Evidence map›Paper›PMID 15800671›Full record

ArticleLeukemia2005

ZAP-70 is expressed by a subset of normal human B-lymphocytes displaying an activated phenotype.

J C Nolz, R C Tschumper, B T Pittner, J R Darce, N E Kay, D F Jelinek

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Beyond TCR Signaling: Emerging Functions of Lck in Cancer and Immunotherapy.International journal of molecular sciences · 2019
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Detection methods of ZAP-70 in chronic lymphocytic leukemia.Clinical and experimental medicine · 2012
    Review
  12. Article
  13. Review
  14. Review
  15. Chronic lymphocytic leukaemia: a disease of activated monoclonal B cells.Best practice & research. Clinical haematology · 2010
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Prognostic factors in chronic lymphocytic leukemia.Current hematologic malignancy reports · 2007
    Review
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

6 authors at 2 institutions in 1 country.

J C NolzDepartment of Immunology, Mayo Clinic College of Medicine, Mayo Graduate School, Rochester, MN 55905, USA.
R C Tschumper
B T Pittner
J R Darce
N E Kay
D F Jelinek
Mayo Clinic · USMayo Clinic in Arizona · US

Funding

MULTIDISCIPLINARY TRAINING IN EXPERIMENTAL HEMATOLOGYT32HL067742 · NHLBI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI KAUFMANN, SCOTT H · 2001 to 2005
$661k
NHLBI NIH HHS 5-T32-HL67742
6 · The paper itself

Abstract

The Syk family tyrosine kinase ZAP-70 is essential for normal T-cell development and signaling. Recently, leukemic cells from some patients with B-cell chronic lymphocytic leukemia (B-CLL) were shown to express ZAP-70. Owing to the prognostic value of B-CLL ZAP-70 expression, this phenotype may reflect intrinsic biological differences between the two subsets of disease. However, it remains unclear whether CLL-B cells aberrantly acquire ZAP-70 expression during the transformation process or whether ZAP-70 may be expressed under certain conditions in normal human B-lymphocytes. To discriminate between these two possibilities, we assessed ZAP-70 expression in normal human B-lymphocytes. Our data demonstrate that ZAP-70 is expressed in a subpopulation of tonsillar and splenic normal B-lymphocytes that express an activated phenotype. Furthermore, ZAP-70 expression can be induced in vitro upon stimulation of blood and tonsillar B cells. Finally, we show that phosphorylation of ZAP-70 occurs in tonsillar B cells with stimulation through the B-cell receptor. These results provide new insight into normal human B-cell biology as well as provide clues about the transformed cell in B-CLL.

Indexed as

B-LymphocytesCell DifferentiationFlow CytometryHumansJurkat CellsLymphocyte ActivationLymphocyte SubsetsPalatine TonsilPhenotypePhosphorylationProtein-Tyrosine KinasesSpleenTransfectionZAP-70 Protein-Tyrosine KinaseProtein-Tyrosine KinasesZAP70 protein, humanZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID15800671
OpenAlexW1985310121

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.