Evidence map›Paper›PMID 17599039›Full record

ArticleOncogene2008

Egr-1 abrogates the E2F-1 block in terminal myeloid differentiation and suppresses leukemia.

J D Gibbs, D A Liebermann, B Hoffman

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Tumor regression efficacy ofBioinformation · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. CaAdvances in cancer research · 2020
    Review
  10. Article
  11. Blood · 2018
    Article
  12. Review
  13. Article
  14. The progress of early growth response factor 1 and leukemia.Intractable & rare diseases research · 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

3 authors at 1 institution in 1 country.

J D GibbsFels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, PA, USA.
D A Liebermann
B Hoffman
Temple University · US

Funding

NEGATIVE REGULATORS OF MYELOPOIESISR01CA081168 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI HOFFMAN, BARBARA · 1999 to 2009
$2.4M
NCI NIH HHS R01 CA081168
6 · The paper itself

Abstract

Deregulated growth and blocks in differentiation collaborate in the multistage process of leukemogenesis. Previously, we have shown that ectopic expression of the zinc finger transcription factor Egr-1 in M1 myeloblastic leukemia cells promotes terminal differentiation with interleukin-6 (IL-6). In addition, we have shown that deregulated expression of the oncogene E2F-1 blocks the myeloid terminal differentiation program, resulting in proliferation of immature cells in the presence of IL-6. Here it is shown that the positive regulator of differentiation Egr-1 abrogates the E2F-1-driven block in myeloid terminal differentiation. The M1E2F-1/Egr-1 cells underwent G(0)/G(1) arrest and functional macrophage maturation following treatment with IL-6. Furthermore, Egr-1 diminished the aggressiveness of M1E2F-1 leukemias and abrogated the leukemic potential of IL-6-treated M1E2F-1 cells. Previously, we reported that Egr-1 abrogated the block in terminal myeloid differentiation imparted by deregulated c-myc, which blocks differentiation at a later stage than E2F-1, resulting in cells that have the characteristics of functionally mature macrophages that did not undergo G(0)/G(1) arrest. Taken together, this work extends and highlights the tumor suppressor role of Egr-1, with Egr-1 behaving as a tumor suppressor against two oncogenes, each blocking myeloid differentiation by a different mechanism. These findings suggest that Egr-1 and/or Egr-1 target genes may be useful tools to treat or suppress oncogene-driven hematological malignancies.

Indexed as

AnimalsApoptosisCell DifferentiationCell Line, TumorE2F1 Transcription FactorEarly Growth Response Protein 1Growth InhibitorsInterleukin-6Leukemia, Myeloid, AcuteMacrophagesMiceMice, NudeMyeloid CellsTumor Suppressor ProteinsE2F1 protein, humanE2f1 protein, mouseE2F1 Transcription FactorEarly Growth Response Protein 1Egr1 protein, mouseGrowth InhibitorsInterleukin-6Tumor Suppressor Proteins

Identifiers

PMID17599039
OpenAlexW2091861204

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.