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Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat.
Testis cancer cells are more sensitive than bladder and most other cancer cells to chemotherapeutic drugs both in the clinic and in vitro. In this study we show that they are also more sensitive than bladder cancer cells to heat. Since heat and drug sensitivity may be related to the ability of a cel...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033863/ https://www.ncbi.nlm.nih.gov/pubmed/7669571 |
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author | Richards, E. H. Hickman, J. A. Masters, J. R. |
author_facet | Richards, E. H. Hickman, J. A. Masters, J. R. |
author_sort | Richards, E. H. |
collection | PubMed |
description | Testis cancer cells are more sensitive than bladder and most other cancer cells to chemotherapeutic drugs both in the clinic and in vitro. In this study we show that they are also more sensitive than bladder cancer cells to heat. Since heat and drug sensitivity may be related to the ability of a cell to mount a stress response, constitutive and induced levels of heat shock proteins (HSPs) in three testis and three bladder human cancer cell lines were measured using Western blotting and scanning densitometry. No correlation between constitutive levels of HSP 90 or HSP 73/72 and cellular heat sensitivity was found. However, HSP 27 levels were much lower in the testis tumour cells, suggesting that low HSP 27 expression might contribute to heat sensitivity. Protein synthesis studies using [35S]methionine indicated that, for the same heat shocks, the kinetics of synthesis and decay of HSP 90 and HSP 73/72 in 833K (the most heat sensitive testis cells) was similar to or greater than that in HT1376 (the most heat-resistant bladder cells). Both 833K and HT1376 developed thermotolerance, and this followed an increase in synthesis of HSPs. These results indicate that, although there are differences in the constitutive levels of HSPs between testis and bladder cancer cells, both cell types are capable of mounting an induced heat shock response and can develop a similar degree of thermotolerance. IMAGES: |
format | Text |
id | pubmed-2033863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20338632009-09-10 Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. Richards, E. H. Hickman, J. A. Masters, J. R. Br J Cancer Research Article Testis cancer cells are more sensitive than bladder and most other cancer cells to chemotherapeutic drugs both in the clinic and in vitro. In this study we show that they are also more sensitive than bladder cancer cells to heat. Since heat and drug sensitivity may be related to the ability of a cell to mount a stress response, constitutive and induced levels of heat shock proteins (HSPs) in three testis and three bladder human cancer cell lines were measured using Western blotting and scanning densitometry. No correlation between constitutive levels of HSP 90 or HSP 73/72 and cellular heat sensitivity was found. However, HSP 27 levels were much lower in the testis tumour cells, suggesting that low HSP 27 expression might contribute to heat sensitivity. Protein synthesis studies using [35S]methionine indicated that, for the same heat shocks, the kinetics of synthesis and decay of HSP 90 and HSP 73/72 in 833K (the most heat sensitive testis cells) was similar to or greater than that in HT1376 (the most heat-resistant bladder cells). Both 833K and HT1376 developed thermotolerance, and this followed an increase in synthesis of HSPs. These results indicate that, although there are differences in the constitutive levels of HSPs between testis and bladder cancer cells, both cell types are capable of mounting an induced heat shock response and can develop a similar degree of thermotolerance. IMAGES: Nature Publishing Group 1995-09 /pmc/articles/PMC2033863/ /pubmed/7669571 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Richards, E. H. Hickman, J. A. Masters, J. R. Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
title | Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
title_full | Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
title_fullStr | Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
title_full_unstemmed | Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
title_short | Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
title_sort | heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033863/ https://www.ncbi.nlm.nih.gov/pubmed/7669571 |
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