Evidence map›Paper›PMID 10077561›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Modulation of CREB binding protein function by the promyelocytic (PML) oncoprotein suggests a role for nuclear bodies in hormone signaling.

V Doucas, M Tini, D A Egan, R M Evans

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

67 citing papers in PubMed, 168 citations in OpenAlex.

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7 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

V DoucasSalk Institute for Biological Studies, La Jolla, CA 92037, USA. doucas@cmu.unige.ch
M Tini
D A Egan
R M Evans
Howard Hughes Medical Institute · USSalk Institute for Biological Studies · USUniversity of Geneva · CH

Funding

TRANSCRIPTIONAL REGULATION OF T-CELL RECEPTOR ALPHA GENEP01CA054418 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI VERMA, INDER MOHAN · 1991 to 2005
$14.1M
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR01GM026444 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M. · 1985 to 1989
–
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR37GM026444 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M. · 1990 to 1999
–
NCI NIH HHS P01 CA054418NIGMS NIH HHS GM26444
6 · The paper itself

Abstract

Disaggregation of the spherical nuclear bodies termed promyelocytic (PML) oncogenic domains (PODs) is a characteristic of acute promyelocytic leukemia. Here, we demonstrate that the cAMP enhancer binding protein (CREB)-binding protein (CBP) associates with PML in vitro and is recruited to the PODs in vivo. Through its association with CBP, wild-type PML dramatically stimulates nuclear receptor transcriptional activity. These results demonstrate that a fraction of CBP is compartmentalized to the POD through its association with PML and thus suggest that PML and other POD-associated proteins may play an unexpectedly broad role in aspects of transcriptional regulation and human disease.

Indexed as

Cell CompartmentationCell NucleusCREB-Binding ProteinGene Expression Regulation, NeoplasticHumansLeukemia, Promyelocytic, AcuteNeoplasm ProteinsNuclear ProteinsPromyelocytic Leukemia ProteinTrans-ActivatorsTranscriptional ActivationTranscription FactorsTumor Suppressor ProteinsCREB-Binding ProteinCREBBP protein, humanNeoplasm ProteinsNuclear ProteinsPML protein, humanPromyelocytic Leukemia ProteinTrans-ActivatorsTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID10077561
PMCPMC15819
OpenAlexW1990565764

What OpenQuestion holds

Texttitle and abstract
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.