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DAPK-HSF1 interaction as a new positive feedback loop for TNF-induced apoptosis in colorectal cancer cells
Author(s) -
Natalya Benderska,
Jelena Ivanovska,
Tilman T. Rau,
Jan SchulzeLuehrmann,
Suma Mohan,
Saritha Chakilam,
Muktheshwar Gandesiri,
Elisabeth Ziesché,
Thomas Fischer,
Stephan Söder,
Abbas Agaimy,
Luitpold Distel,
Heinrich Sticht,
Vijayalakshmi Mahadevan,
Regine SchneiderStock
Publication year - 2014
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.157024
Subject(s) - hsf1 , biology , gene knockdown , cancer research , colorectal cancer , apoptosis , protein kinase a , tumor necrosis factor alpha , phosphorylation , kinase , heat shock protein , cancer , microbiology and biotechnology , immunology , gene , biochemistry , genetics , hsp70
Death-associated protein kinase (DAPK) is a serine-threonine kinase with tumor suppressor function. Previously we demonstrated that TNF induced DAPK-mediated apoptosis in colorectal cancer. However the protein-protein interaction network associated with TNF-DAPK signaling still remains unclear. We identified HSF1 as a new DAPK phosphorylation target in response to low concentration of TNF and verified a physical interaction between DAPK and HSF1 both in vitro and in vivo. We show that HSF1 binds to the DAPK promoter. Transient over-expression of HSF1 protein led to an increase in DAPK mRNA level and consequently to an enforcement of apoptosis. In contrast, treatment with a DAPK specific inhibitor as well as DAPKsh knockdown abolished the activation of HSF1 at Ser230. Furthermore, translational studies demonstrated a positive correlation between DAPK and pHSF1S230 protein expression in human colorectal carcinoma tissues. Together, our data define a novel link between DAPK and HSF1 and highlight a positive feedback loop in DAPK regulation under mild inflammatory stress in colorectal tumors. For the first time we show that under TNF the pro-survival HSF1 protein can be redirected to a pro-apoptotic program.

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