Evidence map›Paper›PMID 20452937›Full record

ReviewCold Spring Harbor perspectives in biology2010

Selectivity of the NF-{kappa}B response.

Ranjan Sen, Stephen T Smale

Open access · bronzeAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
–field-weighted citation impact
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

77 citing papers in PubMed, 143 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Aging and Inflammation.Cold Spring Harbor perspectives in medicine · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Redox Role of ROS and Inflammation in Pulmonary Diseases.Advances in experimental medicine and biology · 2021
    Review
  19. Article
  20. LOX-1 RegulatesFrontiers in cell and developmental biology · 2020
    Article

17 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

2 authors at 2 institutions in 1 country.

Ranjan SenLaboratory of Cellular and Molecular Biology, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21225, USA. ranjan.sen@nih.gov <ranjan.sen@nih.gov>
Stephen T Smale
National Institutes of Health · USUniversity of California, Los Angeles · US

Funding

NF-kB activation and function in B lymphocytesZIAAG000376 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, RANJAN · 2009 to 2025
$5.9M
Selective Regulation of Pro-Inflammatory Genes in MacrophagesR01GM086372 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALE, STEPHEN T · 2008 to 2015
$2.5M
Selective gene activation by the NF-kappaB family of transcription factorsR01AI073868 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALE, STEPHEN T · 2007 to 2011
$1.8M
Pro-inflammatory gene regulation in a native chromatin environmentR01CA127279 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALE, STEPHEN T · 2008 to 2011
$1.2M
High throughput screens for modulators of inflammatory cytakine gene expressionR21AI076921 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALE, STEPHEN T · 2009 to 2010
$403k
Intramural NIH HHSNCI NIH HHS R01 CA127279NIAID NIH HHS R01 AI073868NIAID NIH HHS R21 AI076921NIGMS NIH HHS R01 GM086372
6 · The paper itself

Abstract

NF-kappaB is activated by many stimuli and NF-kappaB binding sites have been identified in a wide variety of genes. Yet, NF-kappaB-dependent gene expression must be stimulus- and cell-type-specific. In others words, the cellular response to different NF-kappaB activating stimuli, such as TNFalpha, IL-1, and LPS, must be different; and the response of different cell types, such as lymphocytes, fibroblasts, or epithelial cells, to the same NF-kappaB-inducing stimulus must also be different. Finally, kinetics of gene expression must be accounted for, so that all NF-kappaB-dependent genes are not activated simultaneously even if cell type and stimulus are constant. Here, we explore the mechanistic framework in which such regulatory aspects of NF-kappaB-dependent gene expression have been analyzed because they are likely to form the basis for physiological responses.

Indexed as

AnimalsI-kappa B ProteinsInterleukin-1MiceNF-kappa BTumor Necrosis Factor-alphaI-kappa B ProteinsInterleukin-1NF-kappa BTumor Necrosis Factor-alpha

Identifiers

PMID20452937
PMCPMC2845200
OpenAlexW2154948069

What OpenQuestion holds

Textmetadata
LicenceTDM
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.