Evidence map›Paper›PMID 15744343›Full record

ArticleLeukemia2005

ID1 and ID2 are retinoic acid responsive genes and induce a G0/G1 accumulation in acute promyelocytic leukemia cells.

J Nigten, M C Breems-de Ridder, C A J Erpelinck-Verschueren, G Nikoloski, B A van der Reijden, S van Wageningen, P B van Hennik, T de Witte, B Löwenberg, J H Jansen

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Article in Leukemia, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. High bone marrowOncotarget · 2017
    Article
  7. Article
  8. Clinical significance of up-regulated ID1 expression in Chinese de novo acute myeloid leukemia.International journal of clinical and experimental pathology · 2015
    Article
  9. Article
  10. Article
  11. Article
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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

10 authors at 3 institutions in 1 country.

J NigtenCentral Hematology Laboratory and Department of Hematology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
M C Breems-de Ridder
C A J Erpelinck-Verschueren
G Nikoloski
B A van der Reijden
S van Wageningen
P B van Hennik
T de Witte
B Löwenberg
J H Jansen
Erasmus MC · NLRadboud University Medical Center · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute promyelocytic leukemia (APL) is uniquely sensitive to treatment with all-trans retinoic acid (ATRA), which results in the expression of genes that induce the terminal granulocytic differentiation of the leukemic blasts. Here we report the identification of two ATRA responsive genes in APL cells, ID1 and ID2. These proteins act as antagonists of basic helix-loop-helix (bHLH) transcription factors. ATRA induced a rapid increase in ID1 and ID2, both in the APL cell line NB4 as well as in primary patient cells. In addition, a strong downregulation of E2A was observed. E2A acts as a general heterodimerization partner for many bHLH proteins that are involved in differentiation control in various tissues. The simultaneous upregulation of ID1 and ID2, and the downregulation of E2A suggest a role for bHLH proteins in the induction of differentiation of APL cells following ATRA treatment. To test the relevance of this upregulation, ID1 and ID2 were overexpressed in NB4 cells. Overexpression inhibited proliferation and induced a G0/G1 accumulation. These results indicate that ID1 and ID2 are important retinoic acid responsive genes in APL, and suggest that the inhibition of specific bHLH transcription factor complexes may play a role in the therapeutic effect of ATRA in APL.

Indexed as

DNA-Binding ProteinsRepressor ProteinsTranscription FactorsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell Line, TumorCell ProliferationCells, CulturedClone CellsColony-Forming Units AssayDose-Response Relationship, DrugG1 PhaseGene Expression Regulation, NeoplasticHumansInhibitor of Differentiation Protein 1Inhibitor of Differentiation Protein 2Basic Helix-Loop-Helix ProteinsDNA-Binding ProteinsID1 protein, humanID2 protein, humanInhibitor of Differentiation Protein 1Inhibitor of Differentiation Protein 2Repressor ProteinsTCF3 protein, humanTranscription FactorsTretinoin

Identifiers

PMID15744343
OpenAlexW2122478354

What OpenQuestion holds

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Registered trials

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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.