Evidence map›Paper›PMID 25938342›Full record

ArticleThe Journal of investigative dermatology2015

Protein Tyrosine Kinase 6 Regulates UVB-Induced Signaling and Tumorigenesis in Mouse Skin.

Michael I Chastkofsky, Wenjun Bie, Susan M Ball-Kell, Yu-Ying He, Angela L Tyner

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of investigative dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Bioinformatics-based prognostic value andFrontiers in oncology · 2025
    Article
  3. Article
  4. Article
  5. Construction of a Secondary Enclosure for UVB Irradiation of Mice.JID innovations : skin science from molecules to population health · 2023
    Article
  6. Article
  7. Targeting protein tyrosine kinase 6 in cancer.Biochimica et biophysica acta. Reviews on cancer · 2020
    Review
  8. Review
  9. Article
  10. Article
  11. 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

5 authors at 2 institutions in 1 country.

Michael I ChastkofskyDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA; Department of Oral Sciences, College of Dentistry, University of Illinois at Chicago, Chicago, Illinois, USA.
Wenjun BieDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Susan M Ball-KellGlobal Path Imaging and Consulting, Metamora, Illinois, USA.
Yu-Ying HeSection of Dermatology, Department of Medicine, University of Chicago, Chicago, Illinois, USA.
Angela L TynerDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA. Electronic address: atyner@uic.edu.
University of Illinois Chicago · USUniversity of Chicago · US

Funding

ISOLATION OF GENETIC MARKERS FOR INTESTINAL CRYPT CELLSR01DK044525 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TYNER, ANGELA L · 1993 to 2016
$4.8M
Multidisciplinary Oral Science TrainingT32DE018381 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI COOPER, LYNDON F · 2008 to 2019
$3.6M
ISOLATION OF GENETIC MARKERS FOR INTESTINAL CRYPT CELLSR55DK044525 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TYNER, ANGELA L · 1992 to 1992
–
NIDCR NIH HHS 5-T32-DE-18381-4NIDCR NIH HHS T32 DE018381NIDDK NIH HHS DK44525NIDDK NIH HHS R01 DK044525
6 · The paper itself

Abstract

Protein tyrosine kinase 6 (PTK6, also called BRK) is an intracellular tyrosine kinase expressed in the epithelial linings of the gastrointestinal tract and the skin, where it is expressed in nondividing differentiated cells. We found that PTK6 expression increases in the epidermis following UVB treatment. To evaluate the roles of PTK6 in the skin following UVB-induced damage, we exposed back skin of Ptk6 +/+ and Ptk6 -/- SENCAR mice to incremental doses of UVB for 30 weeks. Wild-type mice were more sensitive to UVB and exhibited increased inflammation and greater activation of signal transducer and activator of transcription-3 (STAT3) than Ptk6-/- mice. Disruption of Ptk6 did not have an impact on proliferation, although PTK6 was expressed and activated in basal epithelial cells in wild-type mice following UVB treatment. However, wild-type mice exhibited shortened tumor latency and increased tumor load compared with Ptk6-/- mice, and STAT3 activation was increased in these tumors. PTK6 activation was detected in UVB-induced tumors, and this correlated with increased activating phosphorylation of focal adhesion kinase (FAK) and breast cancer anti-estrogen resistance 1 (BCAR1). Activation of PTK6 was also detected in human squamous cell carcinomas of the skin. Although PTK6 has roles in normal differentiation, it also contributes to UVB-induced injury and tumorigenesis in vivo.

Indexed as

AnimalsApoptosisBiopsy, NeedleCarcinogenesisCarcinoma, Squamous CellCell ProliferationCells, CulturedCell Transformation, NeoplasticDisease Models, AnimalGene Expression RegulationHumansImmunohistochemistryMaleMiceMice, Inbred C57BLMice, Inbred SENCARProtein-Tyrosine KinasesPtk6 protein, mouse

Identifiers

PMID25938342
PMCPMC4567952
OpenAlexW2041927438

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.