Evidence map›Paper›PMID 30455250›Full record

ArticleMolecular and cellular biology2019

A Novel Regulatory Axis, CHD1L-MicroRNA 486-Matrix Metalloproteinase 2, Controls Spermatogonial Stem Cell Properties.

Shan-Shan Liu, Eithne Margaret Maguire, Yin-Shan Bai, Li Huang, Yurong Liu, Liping Xu, Iliana Fauzi, Shou-Quan Zhang, Qingzhong Xiao, Ning-Fang Ma

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. CHD1L in cancer and beyond: structure, oncogenic functions, and therapeutic potential.Journal of experimental & clinical cancer research : CR · 2025
    Review
  4. Small RNAs, spermatogenesis, and male infertility: a decade of retrospect.Reproductive biology and endocrinology : RB&E · 2023
    Review
  5. Observational
  6. Regulation of mammalian spermatogenesis by miRNAs.Seminars in cell & developmental biology · 2022
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. MiRNAs Expression Profiling of Bovine (International journal of molecular sciences · 2020
    Article
  13. Uncovering the Physiological Mechanisms Underlying the Roe Deer (Animals : an open access journal from MDPI · 2020
    Article
  14. Article
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

10 authors at 4 institutions in 2 countries.

Shan-Shan LiuAffiliated Cancer Hospital & Institute of Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou, Guangdong, China.
Eithne Margaret MaguireCentre for Clinical Pharmacology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Yin-Shan BaiNational Engineering Research Center for Breeding Swine Industry, Guangdong Provincial Key Laboratory of Agro-Animal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou, Guangdong, China.
Li HuangLaboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou, Guangdong, China.
Yurong LiuAffiliated Cancer Hospital & Institute of Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou, Guangdong, China.
Liping XuLaboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou, Guangdong, China.
Iliana FauziCentre for Clinical Pharmacology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Shou-Quan ZhangNational Engineering Research Center for Breeding Swine Industry, Guangdong Provincial Key Laboratory of Agro-Animal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou, Guangdong, China.
Qingzhong XiaoLaboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou, Guangdong, China q.xiao@qmul.ac.uk nfma@gzhmu.edu.cn.
Ning-Fang MaAffiliated Cancer Hospital & Institute of Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou, Guangdong, China q.xiao@qmul.ac.uk nfma@gzhmu.edu.cn.
Guangzhou Medical University · CNSouth China Agricultural University · CNWilliam Harvey Research Institute · GBQueen Mary University of London · GB

Funding

British Heart Foundation FS/09/044/28007British Heart Foundation PG/11/40/28891British Heart Foundation PG/13/45/30326British Heart Foundation PG/15/11/31279British Heart Foundation PG/15/86/31723British Heart Foundation PG/16/1/31892
6 · The paper itself

Abstract

Spermatogonial stem cells (SSCs) are unipotent germ cells that are at the foundation of spermatogenesis and male fertility. However, the underlying molecular mechanisms governing SSC stemness and growth properties remain elusive. We have recently identified chromodomain helicase/ATPase DNA binding protein 1-like (Chd1l) as a novel regulator for SSC survival and self-renewal, but how these functions are controlled by Chd1l remains to be resolved. Here, we applied high-throughput small RNA sequencing to uncover the microRNA (miRNA) expression profiles controlled by Chd1l and showed that the expression levels of 124 miRNA transcripts were differentially regulated by Chd1l in SSCs. KEGG pathway analysis shows that the miRNAs that are differentially expressed upon Chd1l repression are significantly enriched in the pathways associated with stem cell pluripotency and proliferation. As a proof of concept, we demonstrate that one of the most highly upregulated miRNAs, miR-486, controls SSC stemness gene expression and growth properties. The matrix metalloproteinase 2 (MMP2) gene has been identified as a novel miR-486 target gene in the context of SSC stemness gene regulation and growth properties. Data from cotransfection experiments showed that Chd1l, miR-486, and MMP2 work in concert in regulating SSC stemness gene expression and growth properties. Finally, our data also revealed that MMP2 regulates SSC stemness gene expression and growth properties through activating β-catenin signaling by cleaving N-cadherin and increasing β-catenin nuclear translocation. Our data demonstrate that Chd1l-miR-486-MMP2 is a novel regulatory axis governing SSC stemness gene expression and growth properties, offering a novel therapeutic opportunity for treating male infertility.

Indexed as

Adult Germline Stem CellsAnimalsCell ProliferationCells, CulturedDNA-Binding ProteinsDNA HelicasesMaleMatrix Metalloproteinase 2MiceMicroRNAsPluripotent Stem CellsSpermatogenesisSpermatogoniaTestisTranscription FactorsChd1l protein, mouseDNA-Binding ProteinsDNA HelicasesMatrix Metalloproteinase 2MicroRNAsMIRN486 microRNA, mouseMmp2 protein, mouseTranscription Factorscell apoptosiscell cyclecell proliferationCHD1LmicroRNAsmiR-486MMP2spermatogonial stem cellstemness

Identifiers

PMID30455250
PMCPMC6362313
OpenAlexW2901976286

What OpenQuestion holds

Textmetadata
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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.