HSP90 Heat-Shock Proteins
"HSP90 Heat-Shock Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A class of MOLECULAR CHAPERONES whose members act in the mechanism of SIGNAL TRANSDUCTION by STEROID RECEPTORS.
Descriptor ID |
D018841
|
MeSH Number(s) |
D12.776.580.216.380
|
Concept/Terms |
HSP90 Heat-Shock Proteins- HSP90 Heat-Shock Proteins
- HSP90 Heat Shock Proteins
- Heat-Shock Proteins, HSP90
- Heat-Shock Proteins 90
- Heat Shock Proteins 90
|
Below are MeSH descriptors whose meaning is more general than "HSP90 Heat-Shock Proteins".
Below are MeSH descriptors whose meaning is more specific than "HSP90 Heat-Shock Proteins".
This graph shows the total number of publications written about "HSP90 Heat-Shock Proteins" by people in this website by year, and whether "HSP90 Heat-Shock Proteins" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 0 | 2 | 2 |
1998 | 0 | 1 | 1 |
1999 | 1 | 0 | 1 |
2001 | 1 | 1 | 2 |
2004 | 2 | 1 | 3 |
2005 | 4 | 4 | 8 |
2006 | 5 | 2 | 7 |
2007 | 4 | 1 | 5 |
2008 | 3 | 2 | 5 |
2009 | 4 | 3 | 7 |
2010 | 5 | 2 | 7 |
2011 | 5 | 3 | 8 |
2012 | 5 | 3 | 8 |
2013 | 5 | 2 | 7 |
2014 | 2 | 5 | 7 |
2015 | 2 | 2 | 4 |
2016 | 6 | 1 | 7 |
2017 | 5 | 0 | 5 |
2018 | 0 | 1 | 1 |
2019 | 1 | 2 | 3 |
2020 | 4 | 1 | 5 |
2021 | 1 | 0 | 1 |
2022 | 0 | 1 | 1 |
2024 | 2 | 1 | 3 |
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Below are the most recent publications written about "HSP90 Heat-Shock Proteins" by people in Profiles.
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HSP90 inhibitor AUY922 suppresses tumor growth and modulates immune response through YAP1-TEAD pathway inhibition in gastric cancer. Cancer Lett. 2025 Feb 01; 610:217354.
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Selection for robust metabolism in domesticated yeasts is driven by adaptation to Hsp90 stress. Science. 2024 Jul 26; 385(6707):eadi3048.
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Protein-folding chaperones predict structure-function relationships and cancer risk in BRCA1 mutation carriers. Cell Rep. 2024 Feb 27; 43(2):113803.
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Metabolic targeting of NRF2 potentiates the efficacy of the TRAP1 inhibitor G-TPP through reduction of ROS detoxification in colorectal cancer. Cancer Lett. 2022 11 28; 549:215915.
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Disruption of DNA Repair and Survival Pathways through Heat Shock Protein Inhibition by Onalespib to Sensitize Malignant Gliomas to Chemoradiation Therapy. Clin Cancer Res. 2022 05 02; 28(9):1979-1990.
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HSP90-CDC37 functions as a chaperone for the oncogenic FGFR3-TACC3 fusion. Mol Ther. 2022 04 06; 30(4):1610-1627.
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Inhibition of heat shock protein 90 destabilizes receptor tyrosine kinase ROR1 in lung adenocarcinoma. Cancer Sci. 2021 Mar; 112(3):1225-1234.
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Loss of ARID1A Promotes Epithelial-Mesenchymal Transition and Sensitizes Pancreatic Tumors to Proteotoxic Stress. Cancer Res. 2021 01 15; 81(2):332-343.
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Intravenous Immunoglobulin G Suppresses Heat Shock Protein (HSP)-70 Expression and Enhances the Activity of HSP90 and Proteasome Inhibitors. Front Immunol. 2020; 11:1816.
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Exome Sequencing in Individuals with Isolated Biliary Atresia. Sci Rep. 2020 02 17; 10(1):2709.