Evidence map›Paper›PMID 27099200›Full record

ArticleJournal of cellular and molecular medicine2016

MicroRNA-224 regulates self-renewal of mouse spermatogonial stem cells via targeting DMRT1.

Na Cui, Guimin Hao, Zhiming Zhao, Feng Wang, Jinfeng Cao, Aimin Yang

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  11. Review
  12. Review
  13. Regulation of mammalian spermatogenesis by miRNAs.Seminars in cell & developmental biology · 2022
    Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. MicroRNA-449b-5p Suppresses Proliferation, Migration, and Invasion of Osteosarcoma by Targeting c-Met.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Na CuiDepartment of Reproduction, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Guimin HaoDepartment of Reproduction, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Zhiming ZhaoDepartment of Reproduction, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Feng WangDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Jinfeng CaoDepartment of Reproduction, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Aimin YangDepartment of Reproduction, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Hebei Medical University · CNSecond Hospital of Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRs) play a key role in the control of gene expression in a wide array of tissue systems, where their functions include the regulation of self-renewal, cellular differentiation, proliferation and apoptosis. However, the function and mechanisms of individual miRs in regulating spermatogonial stem cell (SSC) homeostasis remain unclear. In the present study, we report for the first time that miR-224 is highly expressed in mouse SSCs. Functional assays using miRNA mimics and inhibitors reveal that miR-224 is essential for differentiation of SSCs. Mechanistically, miR-224 promotes differentiation of SSCs via targeting doublesex and Mab-3-related transcription factor 1 (DMRT1). Moreover, WNT/β-catenin signalling pathway is involved in miR-224-mediated regulation of SSCs self-renewal. We further demonstrate that miR-224 overexpression increases the expression of GFRα1 and PLZF, accompanied by the down-regulation of DMRT1 in mouse testes. Our findings provide novel insights into molecular mechanisms regulating differentiation of SSCs and may have important implications for regulating male reproduction.

Indexed as

3' Untranslated RegionsAnimalsBase SequenceBiomarkersCell DifferentiationCell Self RenewalGene Expression RegulationGlial Cell Line-Derived Neurotrophic Factor ReceptorsKruppel-Like Transcription FactorsMaleMice, Inbred BALB CMicroRNAsPromyelocytic Leukemia Zinc Finger ProteinSpermatogoniaStem CellsSubcellular Fractions3' Untranslated RegionsBiomarkersDMRT1 proteinGfra1 protein, mouseGlial Cell Line-Derived Neurotrophic Factor ReceptorsKruppel-Like Transcription FactorsMicroRNAsMIRN224 microRNA, mousePromyelocytic Leukemia Zinc Finger ProteinTranscription FactorsZbtb16 protein, mousedifferentiationDMRT1miR-224reproductionspermatogonial stem cells

Identifiers

PMID27099200
PMCPMC4956939
OpenAlexW2340511426

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.