Evidence map›Paper›PMID 39889818›Full record

ReviewCell stress & chaperones2025

Hsp90: Bringing it all together.

Georgios Ioannis Karras, Giorgio Colombo, Andrea N Kravats

Abstract readReview
In one paragraph

Review in Cell stress & chaperones, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

3 authors.

Georgios Ioannis KarrasDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston 77030, TX, USA; Genetics and Epigenetics Graduate Program, The University of Texas MD Anderson Cancer Center, UTHealth Houston Graduate School of Biomedical Sciences, Houston 77030, TX, USA. Electronic address: gkarras@mdanderson.org.
Giorgio ColomboDepartment of Chemistry, University of Pavia, Pavia, Italy. Electronic address: g.colombo@unipv.it.
Andrea N KravatsDepartment of Chemistry and Biochemistry, Miami University, Oxford 45056, OH, USA. Electronic address: kravatan@miamioh.edu.

Funding

Elucidating the Mechanistic Details of the Grp94 Molecular Chaperone through an Integrated Computational and Experimental ApproachR35GM146963 · NIGMS · MIAMI UNIVERSITY OXFORD · PI Andrea N Kravats · 2022 to 2026
$1.7M
Proteotoxic Metabolites in Genome Instability and DiseaseR01CA295874 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Georgios Karras · 2025 to 2026
$1.1M
NCI NIH HHS R01 CA295874NIGMS NIH HHS R35 GM146963
6 · The paper itself

Abstract

Heat-shock protein 90 (Hsp90) is an ancient and multifaceted protein-folding machine essential for most organisms. The past 40 years have uncovered remarkable complexity in the regulation and function of Hsp90, which dwarfs most other machines in the cell in sophistication. Here, we propose four analogies to illustrate Hsp90's sophistication: a multifunctional Swiss Army knife, an automobile engine and its controls, a switchboard acting as a hub and directing signals, and an orchestra conductor setting the tempo of a symphony. Although each of these analogies represents some key Hsp90 activities, none of them captures the entirety of Hsp90's complexity. Together, these roles enable Hsp90 to support both homeostasis and differentiation, both cellular stability and adaptability. At the 11th International Conference on the Hsp90 Chaperone Machine, the consensus was that to understand this major guardian of proteostasis, we need to study how the many facets of Hsp90's function influence each other. We hope that these analogies will help to conceptually integrate the many roles of Hsp90 in proteostasis and help the field develop the practical applications of Hsp90 modulators.

Indexed as

HSP90 Heat-Shock ProteinsAnimalsCongresses as TopicHumansProtein FoldingProteostasisHSP90 Heat-Shock ProteinsEvolutionHsp90ModulatorsProteostasisStructure-function

Identifiers

PMID39889818
PMCPMC12013134

What OpenQuestion holds

Textmetadata
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.