Evidence map›Paper›PMID 23792173›Full record

ReviewMolecular and cellular endocrinology2013

Variable steroid receptor responses: Intrinsically disordered AF1 is the key.

S Stoney Simons, Raj Kumar

Abstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 43 citations in OpenAlex.

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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 2 institutions in 1 country.

S Stoney SimonsSteroid Hormones Section, NIDDK/LERB, National Institutes of Health, Bethesda, MD, United States. stoneys@helix.nih.gov
Raj Kumar
Commonwealth Medical College · USNational Institute of Diabetes and Digestive and Kidney Diseases · US

Funding

Modulation of parameters of glucocorticoid receptor-mediated gene inductionZIADK057800 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SIMONS, S STONEY · 2009 to 2015
$2.6M
Modulation of parameters of glucocorticoid receptor-mediated gene repressionZIADK047040 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SIMONS, S STONEY · 2009 to 2015
$2.0M
Mechanisms for glucocorticoid vs. progesterone receptor-specific gene regulationZIADK047041 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SIMONS, S STONEY · 2009 to 2014
$1.3M
Modulation of parameters of glucocorticoid receptor-mediated gene inductionZ01DK057800 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SIMONS, S STONEY · 1992 to 2008
$587k
Modulation of glucocorticoid receptor-mediated gene induction by chemicalsZIADK075066 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SIMONS, S STONEY · 2012 to 2014
$432k
Intramural NIH HHS Z01 DK057800Intramural NIH HHS ZIA DK047041Intramural NIH HHS ZIA DK057800
6 · The paper itself

Abstract

Steroid hormones, acting through their cognate receptor proteins, see widespread clinical applications due to their ability to alter the induction or repression of numerous genes. However, steroid usage is limited by the current inability to control off-target, or non-specific, side-effects. Recent results from three separate areas of research with glucocorticoid and other steroid receptors (cofactor-induced changes in receptor structure, the ability of ligands to alter remote regions of receptor structure, and how cofactor concentration affects both ligand potency and efficacy) indicate that a key element of receptor activity is the intrinsically disordered amino-terminal domain. These results are combined to construct a novel framework within which to logically pursue various approaches that could afford increased selectivity in steroid-based therapies.

Indexed as

HormonesHumansLigandsProtein BindingProtein FoldingProtein Structure, TertiaryReceptors, SteroidSignal TransductionSteroidsTranscriptional ActivationHormonesLigandsReceptors, SteroidSteroidsAF1 domain as a molecular rheostatA(max) and EC(50)Intrinsically disordered domainsSelective receptor modulators (SRMs)Selectivity in controlling gene expressionSteroid receptors

Identifiers

PMID23792173
PMCPMC3781172
OpenAlexW1973174127

What OpenQuestion holds

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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.