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. 2018 Aug 13;16(1):78.
doi: 10.1186/s12958-018-0393-3.

Altered miRNA profile in testis of post-cryptorchidopexy patients with non-obstructive azoospermia

Affiliations

Altered miRNA profile in testis of post-cryptorchidopexy patients with non-obstructive azoospermia

Dongdong Tang et al. Reprod Biol Endocrinol. .

Abstract

Background: Cryptorchidism is one of the most common causes of non-obstructive azoospermia (NOA) leading to male infertility. Despite various medical approaches been utilised, many patients still suffer from infertility. MicroRNAs (miRNAs) play vital roles in the progress of spermatogenesis; however, little is known about the miRNA expression profile in the testes. Therefore, the miRNA profile was assessed in the testis of post-cryptorchidopexy patients.

Methods: Three post-cryptorchidopexy testicular tissue samples from patients aged 23, 26 and 28 years old and three testis tissues from patients with obstructive azoospermia (controls) aged 24, 25 and 36 years old were used in this study. Next-generation sequencing (NGS) was used to perform the miRNA expression profiling. Quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) assays were subsequently used to confirm the results of several randomly-selected and annotated miRNAs.

Results: A series of miRNAs were found to be altered between post-cryptorchidopexy testicular tissues and control tissues, including 297 downregulated and 152 upregulated miRNAs. In the subsequent qRT-PCR assays, the expression levels of most of the selected miRNAs (9/12, P < 0.05) were consistent with the results of NGS technology. Furthermore, signal transduction, adaptive immune response and biological regulation were associated with the putative target genes of the differentially-expressed miRNAs via GO analysis. In addition, oxidative phosphorylation, Parkinson's disease and ribosomal pathways were shown to be enriched using KEGG pathway analysis of the differentially-expressed genes.

Conclusions: This study provides a global view of the miRNAs involved in post-cryptorchidopexy testicular tissues as well as the altered expression of miRNAs compared to control tissues, thus confirming the vital role of miRNAs in cryptorchidism.

Keywords: Cryptorchidism; Cryptorchidopexy; Next-generation small RNA sequencing; Spermatogenesis; miRNA.

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Conflict of interest statement

Written informed consent was obtained from all patients and this study was approved by the Ethics Review Board of The First Affiliated Hospital of Anhui Medical University.

Not applicable.

The authors declare that they have no competing interests.

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
HE-staining of cryptorchid tissue and control tissue, which clarify the histopathological characteristics of cryptorchid tissues (a) and control tissues (b).
Fig. 2
Fig. 2
Results of geneome mapping and distribution of RNAs among different categories.
Fig. 3
Fig. 3
The overview of the volcano plot generated by miRNAs profile in cryptorchid tissues and control tissues.
Fig. 4
Fig. 4
Confirmation of differentially expressed miRNAs between cryptorchid tissues and control tissues obtained by NGS using qRT-PCR. (* P <0.05)

References

    1. Matzuk MM, Lamb DJ. Genetic dissection of mammalian fertility pathways. Nat Cell Biol. 2002;4(Suppl):s41–s49. - PubMed
    1. Practice Committee of the American Society for Reproductive Medicine Diagnostic evaluation of the infertile male: a committee opinion. Fertil Steril. 2015;103:e18–e25. - PubMed
    1. Kolon TF, Herndon CD, Baker LA, Baskin LS, Baxter CG, Cheng EY, et al. Evaluation and treatment of cryptorchidism: AUA guideline. J Urol. 2014;192:337–345. doi: 10.1016/j.juro.2014.05.005. - DOI - PubMed
    1. Barthold JS, Gonzalez R. The epidemiology of congenital cryptorchidism, testicular ascent and orchiopexy. J Urol. 2003;170:2396–2401. doi: 10.1097/01.ju.0000095793.04232.d8. - DOI - PubMed
    1. Bao J, Li D, Wang L, Wu J, Hu Y, Wang Z, et al. MicroRNA-449 and microRNA-34b/c function redundantly in murine testes by targeting E2F transcription factor-retinoblastoma protein (E2F-pRb) pathway. J Biol Chem. 2012;287:21686–21698. doi: 10.1074/jbc.M111.328054. - DOI - PMC - PubMed

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