Literature DB >> 7594802

Heat shock proteins, thermotolerance, and their relevance to clinical hyperthermia.

G C Li1, N F Mivechi, G Weitzel.   

Abstract

Mammalian cells, when exposed to a non-lethal heat shock, have the ability to acquire a transient resistance to subsequent exposures at elevated temperatures, a phenomenon termed thermotolerance. The mechanism(s) for the development of thermotolerance is not well understood, but earlier experimental evidence suggests that protein synthesis may play a role in its manifestation. On the molecular level, heat shock activates a specific set of genes, so-called heat shock genes, and results in the preferential synthesis of heat shock proteins. The heat shock response, specifically the regulation, expression and functions of heat shock proteins, has been extensively studied in the past decades and has attracted the attention of a wide spectrum of investigators ranging from molecular and cell biologists to radiation and hyperthermia oncologists. There is much data supporting the hypothesis that heat shock proteins play important roles in modulating cellular responses to heat shock, and are involved in the development of thermotolerance. This review summarizes some current knowledge on thermotolerance and the functions of heat shock proteins, especially hsp70. The relationship between thermotolerance development and hsp70 synthesis in tumours and in normal tissues is examined. The possibility of using hsp70 as an indicator for thermotolerance is discussed.

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Year:  1995        PMID: 7594802     DOI: 10.3109/02656739509022483

Source DB:  PubMed          Journal:  Int J Hyperthermia        ISSN: 0265-6736            Impact factor:   3.914


  39 in total

1.  Kadota Fund International Forum 2004. Application of thermal stress for the improvement of health, 15-18 June 2004, Awaji Yumebutai International Conference Center, Awaji Island, Hyogo, Japan. Final report.

Authors:  Tsutomu Sugahara; J van der Zee; Harm H Kampinga; Zeliko Vujaskovic; Motoharu Kondo; Takeo Ohnishi; Gloria Li; Heon J Park; Dennis B Leeper; Valentina Ostapenko; Elizabeth A Repasky; Masami Watanabe; Chang W Song
Journal:  Int J Hyperthermia       Date:  2008-03       Impact factor: 3.914

2.  Heat shock proteins and Bcl-2 expression and function in relation to the differential hyperthermic sensitivity between leukemic and normal hematopoietic cells.

Authors:  R Setroikromo; P K Wierenga; M A W H van Waarde; J F Brunsting; E Vellenga; H H Kampinga
Journal:  Cell Stress Chaperones       Date:  2007       Impact factor: 3.667

Review 3.  Protein misfolding, aggregation, and autophagy after brain ischemia.

Authors:  Tianfei Luo; Yujung Park; Xin Sun; Chunli Liu; Bingren Hu
Journal:  Transl Stroke Res       Date:  2013-11-09       Impact factor: 6.829

Review 4.  Prions in yeast.

Authors:  Susan W Liebman; Yury O Chernoff
Journal:  Genetics       Date:  2012-08       Impact factor: 4.562

5.  Hsp72 functions as a natural inhibitory protein of c-Jun N-terminal kinase.

Authors:  H S Park; J S Lee; S H Huh; J S Seo; E J Choi
Journal:  EMBO J       Date:  2001-02-01       Impact factor: 11.598

6.  Irreversible aggregation of protein synthesis machinery after focal brain ischemia.

Authors:  F Zhang; C L Liu; B R Hu
Journal:  J Neurochem       Date:  2006-07       Impact factor: 5.372

7.  Chronic heat treatment positively impacts metabolic profile of ovariectomized rats: association with heat shock response pathways.

Authors:  Yana Picinin Sandri Lissarassa; Carolain Felipin Vincensi; Lílian Corrêa Costa-Beber; Analú Bender Dos Santos; Pauline Brendler Goettems-Fiorin; Jaíne Borges Dos Santos; Yohanna Hannnah Donato; Guilherme Wildner; Paulo Ivo Homem de Bittencourt Júnior; Matias Nunes Frizzo; Thiago Gomes Heck; Mirna Stela Ludwig
Journal:  Cell Stress Chaperones       Date:  2020-03-25       Impact factor: 3.667

8.  Expression of heat-shock protein 70 (Hsp70) in the respiratory tract and lungs of fire victims.

Authors:  S Marschall; M A Rothschild; M Bohnert
Journal:  Int J Legal Med       Date:  2006-05-31       Impact factor: 2.686

9.  Expression of inducible Hsp70 enhances the proliferation of MCF-7 breast cancer cells and protects against the cytotoxic effects of hyperthermia.

Authors:  J A Barnes; D J Dix; B W Collins; C Luft; J W Allen
Journal:  Cell Stress Chaperones       Date:  2001-10       Impact factor: 3.667

10.  Spatial analysis of cell death and Hsp70 induction in brain, thymus, and bone marrow of the hyperthermic rat.

Authors:  Hiwote T Belay; Ian R Brown
Journal:  Cell Stress Chaperones       Date:  2003       Impact factor: 3.667

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