Evidence map›Paper›PMID 12955078›Full record

ArticleOncogene2003

Catalytic-dependent and -independent roles of SHP-2 tyrosine phosphatase in interleukin-3 signaling.

Wen-Mei Yu, Teresa S Hawley, Robert G Hawley, Cheng-Kui Qu

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

43 citing papers in PubMed, 69 citations in OpenAlex.

  1. Tyrosine phosphataseFrontiers in immunology · 2024
    Review
  2. Review
  3. A comprehensive review of SHP2 and its role in cancer.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review
  4. Article
  5. Targeting SHP2 phosphatase in hematological malignancies.Expert opinion on therapeutic targets · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Expression and significance of SHP-2 in human papillomavirus infected cervical cancer.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2012
    Article
  20. 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 3 institutions in 1 country.

Wen-Mei YuDepartment of Hematopoiesis, Jerome H Holland Laboratory for the Biomedical Sciences, American Red Cross, 15601 Crabbs Branch Way, Rockville, MD 20855, USA.
Teresa S Hawley
Robert G Hawley
Cheng-Kui Qu
American Red Cross · USGeorge Washington University · USWashington University Medical Center · US

Funding

Tyrosine Phosphatases and Hematopoietic Cell RegulationR01HL068212 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI QU, CHENG-KUI · 2002 to 2012
$3.2M
Embryoid Body-derived Hematopoietic Stem Cell LinesR01HL066305 · NHLBI · GEORGE WASHINGTON UNIVERSITY · PI HAWLEY, ROBERT G. · 2001 to 2005
$1.7M
NHLBI NIH HHS R01HL66305NHLBI NIH HHS R01HL68212
6 · The paper itself

Abstract

SHP-2 tyrosine phosphatase is highly expressed in hematopoietic cells, however, the function of SHP-2 in hematopoietic cell signaling is not well understood. Here we focus on the role of SHP-2 phosphatase in the signal transduction of interleukin (IL)-3, a cytokine involved in hematopoietic cell survival, proliferation, and differentiation. We established immortalized SHP-2(-/-) hematopoietic cell pools and showed that IL-3-induced proliferative response was diminished in SHP-2(-/-) cells. Moreover, inhibition of the catalytic activity of SHP-2 in wild-type (WT) bone marrow hematopoietic progenitor cells and Ba/F3 cells by overexpression of catalytically inactive SHP-2 mutant suppressed their differentiative and proliferative responses to IL-3, demonstrating an important positive role for SHP-2 in IL-3 signal transduction. Further biochemical analyses revealed that IL-3-induced Jak/Stat, Erk, and PI3 kinase pathways in SHP-2(-/-) cells were impaired and reintroduction of WT SHP-2 into mutant cells partially restored IL-3 signaling. Interestingly, in catalytically inactive SHP-2-overexpressing Ba/F3 cells, although IL-3-induced activation of Jak2 and Erk kinases was reduced and shortened, PI3 kinase activation remained unaltered. Taken together, these results suggest that SHP-2 tyrosine phosphatase plays multiple roles in IL-3 signal transduction, functioning in both catalytic-dependent and -independent manners in the Jak/Stat, Erk, and PI3 kinase pathways.

Indexed as

Milk ProteinsProto-Oncogene ProteinsAdaptor Proteins, Signal TransducingAnimalsCatalysisCell DivisionCell Line, TransformedCells, CulturedDNA-Binding ProteinsGene Transfer TechniquesHematopoietic Stem CellsHomeodomain ProteinsInterleukin-3Intracellular Signaling Peptides and ProteinsJanus Kinase 2MiceAdaptor Proteins, Signal TransducingDNA-Binding ProteinsGab1 protein, mouseHomeodomain ProteinsInterleukin-3Intracellular Signaling Peptides and ProteinsJak2 protein, mouseJanus Kinase 2Milk ProteinsMitogen-Activated Protein KinasesOncogene ProteinsPhosphatidylinositol 3-KinasesPhosphoproteinsProtein-Tyrosine KinasesProtein Tyrosine Phosphatase, Non-Receptor Type 11Protein Tyrosine PhosphatasesProto-Oncogene ProteinsPtpn11 protein, mouseReceptors, Interleukin-3STAT5 Transcription FactorTlx1 protein, mouseTrans-Activators

Identifiers

PMID12955078
OpenAlexW2024837443

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.