Evidence map›Paper›PMID 29038451›Full record

ArticleScientific reports2017

TC-PTP regulates the IL-7 transcriptional response during murine early T cell development.

K A Pike, T Hatzihristidis, S Bussières-Marmen, F Robert, N Desai, D Miranda-Saavedra, J Pelletier, M L Tremblay

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. PTPN2 in the Immunity and Tumor Immunotherapy: A Concise Review.International journal of molecular sciences · 2022
    Review
  5. T Cell Protein Tyrosine Phosphatase in Glucose Metabolism.Frontiers in cell and developmental biology · 2021
    Review
  6. Interleukin (IL)-7 Signaling in the Tumor Microenvironment.Advances in experimental medicine and biology · 2021
    Article
  7. Review
  8. Protein Tyrosine Phosphatases as Potential Regulators of STAT3 Signaling.International journal of molecular sciences · 2018
    Review
  9. 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

8 authors at 2 institutions in 3 countries.

K A PikeRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada.
T HatzihristidisRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada.
S Bussières-MarmenRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada.
F RobertRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada.
N DesaiRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada.
D Miranda-SaavedraCentro de Biología Molecular Severo Ochoa, CSIC/Universidad Autónoma de Madrid, 28049, Madrid, Spain.
J PelletierRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada.
M L TremblayRosalind and Morris Goodman Cancer Centre, McGill University, Montréal, QC H3A 1A3, Canada. michel.tremblay@mcgill.ca.ORCID 0000-0002-0281-541X
McGill University Health Centre · CAUniversity of Oxford · GB

Funding

CIHR MOP-62887
6 · The paper itself

Abstract

Cytokines play a critical role in directing the discrete and gradual transcriptional changes that define T cell development. The interleukin-7 receptor (IL-7R), via its activation of the JAK-STAT pathway, promotes gene programs that change dynamically as cells progress through T cell differentiation. The molecular mechanism(s) directing differential gene expression downstream of the IL-7R are not fully elucidated. Here, we have identified T cell protein tyrosine phosphatase (TC-PTP), also known as PTPN2, as a negative regulator of IL-7R-STAT signaling in T cell progenitors, contributing to both the quantitative and qualitative nature of STAT-gene targeting. Novel genetic strategies used to modulate TC-PTP expression demonstrate that depletion of TC-PTP expression heightens the phosphorylation of STAT family members, causing aberrant expression of an interferon-response gene profile. Such molecular re-programming results in deregulation of early development checkpoints culminating in inefficient differentiation of CD4

Indexed as

Transcription, GeneticAnimalsBiomarkersCell DifferentiationGene Expression RegulationInflammation MediatorsInterferonsInterleukin-7LymphopoiesisMiceMice, KnockoutProtein Tyrosine Phosphatase, Non-Receptor Type 2RNA InterferenceRNA, Small InterferingSignal TransductionStem CellsBiomarkersInflammation MediatorsInterferonsInterleukin-7Protein Tyrosine Phosphatase, Non-Receptor Type 2Ptpn2 protein, mouseRNA, Small Interfering

Identifiers

PMID29038451
PMCPMC5643372
OpenAlexW2763136388

What OpenQuestion holds

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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.