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Heat shock protein expression in testis and bladder cancer cell lines exhibiting differential sensitivity to heat.

作者信息

Richards E H, Hickman J A, Masters J R

机构信息

Institute of Urology and Nephrology, University College London, UK.

出版信息

Br J Cancer. 1995 Sep;72(3):620-6. doi: 10.1038/bjc.1995.383.

DOI:10.1038/bjc.1995.383
PMID:7669571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2033863/
Abstract

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/9fb7db9dc5de/brjcancer00043-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/7d2307d588a7/brjcancer00043-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/adfe4eb41d11/brjcancer00043-0106-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/b5d03ba7f756/brjcancer00043-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/1cd30cb8fdce/brjcancer00043-0107-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/9fb7db9dc5de/brjcancer00043-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/7d2307d588a7/brjcancer00043-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/adfe4eb41d11/brjcancer00043-0106-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/b5d03ba7f756/brjcancer00043-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/1cd30cb8fdce/brjcancer00043-0107-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0941/2033863/9fb7db9dc5de/brjcancer00043-0108-a.jpg

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引用本文的文献

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本文引用的文献

1
Thermotolerance in mammalian cells. Protein denaturation and aggregation, and stress proteins.哺乳动物细胞中的热耐受性。蛋白质变性与聚集以及应激蛋白。
J Cell Sci. 1993 Jan;104 ( Pt 1):11-7. doi: 10.1242/jcs.104.1.11.
2
Induction of Chinese hamster HSP27 gene expression in mouse cells confers resistance to heat shock. HSP27 stabilization of the microfilament organization.中国仓鼠HSP27基因在小鼠细胞中的诱导表达赋予了对热休克的抗性。HSP27对微丝组织的稳定作用。
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Int J Cancer. 1993 Jan 21;53(2):340-6. doi: 10.1002/ijc.2910530228.
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Cancer Res. 1993 Oct 1;53(19):4443-8.
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Correlation between synthesis of heat shock proteins and development of thermotolerance in Chinese hamster fibroblasts.中国仓鼠成纤维细胞中热休克蛋白合成与耐热性发展之间的相关性。
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Established cell line of urinary bladder carcinoma (T24) containing tumour-specific antigen.建立的含有肿瘤特异性抗原的膀胱癌细胞系(T24)。
Int J Cancer. 1973 May;11(3):765-73. doi: 10.1002/ijc.2910110327.
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Tissue culture model of transitional cell carcinoma: characterization of twenty-two human urothelial cell lines.移行细胞癌的组织培养模型:22种人尿路上皮细胞系的特征
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