Abstract
Background: Genes have an important role in spermatogenesis and the maintenance of fertility, and may act as a potential biomarker for the clinical diagnosis of infertility. However, a comprehensive understanding of how these biological processes of infertility are regulated at the molecular level remains to be illustrated. Methods: In the present study, we sought to identify associated genes by reanalyzing separate studies from GEO datasets (GSE45885, GSE45887, and GSE9210) and validation dataset (GSE4797). DEGs were used the limma package. GO and KEGG pathway enrichment analyses were performed using the clusterprofier package. The STRING database was used construct a protein-protein interaction network. The interaction between mRNA and TF was predicted by using miRWalk. At last, the expression levels of hub genes were determined by TCGA data in GEPIA. Results: The results showed that several shared genes significantly associated with azoospermia. Finally, we effectively screen out two genes (KIF2C and TEKT2) for validation by GSE4797 in spermatozoa of infertile men with Johnsen score. Among these two genes, KIF2C and TEKT2 significantly down-regulated in spermatozoa of infertile men. The regulatory network of TF‐miRNA‐target gene was established, we found KIF2C-miRNAs(has-miR-3154,6075,6760-5p,1251-5p,186-sp)-TFs(EP300,SP1) might work in spermatozoa of infertile men.Conclusions: Our study might help to improve our understanding of the mechanisms in azoospermia and provide diagnostic biomarkers and therapeutics targets.