Evidence map›Paper›PMID 24687960›Full record

ArticleThe Journal of experimental medicine2014

Interleukin-7 receptor mutants initiate early T cell precursor leukemia in murine thymocyte progenitors with multipotent potential.

Louise M Treanor, Sheng Zhou, Laura Janke, Michelle L Churchman, Zhijun Ma, Taihe Lu, Shann-Ching Chen, Charles G Mullighan, Brian P Sorrentino

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
12.8field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Review
  3. Transcriptional network dynamics in early T cell development.The Journal of experimental medicine · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Frontiers in cell and developmental biology · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. MutantCancer research · 2021
    Article
  19. Article
  20. Review

6 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 1 institution in 1 country.

Louise M TreanorDepartment of Hematology and 2 Department of Pathology, Division of Experimental Hematology, St. Jude Children's Research Hospital, Memphis, TN 38105.
Sheng Zhou
Laura Janke
Michelle L Churchman
Zhijun Ma
Taihe Lu
Shann-Ching Chen
Charles G Mullighan
Brian P Sorrentino
St. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
VIROSOME/PROTEOLIPOSOME MEDIATED GENE TRANSFERP01HL053749 · NHLBI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEISS, MITCHELL J · 1994 to 2022
$43.6M
NCI NIH HHS P30 CA021765NCI NIH HHS P30 CA 21765NHLBI NIH HHS P01 HL053749NHLBI NIH HHS P01 HL 53749
6 · The paper itself

Abstract

Early T cell precursor acute lymphoblastic leukemia (ETP-ALL) exhibits lymphoid, myeloid, and stem cell features and is associated with a poor prognosis. Whole genome sequencing of human ETP-ALL cases has identified recurrent mutations in signaling, histone modification, and hematopoietic development genes but it remains to be determined which of these abnormalities are sufficient to initiate leukemia. We show that activating mutations in the interleukin-7 receptor identified in human pediatric ETP-ALL cases are sufficient to generate ETP-ALL in mice transplanted with primitive transduced thymocytes from p19(Arf-/-) mice. The cellular mechanism by which these mutant receptors induce ETP-ALL is the block of thymocyte differentiation at the double negative 2 stage at which myeloid lineage and T lymphocyte developmental potential coexist. Analyses of samples from pediatric ETP-ALL cases and our murine ETP-ALL model show uniformly high levels of LMO2 expression, very low to undetectable levels of BCL11B expression, and a relative lack of activating NOTCH1 mutations. We report that pharmacological blockade of Jak-Stat signaling with ruxolitinib has significant antileukemic activity in this ETP-ALL model. This new murine model recapitulates several important cellular and molecular features of ETP-ALL and should be useful to further define novel therapeutic approaches for this aggressive leukemia.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarcinogenesisCell DifferentiationChildDisease Models, AnimalGene Expression Regulation, NeoplasticHumansJanus KinasesLIM Domain ProteinsMiceMultipotent Stem CellsMutationNeoplasm TransplantationNitrilesp38 Mitogen-Activated Protein KinasesAdaptor Proteins, Signal TransducingBcl11b protein, mouseJanus KinasesLIM Domain ProteinsLmo2 protein, mouseNitrilesp38 Mitogen-Activated Protein KinasesPyrazolesPyrimidinesReceptors, Interleukin-7Receptors, NotchRepressor ProteinsRNA, MessengerruxolitinibSTAT Transcription FactorsTumor Suppressor Proteins

Identifiers

PMID24687960
PMCPMC3978278
OpenAlexW2096885745

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.