Evidence map›Paper›PMID 23836497›Full record

ArticleStem cells (Dayton, Ohio)2013

MiRNA-20 and mirna-106a regulate spermatogonial stem cell renewal at the post-transcriptional level via targeting STAT3 and Ccnd1.

Zuping He, Jiji Jiang, Maria Kokkinaki, Lin Tang, Wenxian Zeng, Ian Gallicano, Ina Dobrinski, Martin Dym

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

75 citing papers in PubMed, 170 citations in OpenAlex.

  1. Trial
  2. Unravelling male infertility through epigenetics: present understanding and future challenges.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. The Biology and Regulation of Spermatogonial Stem Cells in the Niche.Advances in experimental medicine and biology · 2025
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Small RNAs, spermatogenesis, and male infertility: a decade of retrospect.Reproductive biology and endocrinology : RB&E · 2023
    Review
  14. Overview of miR-106a Regulatory Roles: from Cancer to Aging.Bioengineering (Basel, Switzerland) · 2023
    Review
  15. Review
  16. Frontiers in cell and developmental biology · 2023
    Review
  17. Article
  18. Life (Basel, Switzerland) · 2022
    Article
  19. Article
  20. Article

15 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 3 countries.

Zuping HeDepartment of Biochemistry and Molecular & Cellular Biology, Georgetown University Medical Center, Washington, USA; Clinical Stem Cell Research Center, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Jiji Jiang
Maria Kokkinaki
Lin Tang
Wenxian Zeng
Ian Gallicano
Ina Dobrinski
Martin Dym
Georgetown University Medical Center · USGeorgetown University · USUniversity of Calgary · CA

Funding

FATE OF SPERMATOGONIAL STEM CELLSR01HD033728 · NICHD · GEORGETOWN UNIVERSITY · PI DYM, MARTIN · 1997 to 2007
$2.6M
NICHD NIH HHS R01 HD033728NICHD NIH HHS R01 HD33728
6 · The paper itself

Abstract

Studies on spermatogonial stem cells (SSCs) are of unusual significance because they are the unique stem cells that transmit genetic information to subsequent generations and they can acquire pluripotency to become embryonic stem-like cells that have therapeutic applications in human diseases. MicroRNAs (miRNAs) have recently emerged as critical endogenous regulators in mammalian cells. However, the function and mechanisms of individual miRNAs in regulating SSC fate remain unknown. Here, we report for the first time that miRNA-20 and miRNA-106a are preferentially expressed in mouse SSCs. Functional assays in vitro and in vivo using miRNA mimics and inhibitors reveal that miRNA-20 and miRNA-106a are essential for renewal of SSCs. We further demonstrate that these two miRNAs promote renewal at the post-transcriptional level via targeting STAT3 and Ccnd1 and that knockdown of STAT3, Fos, and Ccnd1 results in renewal of SSCs. This study thus provides novel insights into molecular mechanisms regulating renewal and differentiation of SSCs and may have important implications for regulating male reproduction.

Indexed as

RNA InterferenceAdult Stem CellsAnimalsBase SequenceCell ProliferationCells, CulturedCyclin D1FemaleGene ExpressionKruppel-Like Transcription FactorsMaleMiceMice, Inbred BALB CMicroRNAsMultigene FamilyPhenotypeCcnd1 protein, mouseCyclin D1Kruppel-Like Transcription FactorsMicroRNAsMirn106 microRNA, mouseMirn20 microRNA, mouseProliferating Cell Nuclear AntigenPromyelocytic Leukemia Zinc Finger ProteinStat3 protein, mouseSTAT3 Transcription FactorZbtb16 protein, mouseCcnd1miRNA-106amiRNA-20Self-renewalSpermatogonial stem cellsSTAT3

Identifiers

PMID23836497
PMCPMC3859454
OpenAlexW1843736399

What OpenQuestion holds

Textmetadata
LicenceTDM
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.