Evidence map›Paper›PMID 35124761›Full record

ArticleInternational urology and nephrology2022

In silico analysis of microRNA genes in azoospermia factor Y-chromosome microdeletions.

Sercan Ergun, Sezgin Gunes, Neslihan Hekim, Sandro C Esteves

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Article in International urology and nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 3 countries.

Sercan ErgunDepartment of Medical Biology, Faculty of Medicine, Ondokuz Mayis University, 55139, Samsun, Turkey.ORCID http://orcid.org/0000-0002-6733-9848
Sezgin GunesDepartment of Medical Biology, Faculty of Medicine, Ondokuz Mayis University, 55139, Samsun, Turkey. sgunes@omu.edu.tr.ORCID http://orcid.org/0000-0002-3103-6482
Neslihan HekimDepartment of Medical Biology, Faculty of Medicine, Ondokuz Mayis University, 55139, Samsun, Turkey.ORCID http://orcid.org/0000-0002-8470-2848
Sandro C EstevesANDROFERT, Andrology and Human Reproduction Clinic, Campinas, SP, Brazil.ORCID http://orcid.org/0000-0002-1313-9680
Ondokuz Mayıs University · TRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMicrodeletion on Y-chromosome is a well-known genetic cause of infertility in azoospermic and oligozoospermic men. RNA transcripts possess microRNA (miRNA) response elements (MRE) that may interact with competing endogenous RNAs (ceRNA), thus repressing their activity. MiRNAs originally targeting transcripts of genes deleted in the Y-chromosome azoospermia factor (AZF) region are expected to be oriented to binding sites of new targets. We investigated miRNAs targeting genes of each AZF locus (AZFa, AZFb, AZFb-c, and AZFc) to determine their corresponding ceRNA using in silico analysis.

methodsThe miRNAs targeting most of the genes deleted in each AZF locus were identified using the miRWalk database. Twelve miRNAs exhibiting potential ceRNA activity were identified and analyzed using the ComiR database. Detected ceRNAs for each AZF locus were processed in the GeneMANIA database for interaction prediction, and the most probably interacted genes were identified.

resultsRPPA2, TMED3, STX7 and ATRX, GOGLB1, KMT2C genes were found potential ceRNAs for the AZFa and AZFb regions, respectively. Furthermore, CNB5, KCNC4, NDUFS1 and TROBP, HEMK1, and ORAI2 genes were the potential ceRNAs for the partially AZFb-c-overlapped region and AZFc regions, respectively.

conclusionOur findings suggest that AZF loci deletion may change post-transcriptional regulation of gene expression through miRNA competition.

Indexed as

AzoospermiaInfertility, MaleMicroRNAsOligospermiaSex Chromosome Disorders of Sex DevelopmentChromosome DeletionChromosomes, Human, YHumansMaleSex Chromosome AberrationsVesicular Transport ProteinsMicroRNAsTMED3 protein, humanVesicular Transport ProteinsAzoospermiaceRNAsInfertilitymiRNAsOligozoospermiaY-chromosome microdeletion

Identifiers

PMID35124761
OpenAlexW4210811929

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.