Evidence map›Paper›PMID 24556212›Full record

ArticleHuman molecular genetics2014

Contesting the dogma of an age-related heat shock response impairment: implications for cardiac-specific age-related disorders.

Alisia Carnemolla, John P Labbadia, Hayley Lazell, Andreas Neueder, Saliha Moussaoui, Gillian P Bates

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Biomolecular Markers of Brain Aging.Advances in experimental medicine and biology · 2023
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Cellular proteostasis decline in human senescence.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Review
  14. Article
  15. Heat-Shock Proteins in Neuroinflammation.Frontiers in pharmacology · 2019
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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

6 authors at 2 institutions in 2 countries.

Alisia CarnemollaDepartment Medical and Molecular Genetics, King's College London, 8th Floor Tower Wing, Guy's Hosptial, Great Maze Pond, London SE1 9RT, UK.
John P LabbadiaDepartment Medical and Molecular Genetics, King's College London, 8th Floor Tower Wing, Guy's Hosptial, Great Maze Pond, London SE1 9RT, UK.
Hayley LazellDepartment Medical and Molecular Genetics, King's College London, 8th Floor Tower Wing, Guy's Hosptial, Great Maze Pond, London SE1 9RT, UK.
Andreas NeuederDepartment Medical and Molecular Genetics, King's College London, 8th Floor Tower Wing, Guy's Hosptial, Great Maze Pond, London SE1 9RT, UK.
Saliha MoussaouiNovartis Institute for Biomedical Research, Neuroscience Discovery, Basel CH-4002, Switzerland.
Gillian P BatesDepartment Medical and Molecular Genetics, King's College London, 8th Floor Tower Wing, Guy's Hosptial, Great Maze Pond, London SE1 9RT, UK gillian.bates@kcl.ac.uk.
King's College London · GBNovartis (Switzerland) · CH

Funding

Medical Research Council G0801314
6 · The paper itself

Abstract

Ageing is associated with the reduced performance of physiological processes and has been proposed as a major risk factor for disease. An age-related decline in stress response pathways has been widely documented in lower organisms. In particular, the heat shock response (HSR) becomes severely compromised with age in Caenorhabditis elegans. However, a comprehensive analysis of the consequences of ageing on the HSR in higher organisms has not been documented. We used both HS and inhibition of HSP90 to induce the HSR in wild-type mice at 3 and 22 months of age to investigate the extent to which different brain regions, and peripheral tissues can sustain HSF1 activity and HS protein (HSP) expression with age. Using chromatin immunoprecipitation, quantitative reverse transcription polymerase chain reaction, western blotting and enzyme linked immunosorbent assay (ELISA), we were unable to detect a difference in the level or kinetics of HSP expression between young and old mice in all brain regions. In contrast, we did observe an age-related reduction in chaperone levels and HSR-related proteins in the heart. This could result in a decrease in the protein folding capacity of old hearts with implications for age-related cardiac disorders.

Indexed as

Heat-Shock ResponseAgingAnimalsBrainDNA-Binding ProteinsFemaleGene Expression Regulation, DevelopmentalHeartHeat-Shock ProteinsHeat Shock Transcription FactorsMaleMiceMice, Inbred C57BLMice, Inbred CBAMyocardiumProtein Folding2-amino-7-(4-fluoro-2-(6-methoxypyridin-2-yl)phenyl)-4-methyl-7,8-dihydropyrido(4,3-d)pyrimidin-5(6H)-oneDNA-Binding ProteinsHeat-Shock ProteinsHeat Shock Transcription FactorsHsf1 protein, mousePyridonesPyrimidinesTranscription Factors

Identifiers

PMID24556212
PMCPMC4065144
OpenAlexW2131263697

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.