Evidence map›Paper›PMID 25609089›Full record

ArticleMolecular biology of the cell2015

Notch and TGF-β pathways cooperatively regulate receptor protein tyrosine phosphatase-κ (PTPRK) gene expression in human primary keratinocytes.

Yiru Xu, Siliang Xue, Jin Zhou, John J Voorhees, Gary J Fisher

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2015. 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
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Distinct and shared effects of individual γ-secretase inhibitors on human keratinocytes.JID innovations : skin science from molecules to population health · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Protein Tyrosine Phosphatases as Potential Regulators of STAT3 Signaling.International journal of molecular sciences · 2018
    Review
  14. Article
  15. Article
  16. Molecular Pathways: Targeting Protein Tyrosine Phosphatases in Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    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

5 authors at 1 institution in 1 country.

Yiru XuDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109 xuyiru@umich.edu.
Siliang XueDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109.
Jin ZhouDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109.
John J VoorheesDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109.
Gary J FisherDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109.
University of Michigan · US

Funding

Receptor Protein Tyrosine Phosphatase-k Regulation of EGFRR01ES012920 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FISHER, GARY J, XU, YIRU · 2005 to 2015
$3.3M
NIEHS NIH HHS 5R01 ES012920NIEHS NIH HHS R01 ES012920
6 · The paper itself

Abstract

Receptor protein tyrosine phosphatase-κ (PTPRK) specifically and directly dephosphorylates epidermal growth factor receptor (EGFR), thereby limiting EGFR function in primary human keratinocytes. PTPRK expression is increased by the TGF-β/Smad3 pathway and cell-cell contact. Because the Notch receptor pathway is responsive to cell-cell contact and regulates keratinocyte growth and differentiation, we investigated the interplay between Notch and TGF-β pathways in regulation of PTPRK expression in human keratinocytes. Suppression of Notch signaling by γ-secretase inhibitors substantially reduced cell contact induction of PTPRK gene expression. In sparse keratinocyte cultures, addition of soluble Notch-activating ligand jagged one peptide (Jag1) induced PTPRK. Of interest, cell contact-induced expression of TGF-β1 and TGF-β receptor inhibitor SB431542 inhibited contact-induced expression of PTPRK. Furthermore, inhibition of Notch signaling, via knockdown of Notch1 or by γ-secretase inhibitors, significantly reduced TGF-β-induced PTPRK gene expression, indicating that Notch and TGF-β pathways function together to regulate PTPRK. Of importance, the combination of Jag1 plus TGF-β results in greater PTPRK expression and lower EGFR tyrosine phosphorylation than either ligand alone. These data indicate that Notch and TGF-β act in concert to stimulate induction of PTPRK, which suppresses EGFR activation in human keratinocytes.

Indexed as

Cell CommunicationCells, CulturedEnzyme InductionErbB ReceptorsGene ExpressionHumansKeratinocytesPrimary Cell CultureReceptor-Like Protein Tyrosine Phosphatases, Class 2Receptors, NotchSignal TransductionTransforming Growth Factor betaEGFR protein, humanErbB ReceptorsPTPRK protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 2Receptors, NotchTransforming Growth Factor beta

Identifiers

PMID25609089
PMCPMC4357517
OpenAlexW2141393840

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.