Evidence map›Paper›PMID 8628295›Full record

ArticleMolecular and cellular biology1996

Role of EGR1 in regulation of stimulus-dependent CD44 transcription in B lymphocytes.

J S Maltzman, J A Carman, J G Monroe

Abstract read
In one paragraph

Article in Molecular and cellular biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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

31 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Targeting Cancer Stem Cells in Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Hyaluronan promotes the chondrocyte response to BMP-7.Osteoarthritis and cartilage · 2009
    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

3 authors.

J S MaltzmanDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, School of Medicine, Philadelphia, 19104, USA.
J A Carman
J G Monroe

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007170 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BRASS, LAWRENCE F · 1985 to 2022
$54.0M
REGULATED B-CELL UNRESPONSIVENESS AND TOLERANCER01AI032592 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI CHOI, YONGWON · 1993 to 2011
$3.9M
STUDIES OF RECEPTOR IMMUNOGLOBULIN MEDIATED SIGNALLINGR01AI023568 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI MONROE, JOHN G · 1990 to 2000
$271k
STUDIES OF RECEPTOR IMMUNOGLOBULIN MEDIATED SIGNALLINGR23AI023568 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI MONROE, JOHN G · 1985 to 1987
–
NIAID NIH HHS AI-23568NIAID NIH HHS AI-32592NIGMS NIH HHS 5-T32-GM-07170
6 · The paper itself

Abstract

The immediate-early gene egr-1 encodes a transcription factor (EGR1) that links B-cell antigen receptor (BCR) signals to downstream activation events through the regulation of previously unidentified target genes. Here we identify the gene encoding the lymphocyte homing and migration protein CD44 as a target of EGR1 regulation in B cells. BCR-induced increases in CD44 mRNA expression and transcription levels are shown to occur in EGR1-expressing but not in nonexpressing subclones of the B-cell line WEHI-231. Kinetics of egr-1 transcription and the appearance of nuclear EGR1 protein precede CD44 induction and occur within 30 min after stimulation in the EGR1-expressing subclone. A single EGR1 binding motif is demonstrated at bp -301 of the human CD44 promoter. Cotransfection of a CD44 promoter-chloramphenicol acetyltransferase reporter construct with an egr-1 expression vector resulted in a 6.5- to 8.5-fold induction of transcriptional activity relative to an empty expression vector. The EGR1 binding motif was shown to be necessary for stimulus-induced expression of a CD44 promoter-chloramphenicol acetyltransferase reporter construct in nontransformed B lymphocytes and was required for transactivation by an EGR1 expression vector in a B-cell line. These studies identify EGR1 as an intermediary linking BCR-derived signals to the induction of CD44. The relevance of these molecular events to BCR signal transduction and antigen-stimulated B-cell-mediated immune responses is discussed.

Indexed as

Gene Expression RegulationImmediate-Early ProteinsTranscription, GeneticAnimalsAntibody FormationBase SequenceBinding SitesB-LymphocytesCell NucleusCells, CulturedChloramphenicol O-AcetyltransferaseDNA-Binding ProteinsDNA PrimersEarly Growth Response Protein 1Early Growth Response Protein 2Escherichia coliChloramphenicol O-AcetyltransferaseDNA-Binding ProteinsDNA PrimersEarly Growth Response Protein 1Early Growth Response Protein 2EGR1 protein, humanEgr1 protein, mouseEGR2 protein, humanEgr2 protein, mouseHyaluronan ReceptorsImmediate-Early ProteinsLipopolysaccharidesOligonucleotide ProbesProto-Oncogene Proteins c-junProto-Oncogene Proteins c-mycRecombinant Fusion ProteinsRNA, MessengerTetradecanoylphorbol AcetateTranscription Factors

Identifiers

PMID8628295
PMCPMC231216

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.