Evidence map›Paper›PMID 26815535›Full record

ArticlePloS one2016

MycN Is Critical for the Maintenance of Human Embryonic Stem Cell-Derived Neural Crest Stem Cells.

Jie Ting Zhang, Zhi Hui Weng, Kam Sze Tsang, Lai Ling Tsang, Hsiao Chang Chan, Xiao Hua Jiang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Epigenetic crosstalk in neuroblastoma development and progression.Frontiers in cell and developmental biology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. FOXR2 Stabilizes MYCN Protein and Identifies Non-Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. 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.

Jie Ting ZhangKey Laboratory for Regenerative Medicine, Ministry of Education, Epithelial Cell Biology Research Center, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, PR China.
Zhi Hui WengKey Laboratory for Regenerative Medicine, Ministry of Education, Epithelial Cell Biology Research Center, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, PR China.
Kam Sze TsangDepartment of Anatomical and Cellular Pathology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, PR China.
Lai Ling TsangKey Laboratory for Regenerative Medicine, Ministry of Education, Epithelial Cell Biology Research Center, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, PR China.
Hsiao Chang ChanKey Laboratory for Regenerative Medicine, Ministry of Education, Epithelial Cell Biology Research Center, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, PR China.
Xiao Hua JiangKey Laboratory for Regenerative Medicine, Ministry of Education, Epithelial Cell Biology Research Center, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, PR China.
Chinese University of Hong Kong · CNChinese University of Hong Kong, Shenzhen · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biologic studies of human neural crest stem cells (hNCSCs) are extremely challenging due to the limited source of hNCSCs as well as ethical and technical issues surrounding isolation of early human embryonic tissues. On the other hand, vast majority of studies on MycN have been conducted in human tumor cells, thus, the role of MycN in normal human neural crest development is completely unknown. In the present study, we determined the role of MycN in hNCSCs isolated from in vitro-differentiating human embryonic stem cells (hESCs). For the first time, we show that suppression of MycN in hNCSCs inhibits cell growth and cell cycle progression. Knockdown of MycN in hNCSCs increases the expression of Cdkn1a, Cdkn2a and Cdkn2b, which encodes the cyclin-dependent kinases p21CIP1, p16 INK4a and p15INK4b. In addition, MycN is involved in the regulation of human sympathetic neurogenesis, as knockdown of MycN enhances the expression of key transcription factors involved in sympathetic neuron differentiation, including Phox2a, Phox2b, Mash1, Hand2 and Gata3. We propose that unlimited source of hNCSCs provides an invaluable platform for the studies of human neural crest development and diseases.

Indexed as

Cell ProliferationNeurogenesisCell CycleCell LineCells, CulturedGene Expression Regulation, DevelopmentalGene Knockdown TechniquesHuman Embryonic Stem CellsHumansNeural CrestNeural Stem CellsN-Myc Proto-Oncogene ProteinNuclear ProteinsOncogene ProteinsMYCN protein, humanN-Myc Proto-Oncogene ProteinNuclear ProteinsOncogene Proteins

Identifiers

PMID26815535
PMCPMC4729679
OpenAlexW2403611489

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.