Evidence map›Paper›PMID 31264291›Full record

ReviewMolecular carcinogenesis2019

The role of T-cell protein tyrosine phosphatase in epithelial carcinogenesis.

Liza D Morales, Anna K Archbold, Serena Olivarez, Thomas J Slaga, John DiGiovanni, Dae Joon Kim

Open access · greenAbstract readReview
In one paragraph

Review in Molecular carcinogenesis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Antioxidant and Anti-Inflammatory Effects of CrudeAntioxidants (Basel, Switzerland) · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. PTPN2 in the Immunity and Tumor Immunotherapy: A Concise Review.International journal of molecular sciences · 2022
    Review
  8. T Cell Protein Tyrosine Phosphatase in Glucose Metabolism.Frontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. 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

6 authors at 3 institutions in 1 country.

Liza D MoralesDepartment of Human Genetics, School of Medicine, University of Texas Rio Grande Valley, Edinburg, Texas.
Anna K ArchboldDepartment of Molecular Science, School of Medicine, University of Texas Rio Grande Valley, Edinburg, Texas.
Serena OlivarezDepartment of Molecular Science, School of Medicine, University of Texas Rio Grande Valley, Edinburg, Texas.
Thomas J SlagaDepartment of Pharmacology, School of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
John DiGiovanniDivision of Pharmacology & Toxicology, College of Pharmacy, The University of Texas at Austin, Austin, Texas.ORCID 0000-0003-4233-6728
Dae Joon KimDepartment of Human Genetics, School of Medicine, University of Texas Rio Grande Valley, Edinburg, Texas.ORCID 0000-0002-7977-9955
The University of Texas Rio Grande Valley · USAustin College · USThe University of Texas Health Science Center at San Antonio · US

Funding

The role of TC-PTP in skin carcinogenesisR01ES022250 · NIEHS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI KIM, DAE JOON · 2013 to 2017
$1.7M
NIEHS NIH HHS R01 ES022250
6 · The paper itself

Abstract

T-cell protein tyrosine phosphatase (TC-PTP, encoded by PTPN2) is a nonreceptor PTP that is most highly expressed in hematopoietic tissues. TC-PTP modulates a variety of physiological functions including cell cycle progression, cell survival and proliferation, and hematopoiesis through tyrosine dephosphorylation of its target substrates, such as EGFR, JAK1, JAK3, STAT1, and STAT3. Studies with whole or tissue-specific loss of TC-PTP function transgenic mice have shown that TC-PTP has crucial roles in the regulation of the immune response, insulin signaling, and oncogenic signaling. More recently, the generation of epidermal-specific TC-PTP-deficient mice for use in multistage skin carcinogenesis bioassays demonstrated that TC-PTP suppresses skin tumor formation by negatively regulating STAT3 and AKT signaling. Further investigation showed that TC-PTP also minimizes UVB-induced epidermal cell damage by promoting apoptosis through the negative regulation of Flk-1/JNK signaling. These findings provide major evidence for a tumor suppressive function for TC-PTP against environment-induced skin cancer. Here, we will discuss TC-PTP, its substrates, and its functions with an emphasis on its role in skin carcinogenesis.

Indexed as

AnimalsCarcinogenesisCell CycleCell ProliferationCell SurvivalEpidermisEpithelial CellsHematopoiesisHumansProtein Tyrosine Phosphatase, Non-Receptor Type 2Signal TransductionProtein Tyrosine Phosphatase, Non-Receptor Type 2AKTcarcinogenesisFlk-1STAT3TC-PTP

Identifiers

PMID31264291
PMCPMC6692238
OpenAlexW2955334787

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.