Evidence map›Paper›PMID 7565701›Full record

ArticleMolecular and cellular biology1995

The zinc finger transcription factor Egr-1 potentiates macrophage differentiation of hematopoietic cells.

K Krishnaraju, H Q Nguyen, D A Liebermann, B Hoffman

Abstract read
In one paragraph

Article in Molecular and cellular biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

45 citing papers in PubMed, 132 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Inflammation in Focus: The Beginning and the End.Pathology oncology research : POR · 2021
    Review
  6. Cellular and molecular events of inflammation induced transdifferentiation (EMT) and regeneration (MET) in mesenteric mesothelial cells.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. The Molecular Mechanisms of Plant-Derived Compounds Targeting Brain Cancer.International journal of molecular sciences · 2018
    Review
  11. Metallothioneins: Emerging Modulators in Immunity and Infection.International journal of molecular sciences · 2017
    Review
  12. Article
  13. Review
  14. Molecular targets of curcumin for cancer therapy: an updated review.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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 1 institution in 1 country.

K KrishnarajuFels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
H Q Nguyen
D A Liebermann
B Hoffman
Temple University · US

Funding

MYELOPOIESIS, LEUKEMIA &ITS SUPPRESSION: MOLECULAR GENER01CA043618 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LIEBERMANN, DAN A · 1990 to 2000
$270k
GENE DISSECTION OF MYELOID DIFFERENTIATION &LEUKEMIASR01CA051162 · NCI · UNIVERSITY OF PENNSYLVANIA · PI HOFFMAN, BARBARA · 1992 to 1996
–
NUCLEAR REGULATORS IN MYELOPOIESIS AND LEUKEMIAR01CA059774 · NCI · TEMPLE UNIVERSITY · PI LIEBERMANN, DAN A · 1994 to 1998
–
NCI NIH HHS 1RO1CA43618NCI NIH HHS 1RO1CA51162NCI NIH HHS 1RO1CA59774
6 · The paper itself

Abstract

Previously we have shown that the zinc finger transcription factor Egr-1 is essential for and restricts differentiation of hematopoietic cells along the macrophage lineage, raising the possibility that Egr-1 actually plays a deterministic role in governing the development of hematopoietic precursor cells along the monocytic lineage. To test this hypothesis, we have taken advantage of interleukin-3-dependent 32Dcl3 hematopoietic precursor cells which, in addition to undergoing granulocytic differentiation in response to granulocyte colony-stimulating factor, were found to be induced for limited proliferation, but not differentiation, by granulocyte-macrophage colony-stimulating factor. It was shown that ectopic expression of Egr-1 blocked granulocyte colony-stimulating factor-induced terminal granulocytic differentiation, consistent with previous findings. In addition, ectopic expression of Egr-1 endowed 32Dcl3 cells with ability to be induced by granulocyte-macrophage colony-stimulating factor for terminal differentiation exclusively along the macrophage lineage. Thus, evidence that Egr-1 potentiates terminal macrophage differentiation has been obtained, suggesting that Egr-1 plays a deterministic role in governing the development of hematopoietic cells along the macrophage lineage.

Indexed as

Immediate-Early ProteinsZinc FingersAnimalsCell DifferentiationCell DivisionCell LineDNA-Binding ProteinsEarly Growth Response Protein 1Gene ExpressionGranulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorGranulocytesHematopoiesisHematopoietic Stem CellsInterleukin-3MacrophagesDNA-Binding ProteinsEarly Growth Response Protein 1Egr1 protein, mouseGranulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorImmediate-Early ProteinsInterleukin-3RNA, MessengerTranscription Factors

Identifiers

PMID7565701
PMCPMC230800
OpenAlexW2148381523

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.