Evidence map›Paper›PMID 18174918›Full record

ReviewNuclear receptor signaling2007

MTA family of coregulators in nuclear receptor biology and pathology.

Bramanandam Manavathi, Kamini Singh, Rakesh Kumar

Open access · hybridAbstract readReview
In one paragraph

Review in Nuclear receptor signaling, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
2.8field-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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. MTA1 Expression in Benign and Malignant Salivary gland Tumors.Iranian journal of otorhinolaryngology · 2016
    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.

Bramanandam ManavathiDepartment of Molecular and Cellular Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA.
Kamini Singh
Rakesh Kumar
The University of Texas MD Anderson Cancer Center · US

Funding

Role of Metastatic Tumor Antigen-1 in Mammary GlandR01CA098823 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 2003 to 2013
$3.1M
RECEPTOR BLOCKADE FOR BREAST CANCERR01CA065746 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 1999 to 2007
$1.9M
SERM Regulation of PAK Pathway in Endometrial CancerR01CA109379 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 2004 to 2008
$1.5M
LABORATORY STUDY OF CHEMOTHERAPY PLUS RECEPTOR BLOCKADEU01CA065746 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI MENDELSOHN, JOHN · 1995 to 1998
–
NCI NIH HHS CA109379NCI NIH HHS CA65746NCI NIH HHS CA98823NCI NIH HHS R01 CA065746NCI NIH HHS R01 CA098823NCI NIH HHS R01 CA109379NCI NIH HHS U01 CA065746
6 · The paper itself

Abstract

Nuclear receptors (NRs) rely on coregulators (coactivators and corepressors) to modulate the transcription of target genes. By interacting with nucleosome remodeling complexes, NR coactivators potentiate transcription, whereas corepressors inhibit transcription of the target genes. Metastasis-associated proteins (MTA) represent an emerging family of novel NR coregulators. In general, MTA family members form independent nucleosome remodeling and deacetylation (NuRD) complexes and repress the transcription of different genes by recruiting histone deacetylases onto their target genes. However, MTA1 also acts as a coactivator in a promoter-context dependent manner. Recent findings that repression of estrogen receptor transactivation functions by MTA1, MTA1s, and MTA2 and regulation of MTA3 by estrogen signaling have indicated the significance of these proteins in NR signaling. Here, we highlight the action of MTA proteins on NR signaling and their roles in pathophysiological conditions.

Indexed as

Signal TransductionAnimalsApoptosis Regulatory ProteinsCell NucleusHumansNeoplasm MetastasisNeoplasm ProteinsNuclear ProteinsRepressor ProteinsApoptosis Regulatory ProteinsNeoplasm ProteinsNuclear ProteinsRepressor Proteins

Identifiers

PMID18174918
PMCPMC2121320
OpenAlexW2069928663

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.