Evidence map›Paper›PMID 15601827›Full record

ArticleMolecular and cellular biology2005

Neutrophil elastase is important for PML-retinoic acid receptor alpha activities in early myeloid cells.

Andrew A Lane, Timothy J Ley

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. 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
1.6field-weighted citation impact, top 18% 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, 49 citations in OpenAlex.

  1. Article
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  8. The PML domain of PML-RARα blocks senescence to promote leukemia.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
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  10. Review
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  12. Effect of GINS2 on proliferation and apoptosis in leukemic cell line.International journal of medical sciences · 2013
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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

2 authors at 1 institution in 1 country.

Andrew A LaneDepartments of Medicine and Genetics, Division of Oncology, Siteman Cancer Center, Washington University, 660 S. Euclid Ave., Campus Box 8007, St. Louis, MO 63110-1093, USA. tley@im.wustl.edu
Timothy J Ley
Washington University in St. Louis · US

Funding

PRE-AND POSTGRADUATE TRAINING IN MOLECULAR HEMATOLOGYT32HL007088 · NHLBI · WASHINGTON UNIVERSITY · PI Grant Anthony Challen, Stephen Oh · 1985 to 2026
$14.1M
THE BIOLOGY OF PROMYELOCYTIC LEUKEMIA IN A MOUSE MODEL.R01CA083962 · NCI · WASHINGTON UNIVERSITY · PI LEY, TIMOTHY J. · 2000 to 2014
$6.0M
NCI NIH HHS CA 83962NCI NIH HHS R01 CA083962NHLBI NIH HHS T32 HL007088NHLBI NIH HHS T32 HL 07088
6 · The paper itself

Abstract

Expression of the PML-retinoic acid receptor alpha (PML-RARalpha) fusion protein is the initiating genetic event for acute promyelocytic leukemia (APL), but the molecular mechanisms responsible for disease initiation are not yet clear. Several observations have suggested that early myeloid cells are uniquely susceptible to transformation by PML-RARalpha. Recently, we have shown that the early myeloid-specific protease neutrophil elastase is important for APL development in the mouse. To better understand the role of neutrophil elastase for the pathogenesis of APL, we examined the consequences of PML-RARalpha expression in early myeloid cells with or without neutrophil elastase. We found that high-level PML-RARalpha expression was associated with cellular toxicity that was dependent on the expression of neutrophil elastase; a mutant form of PML-RARalpha that resisted neutrophil elastase cleavage was not toxic. When PML-RARalpha was expressed at very low levels in the early myeloid cells of mice, it induced myeloid expansion and delayed myeloid maturation; neutrophil elastase was also required for these activities. The activities of PML-RARalpha in early myeloid cells are therefore strongly influenced by the presence of neutrophil elastase. To assure physiologic relevance, PML-RARalpha functions should be evaluated in neutrophil elastase-expressing early myeloid cells.

Indexed as

AnimalsBlotting, WesternCell DifferentiationCell Line, TumorCell ProliferationFemaleGreen Fluorescent ProteinsHL-60 CellsHumansIn Situ Nick-End LabelingK562 CellsLeukemia, Promyelocytic, AcuteLeukocyte ElastaseMaleMiceMice, Inbred C3HGreen Fluorescent ProteinsLeukocyte ElastaseNeoplasm ProteinsOncogene Proteins, Fusionpromyelocytic leukemia-retinoic acid receptor alpha fusion oncoproteinRARA protein, humanRara protein, mouseReceptors, Retinoic AcidRetinoic Acid Receptor alpha

Identifiers

PMID15601827
PMCPMC538790
OpenAlexW2153680238

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.