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Ha-rasval12 induces HSP70b transcription via the HSE/HSF1 system, but HSP70b expression is suppressed in Ha-rasval12-transformed cells.

Authors :
Stanhill, A.
Levin, V.
Hendel, A.
Shachar, I.
Kazanov, D.
Arber, N.
Kaminski, N.
Engelberg, D.
Source :
Oncogene; 3/9/2006, Vol. 25 Issue 10, p1485-1495, 11p, 2 Diagrams, 1 Chart, 8 Graphs
Publication Year :
2006

Abstract

Heat shock proteins (Hsps) are overexpressed in many tumors, but are downregulated in some tumors. To check for a direct effect of Ha-Ras<superscript>val12</superscript> on HSP70 transcription, we transiently expressed the oncoprotein in Rat1 fibroblasts and monitored its effect on HSP70b promoter-driven reporter gene. We show that expression of Ha-Ras<superscript>val12</superscript> induced this promoter. Promoter analysis via systematic deletions and point mutations revealed that Ha-Ras<superscript>val12</superscript> induces HSP70b transcription via heat shock elements (HSEs). Also, Ha-Ras<superscript>val12</superscript> induction of HSE-mediated transcription was dramatically reduced in HSF1−/− cells. Yet, residual effect of Ha-Ras<superscript>val12</superscript> that was still measured in HSF1−/− cells suggests that some of the Ha-Ras<superscript>val12</superscript> effect is Hsf1-independent. When HSF1−/− cells, stably expressing Ha-Ras<superscript>val12</superscript>, were grown on soft agar only small colonies were formed suggesting a role for heat shock factor 1 (Hsf1) in Ha-Ras<superscript>val12</superscript>-mediated transformation. Although Ha-ras<superscript>Val12</superscript> seems to be an inducer of HSP70's expression, we found that in Ha-ras<superscript>Val12-</superscript>transformed fibroblasts expression of this gene is suppressed. This suppression is correlated with higher sensitivity of Ha-ras<superscript>val12</superscript>-transformed cells to heat shock. We suggest that Ha-ras<superscript>Val12</superscript> is involved in Hsf1 activation, thereby inducing the cellular protective response. Cells that repress this response are perhaps those that acquire the capability to further proliferate and become transformed clones.Oncogene (2006) 25, 1485–1495. doi:10.1038/sj.onc.1209193; published online 7 November 2005 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09509232
Volume :
25
Issue :
10
Database :
Complementary Index
Journal :
Oncogene
Publication Type :
Academic Journal
Accession number :
20029144
Full Text :
https://doi.org/10.1038/sj.onc.1209193