Evidence map›Paper›PMID 7690544›Full record

ArticleThe Biochemical journal1993

Interleukin-2 induces tyrosine phosphorylation of the vav proto-oncogene product in human T cells: lack of requirement for the tyrosine kinase lck.

G A Evans, O M Howard, R Erwin, W L Farrar

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Regulatory and signaling properties of the Vav family.Molecular and cellular biology · 2000
    Review
  9. Article
  10. Review
  11. Genes in the pX region of human T cell leukemia virus I influence Vav phosphorylation in T cells.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  12. p95vav associates with the nuclear protein Ku-70.Molecular and cellular biology · 1996
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Hematopoietic development of vav-/- mouse embryonic stem cells.Proceedings of the National Academy of Sciences of the United States of America · 1994
    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

4 authors at 2 institutions in 1 country.

G A EvansBiological Carcinogenesis and Development Program, Program Resources/DynCorp, Frederick, MD.
O M Howard
R Erwin
W L Farrar
LabCorp (United States) · USFrederick National Laboratory for Cancer Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The haematopoietic protein, p95vav, has been shown to be a tyrosine kinase substrate and to have tyrosine kinase-modulated guanine-nucleotide-releasing-factor activity. This implies a function in the control of ras or ras-like proteins. Because ras activation has been shown to be a downstream event following stimulation of the interleukin-2 (IL-2) receptor, we investigated the possibility that vav was involved in IL-2 signal transduction pathways, using human T cells as a model. We found rapid tyrosine phosphorylation of vav in response to IL-2 within 1 min, with maximum increase of phosphorylation of 5-fold occurring by 5 min after treatment in normal human T cells. IL-2 stimulation of the human T-cell line YT and a subclone of the YT cell line (YTlck-) that does not express message for the src-family kinase p56lck also results in a rapid rate of tyrosine phosphorylation of vav of more than 5-fold by 5 min. These results suggest that vav may play an important role in IL-2-stimulated signal transduction and that there is not a strict requirement for the tyrosine kinase p56lck.

Indexed as

Cell Cycle ProteinsHumansImmunoblottingImmunosorbent TechniquesInterleukin-2Lymphocyte ActivationLymphocyte Specific Protein Tyrosine Kinase p56(lck)LymphomaMutationPhosphotyrosinePhytohemagglutininsProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins c-vavSignal TransductionCell Cycle ProteinsInterleukin-2Lymphocyte Specific Protein Tyrosine Kinase p56(lck)MAS1 protein, humanPhosphotyrosinePhytohemagglutininsProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins c-vavTyrosineVAV1 protein, human

Identifiers

PMID7690544
PMCPMC1134459
OpenAlexW2441853607

What OpenQuestion holds

Textmetadata
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.