Evidence map›Paper›PMID 22863008›Full record

ArticleCell2012

HSF1 drives a transcriptional program distinct from heat shock to support highly malignant human cancers.

Marc L Mendillo, Sandro Santagata, Martina Koeva, George W Bell, Rong Hu, Rulla M Tamimi, Ernest Fraenkel, Tan A Ince, Luke Whitesell, Susan Lindquist

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 420 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
420citing papers in PubMed, 2 pooled it
22.1field-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

420 citing papers in PubMed, 2 syntheses or guidelines pooled it, 715 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  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. Proteostasis and ageing dissidence.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
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  8. Article
  9. Article
  10. Article
  11. Review
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  14. Article
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  16. Article
  17. Article
  18. Divergent condensates tune transcriptional responses during stress.bioRxiv : the preprint server for biology · 2026
    Article
  19. Article
  20. Article

360 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

10 authors at 6 institutions in 1 country.

Marc L MendilloThe Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Sandro Santagata
Martina Koeva
George W Bell
Rong Hu
Rulla M Tamimi
Ernest Fraenkel
Tan A Ince
Luke Whitesell
Susan Lindquist
Whitehead Institute for Biomedical Research · USMassachusetts Institute of Technology · USBrigham and Women's Hospital · USHarvard University · USHoward Hughes Medical Institute · USUniversity of Miami · US

Funding

Statistical MethodsP01CA087969 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI ROSNER, BERNARD A · 2000 to 2019
$77.8M
Variation in Receptor Tyrosine Kinases and Breast Cancer RiskP50CA089393 · NCI · DANA-FARBER CANCER INSTITUTE · PI HARRIS, LYNDSAY NORINE · 2000 to 2009
$28.8M
Epigenomic Mapping in Human Tumor Stem CellsR01CA146445 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI INCE, TAN A., LEE, TONG IHN · 2009 to 2013
$3.1M
A Systems Biology Approach to Reveal Huntington's Disease MechanismsR01GM089903 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FRAENKEL, ERNEST · 2010 to 2014
$2.4M
Heat Shock Directed Drug Discovery For The Treatment Of GliomasK08NS064168 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SANTAGATA, SANDRO · 2008 to 2012
$900k
Howard Hughes Medical InstituteNCI NIH HHS CA087969NCI NIH HHS CA089393NCI NIH HHS P01 CA087969NCI NIH HHS P50 CA089393NCI NIH HHS R01 CA146445NCI NIH HHS R01-CA146445-01NINDS NIH HHS K08 NS064168NINDS NIH HHS K08NS064168
6 · The paper itself

Abstract

Heat-Shock Factor 1 (HSF1), master regulator of the heat-shock response, facilitates malignant transformation, cancer cell survival, and proliferation in model systems. The common assumption is that these effects are mediated through regulation of heat-shock protein (HSP) expression. However, the transcriptional network that HSF1 coordinates directly in malignancy and its relationship to the heat-shock response have never been defined. By comparing cells with high and low malignant potential alongside their nontransformed counterparts, we identify an HSF1-regulated transcriptional program specific to highly malignant cells and distinct from heat shock. Cancer-specific genes in this program support oncogenic processes: cell-cycle regulation, signaling, metabolism, adhesion and translation. HSP genes are integral to this program, however, many are uniquely regulated in malignancy. This HSF1 cancer program is active in breast, colon and lung tumors isolated directly from human patients and is strongly associated with metastasis and death. Thus, HSF1 rewires the transcriptome in tumorigenesis, with prognostic and therapeutic implications.

Indexed as

Breast NeoplasmsCell Line, TumorCells, CulturedDNA-Binding ProteinsFemaleGene Expression Regulation, NeoplasticGene Regulatory NetworksGenome, HumanHeat Shock Transcription FactorsHumansNeoplasmsTranscription FactorsDNA-Binding ProteinsHeat Shock Transcription FactorsHSF1 protein, humanTranscription Factors

Identifiers

PMID22863008
PMCPMC3438889
OpenAlexW2153475997

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.