Analysis of GO clustering", "row_count": 14, "column_count": 5}, "table": {"label": "Table 3", "caption": "Function enrichment results of differentially expressed genes in different biological categories: molecular function, biological processes and cellular components.", "rows": [["GO-ID", "Category", "Term", "Count", "P-value"], ["GO:0001822", "BP", "Kidney development", "4", "0.0294136"], ["GO:0051260", "BP", "Protein homo-oligomerization", "5", "0.0477502"], ["GO:0007420", "BP", "Brain development", "5", "0.0566024"], ["GO:0035556", "BP", "Intracellular signal transduction", "7", "0.0904985"], ["GO:0001525", "BP", "Angiogenesis", "8", "0.0017069"], ["GO:0005783", "CC", "Endoplasmic reticulum", "16", "0.0012454"], ["GO:0005789", "CC", "Endoplasmic reticulum membrane", "15", "0.0060193"], ["GO:0005788", "CC", "Endoplasmic reticulum lumen", "6", "0.0166542"], ["GO:0005743", "CC", "Mitochondrial 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