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

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 T...

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Main Authors: Yu Zhou, Deying Zhang, Bo Liu, Dong Hu, Lianju Shen, Chunlan Long, Yihang Yu, Tao Lin, Xing Liu, Dawei He, Guanghui Wei
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2019-12-01
Series:Genes and Diseases
Online Access:http://www.sciencedirect.com/science/article/pii/S2352304218301326
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author Yu Zhou
Deying Zhang
Bo Liu
Dong Hu
Lianju Shen
Chunlan Long
Yihang Yu
Tao Lin
Xing Liu
Dawei He
Guanghui Wei
author_facet Yu Zhou
Deying Zhang
Bo Liu
Dong Hu
Lianju Shen
Chunlan Long
Yihang Yu
Tao Lin
Xing Liu
Dawei He
Guanghui Wei
author_sort Yu Zhou
collection DOAJ
description 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. Keywords: Arachidonic acid pathway, Bioinformatics, Cryptorchidism, Differentially expressed genes, GPX8, mTOR, RITOR, Spermatogenic
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spelling doaj.art-f373ec2a9e654f40b8845577df5e42522023-09-03T09:36:05ZengKeAi Communications Co., Ltd.Genes and Diseases2352-30422019-12-0164431440Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidismYu Zhou0Deying Zhang1Bo Liu2Dong Hu3Lianju Shen4Chunlan Long5Yihang Yu6Tao Lin7Xing Liu8Dawei He9Guanghui Wei10Department of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; Chongqing Key Laboratory of Pediatrics, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, China; Chongqing Key Laboratory of Pediatrics, China; Corresponding author. Department of Urology, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.Department of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, ChinaChongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, China; Chongqing Key Laboratory of Pediatrics, ChinaChongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, China; Chongqing Key Laboratory of Pediatrics, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, China; Chongqing Key Laboratory of Pediatrics, ChinaDepartment of Urology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China; Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering, China; China International Science and Technology Cooperation Base of Child Development and Critical Disorders, China; Chongqing Key Laboratory of Pediatrics, China; Corresponding author. Department of Urology, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.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. Keywords: Arachidonic acid pathway, Bioinformatics, Cryptorchidism, Differentially expressed genes, GPX8, mTOR, RITOR, Spermatogenichttp://www.sciencedirect.com/science/article/pii/S2352304218301326
spellingShingle Yu Zhou
Deying Zhang
Bo Liu
Dong Hu
Lianju Shen
Chunlan Long
Yihang Yu
Tao Lin
Xing Liu
Dawei He
Guanghui Wei
Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
Genes and Diseases
title Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
title_full Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
title_fullStr Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
title_full_unstemmed Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
title_short Bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
title_sort bioinformatic identification of key genes and molecular pathways in the spermatogenic process of cryptorchidism
url http://www.sciencedirect.com/science/article/pii/S2352304218301326
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