The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.
Rethinking HSF1 in Stress, Development, and Organismal Health
Open accessAbstract
The heat shock response (HSR) was originally discovered as a transcriptional response to elevated temperature shock and led to the identification of heat shock proteins and Heat Shock Factor 1 (HSF1). Since then, HSF1 has been shown to be important for combating other forms of environmental perturbations as well as genetic variations that cause proteotoxic stress. The HSR has long been thought to be an absolute response to conditions of cell stress and the primary mechanism by which HSF1 promotes organismal health by preventing protein aggregation and subsequent proteome imbalance. Accumulating evidence now shows that HSF1, the central player in the HSR, is regulated according to specific cellular requirements through cell-autonomous and non-autonomous signals, and directs transcriptional programs distinct from the HSR during development and in carcinogenesis. Here, we discuss these ‘non-canonical’ roles of HSF1, and its regulation in diverse conditions of development, reproduction, metabolism, and aging, and posit that HSF1 serves to integrate diverse biological and pathological responses.
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Cites
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Heat Shock Proteins: Agents of Cancer Development and Therapeutic Targets in Anti-Cancer Therapy
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Metadata
- Authors
- Li, J., Labbadia, J., & Morimoto, R. I.
- Venue
- Trends in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2017-12
- Volume
- 27
- Issue
- 12
- Pages
- 895-905
- ISSN
- 0962-8924 (ISSN-L)
- OpenAlex
- W2751896753
- Cited by
- 267
- References
- 65
- FWCI
- 1.95
- Type
- journal article
- Language
- en
- Open access
- green
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