Evidence map›Paper›PMID 28852220›Full record

ReviewNature reviews. Molecular cell biology2018

Regulation of heat shock transcription factors and their roles in physiology and disease.

Rocio Gomez-Pastor, Eileen T Burchfiel, Dennis J Thiele

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 470 papers.

0numbers the graph read from it
0cells of the map it votes in
470citing papers in PubMed
24.1field-weighted citation impact, top 1% 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

470 citing papers in PubMed, 892 citations in OpenAlex.

  1. Article
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  4. More than the 'master regulator of cytosolic proteostasis': new roles for HSF1 in promoting tissue health.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  5. Adaptation to heat stress by diversification of the vertebrate heat shock transcription factor family.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  6. Article
  7. Principles and mechanisms of plant acclimation to heat stress.Nature reviews. Molecular cell biology · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Structural analysis ofbioRxiv : the preprint server for biology · 2026
    Article
  18. Article
  19. Article
  20. Update: Is exercise-induced oxidative stress a friend or foe?Sports medicine and health science · 2026
    Review

410 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

3 authors at 1 institution in 1 country.

Rocio Gomez-PastorDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine.
Eileen T BurchfielDepartment of Biochemistry, Duke University School of Medicine.
Dennis J ThieleDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine.
Duke University · US

Funding

Sensing and Responding to Cellular Protein MisfoldingF31GM119375 · NIGMS · DUKE UNIVERSITY · PI MOLZBERGER, EILEEN THERESE · 2016 to 2018
$114k
NIGMS NIH HHS F31 GM119375
6 · The paper itself

Abstract

The heat shock transcription factors (HSFs) were discovered over 30 years ago as direct transcriptional activators of genes regulated by thermal stress, encoding heat shock proteins. The accepted paradigm posited that HSFs exclusively activate the expression of protein chaperones in response to conditions that cause protein misfolding by recognizing a simple promoter binding site referred to as a heat shock element. However, we now realize that the mammalian family of HSFs comprises proteins that independently or in concert drive combinatorial gene regulation events that activate or repress transcription in different contexts. Advances in our understanding of HSF structure, post-translational modifications and the breadth of HSF-regulated target genes have revealed exciting new mechanisms that modulate HSFs and shed new light on their roles in physiology and pathology. For example, the ability of HSF1 to protect cells from proteotoxicity and cell death is impaired in neurodegenerative diseases but can be exploited by cancer cells to support their growth, survival and metastasis. These new insights into HSF structure, function and regulation should facilitate the development tof new disease therapeutics to manipulate this transcription factor family.

Indexed as

AnimalsGene Expression RegulationHeat-Shock ProteinsHeat-Shock ResponseHeat Shock Transcription FactorsHumansProtein Processing, Post-TranslationalTranscription, GeneticHeat-Shock ProteinsHeat Shock Transcription Factors

Identifiers

PMID28852220
PMCPMC5794010
OpenAlexW2750745925

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.