ZAK is required for doxorubicin, a novel ribotoxic stressor, to induce SAPK activation and apoptosis in HaCaT cells

Kristin A D Sauter, Eli A. Magun, Mihail S. Iordanov, Bruce E. Magun

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Doxorubicin is an anthracycline drug that is one of the most effective and widely used anticancer agents for the treatment of both hematologic and solid tumors. The stress-activated protein kinases (sapKs) are frequently activated by a number of cancer chemotherapeutics. When phosphorylated, the sapKs initiate a cascade that leads to the production of proinflammatory cytokines. some inhibitors of protein synthesis, known as ribotoxic stressors, coordinately activate sapKs and lead to apoptotic cell death. We demonstrate that doxorubicin effectively inhibits protein synthesis, activates sapKs, and causes apoptosis. Ribotoxic stressors share a common mechanism in that they require ZaK, an upstream Map3K, to activate the pro-apoptotic and proinflammatory signaling pathways that lie downstream of sapKs. By employing siRNa mediated knockdown of ZaK or administration of sorafenib and nilotinib, kinase inhibitors that have a high affi nity for ZaK, we provide evidence that ZaK is required for doxorubicin-induced proinflammatory and apoptotic responses in haCaT cells, a pseudo-normal keratinocyte cell line, but not in heLa cells, a cancerous cell line. ZaK has two different isoforms, ZaK-α (91 kDa) and ZaK-β (51 kDa). haCaT or heLa cells treated with doxorubicin and immunoblotted for ZAK displayed a progressive decrease in the ZAK-α band and the appearance of ZAK-β bands of larger size. abrogation of these changes after exposure of cells to sorafenib and nilotinib suggests that these alterations occur following stimulation of ZaK. We suggest that ZaK inhibitors such as sorafenib or nilotinib may be effective when combined with doxorubicin to treat cancer patients.

Original languageEnglish (US)
Pages (from-to)258-266
Number of pages9
JournalCancer Biology and Therapy
Volume10
Issue number3
StatePublished - Aug 1 2010

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Heat-Shock Proteins
Doxorubicin
Protein Kinases
Apoptosis
HeLa Cells
Cell Line
Neoplasms
Protein Synthesis Inhibitors
Anthracyclines
Keratinocytes
Antineoplastic Agents
Protein Isoforms
Cell Death
Phosphotransferases
Cytokines
Pharmaceutical Preparations
4-methyl-N-(3-(4-methylimidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-((4-pyridin-3-ylpyrimidin-2-yl)amino)benzamide
sorafenib
Proteins
Therapeutics

Keywords

  • Apoptosis
  • Doxorubicin
  • Ribotoxic stressor
  • SAPKs
  • ZAK

ASJC Scopus subject areas

  • Cancer Research
  • Oncology
  • Molecular Medicine
  • Pharmacology

Cite this

ZAK is required for doxorubicin, a novel ribotoxic stressor, to induce SAPK activation and apoptosis in HaCaT cells. / Sauter, Kristin A D; Magun, Eli A.; Iordanov, Mihail S.; Magun, Bruce E.

In: Cancer Biology and Therapy, Vol. 10, No. 3, 01.08.2010, p. 258-266.

Research output: Contribution to journalArticle

Sauter, Kristin A D ; Magun, Eli A. ; Iordanov, Mihail S. ; Magun, Bruce E. / ZAK is required for doxorubicin, a novel ribotoxic stressor, to induce SAPK activation and apoptosis in HaCaT cells. In: Cancer Biology and Therapy. 2010 ; Vol. 10, No. 3. pp. 258-266.
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