Evidence map›Paper›PMID 30338738›Full record

ReviewCurrent cancer drug targets2019

HSF1 as a Cancer Biomarker and Therapeutic Target.

Richard L Carpenter, Yesim Gökmen-Polar

Open access · greenAbstract readReview
In one paragraph

Review in Current cancer drug targets, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

69 citing papers in PubMed, 126 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
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  9. Review
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  11. Article
  12. HSF1 Activation Mechanisms, Disease Roles, and Small Molecule Therapeutics.International journal of biological sciences · 2025
    Review
  13. Article
  14. HSF1 is a prognostic determinant and therapeutic target in intrahepatic cholangiocarcinoma.Journal of experimental & clinical cancer research : CR · 2024
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

9 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 1 institution in 1 country.

Richard L CarpenterMelvin and Bren Simon Cancer Center, Indiana University School of Medicine, Bloomington, IN 47405, United States.
Yesim Gökmen-PolarMelvin and Bren Simon Cancer Center, Indiana University School of Medicine, Bloomington, IN 47405, United States.
Indiana University School of Medicine

Funding

Functional interactions between AKT and HSF-1 in breast cancer progressionK22CA207575 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI CARPENTER, RICHARD L · 2017 to 2019
$486k
NCI NIH HHS K22 CA207575
6 · The paper itself

Abstract

Heat shock factor 1 (HSF1) was discovered in 1984 as the master regulator of the heat shock response. In this classical role, HSF1 is activated following cellular stresses such as heat shock that ultimately lead to HSF1-mediated expression of heat shock proteins to protect the proteome and survive these acute stresses. However, it is now becoming clear that HSF1 also plays a significant role in several diseases, perhaps none more prominent than cancer. HSF1 appears to have a pleiotropic role in cancer by supporting multiple facets of malignancy including migration, invasion, proliferation, and cancer cell metabolism among others. Because of these functions, and others, of HSF1, it has been investigated as a biomarker for patient outcomes in multiple cancer types. HSF1 expression alone was predictive for patient outcomes in multiple cancer types but in other instances, markers for HSF1 activity were more predictive. Clearly, further work is needed to tease out which markers are most representative of the tumor promoting effects of HSF1. Additionally, there have been several attempts at developing small molecule inhibitors to reduce HSF1 activity. All of these HSF1 inhibitors are still in preclinical models but have shown varying levels of efficacy at suppressing tumor growth. The growth of research related to HSF1 in cancer has been enormous over the last decade with many new functions of HSF1 discovered along the way. In order for these discoveries to reach clinical impact, further development of HSF1 as a biomarker or therapeutic target needs to be continued.

Indexed as

Antineoplastic AgentsBiomarkers, TumorHeat Shock Transcription FactorsHumansMolecular Targeted TherapyNeoplasmsAntineoplastic AgentsBiomarkers, TumorHeat Shock Transcription FactorsHSF1 protein, humanbiomarkerEMTHSF1invasionmetastasismigrationtherapy.

Identifiers

PMID30338738
PMCPMC6472998
OpenAlexW2896328850

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.