Evidence map›Paper›PMID 27924063›Full record

ReviewOncotarget2017

ΔNp63α and microRNAs: leveraging the epithelial-mesenchymal transition.

Andrew J Stacy, Michael P Craig, Suraj Sakaram, Madhavi Kadakia

Abstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Molecular Mechanisms of p63-Mediated Squamous Cancer Pathogenesis.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. STAT3, stem cells, cancer stem cells and p63.Cellular & molecular biology letters · 2018
    Review
  16. Review
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.

Andrew J StacyDepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USA.
Michael P CraigDepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USA.
Suraj SakaramDepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USA.
Madhavi KadakiaDepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USA.

Funding

Role of DeltaNp63alpha in Vitamin D Mediated Cell Survival in Skin CancerR01CA154715 · NCI · WRIGHT STATE UNIVERSITY · PI KADAKIA, MADHAVI P · 2012 to 2016
$1.4M
NCI NIH HHS R01 CA154715
6 · The paper itself

Abstract

The epithelial-mesenchymal transition (EMT) is a cellular reprogramming mechanism that is an underlying cause of cancer metastasis. Recent investigations have uncovered an intricate network of regulation involving the TGFβ, Wnt, and Notch signaling pathways and small regulatory RNA species called microRNAs (miRNAs). The activity of a transcription factor vital to the maintenance of epithelial stemness, ΔNp63α, has been shown to modulate the activity of these EMT pathways to either repress or promote EMT. Furthermore, ΔNp63α is a known regulator of miRNA, including those directly involved in EMT. This review discusses the evidence of ΔNp63α as a master regulator of EMT components and miRNA, highlighting the need for a deeper understanding of its role in EMT. This expanded knowledge may provide a basis for new developments in the diagnosis and treatment of metastatic cancer.

Indexed as

AnimalsCell Transformation, NeoplasticCellular ReprogrammingEpithelial-Mesenchymal TransitionGene Expression RegulationHumansMicroRNAsSignal TransductionTranscription FactorsTumor Suppressor ProteinsMicroRNAsTP63 protein, humanTranscription FactorsTumor Suppressor ProteinsbiomarkerEMTmiRNAp63signaling

Identifiers

PMID27924063
PMCPMC5356785

What OpenQuestion holds

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LicenceCC BY
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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.