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dc.contributor.authorDas, Suchismita
dc.contributor.authorGuha, Pokhraj
dc.contributor.authorNath, Monika
dc.contributor.authorDas, Sandipan
dc.contributor.authorSen, Surojit
dc.contributor.authorSahu, Jagajjit
dc.contributor.authorKopanska, Marta
dc.contributor.authorDutta, Sulagna
dc.contributor.authorJamal, Qazi Mohammad Sajid
dc.contributor.authorKesari, Kavindra Kumar
dc.contributor.authorSengupta, Pallav
dc.contributor.authorSláma, Petr
dc.contributor.authorRoychoudhury, Shubhadeep
dc.date.accessioned2023-09-19T00:03:20Z
dc.date.available2023-09-19T00:03:20Z
dc.date.issued2022
dc.identifier.issn2073-4425 Sherpa/RoMEO, JCR
dc.identifier.urihttps://repozitar.mendelu.cz/xmlui/handle/20.500.12698/1779
dc.description.abstractMale infertility is a global public health concern. Teratozoospermia is a qualitative anomaly of spermatozoa morphology, contributing significantly to male infertility, whereas azoospermia is the complete absence of spermatozoa in the ejaculate. Thus, there is a serious need for unveiling the common origin and/or connection between both of these diseases, if any. This study aims to identify common potential biomarker genes of these two diseases via an in silico approach using a meta-analysis of microarray data. In this study, a differential expression analysis of genes was performed on four publicly available RNA microarray datasets, two each from teratozoospermia (GSE6872 and GSE6967) and azoospermia (GSE145467 and GSE25518). From the analysis, 118 DEGs were found to be common to teratozoospermia and azoospermia, and, interestingly, sperm autoantigenic protein 17 (SPA17) was found to possess the highest fold change value among all the DEGs (9.471), while coiled-coil domain-containing 90B (CCDC90B) and coiled-coil domain-containing 91 (CCDC91) genes were found to be common among three of analyses, i.e., Network Analyst, ExAtlas, and GEO2R. This observation indicates that SPA17, CCDC90B, and CCDC91 genes might have significant roles to play as potential biomarkers for teratozoospermia and azoospermia. Thus, our study opens a new window of research in this area and can provide an important theoretical basis for the diagnosis and treatment of both these diseases.en
dc.format1721
dc.publisherMDPI AG (Multidisciplinary Digital Publishing Institute-MDPI)
dc.relation.ispartofGenes
dc.relation.urihttps://doi.org/10.3390/genes13101721
dc.rightsCC BY 4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectmale infertilityen
dc.subjectteratozoospermiaen
dc.subjectazoospermiaen
dc.subjectbiomarker genesen
dc.subjectSPA17en
dc.subjectCCDC90Ben
dc.subjectCCDC91en
dc.titleA Comparative Cross-Platform Analysis to Identify Potential Biomarker Genes for Evaluation of Teratozoospermia and Azoospermiaen
dc.typeJ_ČLÁNEK
dc.date.updated2023-09-19T00:03:20Z
dc.description.versionOA
local.identifier.doi10.3390/genes13101721
local.identifier.scopus2-s2.0-85140624357
local.identifier.wos000875071700001
local.number10
local.volume13
local.identifier.obd43923466
local.identifier.e-issn2073-4425
dc.identifier.orcidSláma, Petr 0000-0003-0570-259X
local.contributor.affiliationAF


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Except where otherwise noted, this item's license is described as CC BY 4.0