Evidence map›Paper›PMID 17349961›Full record

ArticleMolecular cell2007

An essential function of the SRC-3 coactivator in suppression of cytokine mRNA translation and inflammatory response.

Chundong Yu, Brian York, Shu Wang, Qin Feng, Jianming Xu, Bert W O'Malley

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
6.8field-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

85 citing papers in PubMed, 131 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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  7. Article
  8. T-Cell Intracellular Antigen 1-Like Protein in Physiology and Pathology.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. SRC-3, a Steroid Receptor Coactivator: Implication in Cancer.International journal of molecular sciences · 2021
    Review
  17. Review
  18. Article
  19. Review
  20. Molecular mechanisms of stress granule assembly and disassembly.Biochimica et biophysica acta. Molecular cell research · 2021
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Chundong YuDepartment of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
Brian York
Shu Wang
Qin Feng
Jianming Xu
Bert W O'Malley
Baylor College of Medicine · US

Funding

ProteomicsU19DK062434 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MANGELSDORF, DAVID J · 2002 to 2011
$37.4M
TISSUE COACTIVATOR AND RECEPTOR EXPRESSION FINGERPRINTSP01DK059820 · NIDDK · INSTITUT DE GENETIQUE ET BIOLOGIE MOLECU · PI O'MALLEY, BERT W · 2001 to 2016
$23.1M
REPRODUCTIVE HORMONES: BIOLOGICAL AND MOLECULAR ACTIONSR01HD008188 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI DAVID M LONARD, JOHN P LYDON · 1985 to 2026
$16.3M
Role of SRC-3 in LPS-induced inflammation responseF32GM072235 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI YU, CHUNDONG · 2004 to 2005
$91k
NICHD NIH HHS R01 HD008188NIDDK NIH HHS P01 DK059820NIDDK NIH HHS U19 DK062434NIGMS NIH HHS F32 GM 072235NIGMS NIH HHS F32 GM072235
6 · The paper itself

Abstract

Steroid receptor coactivator-3 (SRC-3) is a transcriptional coactivator for nuclear receptors and other transcription factors. Although multiple physiological roles of SRC-3 have been revealed, its involvement in the inflammatory process remains unclear. Herein we show that SRC-3(-/-) mice are markedly hypersensitive to LPS-induced endotoxic shock. In response to LPS, SRC-3(-/-) macrophages produce significantly more proinflammatory cytokines such as TNF-alpha, IL-6, and IL-1beta than wild-type controls, although they express similar amounts of cytokine mRNAs, suggesting that SRC-3 can exert effects at translational levels. Increased heavy polysome-associated TNF-alpha and IL-1beta mRNAs in SRC-3(-/-) macrophages implicate SRC-3 as a translational repressor. SRC-3 may cooperate with other translational repressors such as TIA-1 and TIAR to regulate cytokine mRNA translation. Collectively, our studies reveal an essential function of SRC-3 as a coordinator of inflammatory mRNA translation and as a physiologic protective factor against the lethal endotoxic shock triggered by an acute inflammatory response.

Indexed as

InflammationAnimalsCytokinesFemaleHeLa CellsHistone AcetyltransferasesHumansLipopolysaccharidesMacrophages, PeritonealMaleMiceNuclear Receptor Coactivator 3Protein BindingProtein BiosynthesisReceptors, GlucocorticoidRepressor ProteinsCytokinesHistone AcetyltransferasesLipopolysaccharidesNCOA3 protein, humanNcoa3 protein, mouseNuclear Receptor Coactivator 3Receptors, GlucocorticoidRepressor ProteinsRNA-Binding ProteinsT-Cell Intracellular Antigen-1Tia1 protein, mouseTial1 protein, mouseTrans-ActivatorsTumor Necrosis Factor-alpha

Identifiers

PMID17349961
PMCPMC1864954
OpenAlexW2060700554

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.