Evidence map›Paper›PMID 15452180›Full record

ArticleThe Journal of experimental medicine2004

The loss of PTEN allows TCR alphabeta lineage thymocytes to bypass IL-7 and Pre-TCR-mediated signaling.

Thijs J Hagenbeek, Marianne Naspetti, Fabrice Malergue, Fabien Garçon, Jacques A Nunès, Kitty B J M Cleutjens, Jan Trapman, Paul Krimpenfort, Hergen Spits

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

74 citing papers in PubMed, 119 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Food for thought: Nutrient metabolism controlling early T cell development.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. PTEN in Immunity.Current topics in microbiology and immunology · 2022
    Article
  11. Metabolic regulation of T cell development.Frontiers in immunology · 2022
    Review
  12. Article
  13. Review
  14. PI3K in T Cell Adhesion and Trafficking.Frontiers in immunology · 2021
    Review
  15. Article
  16. PTEN in Regulating Hematopoiesis and Leukemogenesis.Cold Spring Harbor perspectives in medicine · 2020
    Review
  17. Review
  18. The Genetics and Mechanisms of T-Cell Acute Lymphoblastic Leukemia.Cold Spring Harbor perspectives in medicine · 2020
    Review
  19. Review
  20. Review

14 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 2 countries.

Thijs J HagenbeekDepartment of Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Marianne Naspetti
Fabrice Malergue
Fabien Garçon
Jacques A Nunès
Kitty B J M Cleutjens
Jan Trapman
Paul Krimpenfort
Hergen Spits
The Netherlands Cancer Institute · NLAmsterdam UMC Location University of Amsterdam · NLErasmus University Rotterdam · NLInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The phosphatase and tensin homologue deleted on chromosome 10 (PTEN) negatively regulates cell survival and proliferation mediated by phosphoinositol 3 kinases. We have explored the role of the phosphoinositol(3,4,5)P3-phosphatase PTEN in T cell development by analyzing mice with a T cell-specific deletion of PTEN. Pten(flox/flox)Lck-Cre mice developed thymic lymphomas, but before the onset of tumors, they showed normal thymic cellularity. To reveal a regulatory role of PTEN in proliferation of developing T cells we have crossed PTEN-deficient mice with mice deficient for interleukin (IL)-7 receptor and pre-T cell receptor (TCR) signaling. Analysis of mice deficient for Pten and CD3gamma; Pten and gammac; or Pten, gammac, and Rag2 revealed that deletion of PTEN can substitute for both IL-7 and pre-TCR signals. These double- and triple-deficient mice all develop normal levels of CD4CD8 double negative and double positive thymocytes. These data indicate that PTEN is an important regulator of proliferation of developing T cells in the thymus.

Indexed as

AnimalsCell ProliferationCell SurvivalDNA PrimersFlow CytometryGenotypeImmunoblottingImmunoprecipitationInterleukin-7MiceMice, KnockoutPolymerase Chain ReactionProtein Tyrosine PhosphatasesPTEN PhosphohydrolaseReceptors, Antigen, T-Cell, alpha-betaSignal TransductionDNA PrimersInterleukin-7Protein Tyrosine PhosphatasesPTEN PhosphohydrolasePten protein, mouseReceptors, Antigen, T-Cell, alpha-betaTumor Suppressor Proteins

Identifiers

PMID15452180
PMCPMC2213281
OpenAlexW2097910692

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.