Literature DB >> 17317842

Docetaxel-induced apoptosis of human melanoma is mediated by activation of c-Jun NH2-terminal kinase and inhibited by the mitogen-activated protein kinase extracellular signal-regulated kinase 1/2 pathway.

Nizar M Mhaidat1, Xu Dong Zhang, Chen Chen Jiang, Peter Hersey.   

Abstract

PURPOSE: Our studies have shown variable sensitivity of cultured melanoma cells to docetaxel. To better understand this response, we studied the role of signal transduction pathways in modulating docetaxel-induced melanoma killing. EXPERIMENTAL
DESIGN: Involvement of c-Jun NH(2)-terminal kinase (JNK), extracellular signal-regulated kinase 1/2 (ERK1/2), p38 mitogen-activated protein kinase, and Akt signaling was studied by evaluating their extent of activation in melanoma cells after treatment with docetaxel. The effect of their activation on docetaxel-induced apoptosis was assessed using biochemical inhibitors of the pathways and Western blot analysis of proteins involved.
RESULTS: Docetaxel induced activation of both JNK and ERK1/2 but not p38 mitogen-activated protein kinase or Akt kinases. Apoptosis was dependent on activation of JNK and mediated through activation of caspase-2 and caspase-dependent changes in Bax and Bak. The levels of activated JNK in individual lines showed a close correlation with the levels of apoptosis. In contrast, activation of ERK1/2 by docetaxel inhibited apoptosis and the levels of activation in individual lines were inversely correlated to the degree of apoptosis. Studies on the Bcl-2 family proteins seemed to reflect changes induced by activation of JNK and ERK1/2 pathways. Docetaxel-induced JNK activation was required for Bcl-2 phosphorylation as well as caspase-2-dependent activation of Bax and Bak and subsequent mitochondrial release of apoptosis-inducing factor and cytochrome c. In contrast, activation of ERK1/2 resulted in degradation of BH3-only protein Bim and phosphorylation of Bad.
CONCLUSIONS: These studies provide further insights into sensitivity of melanoma cells to taxanes and provide a basis for the current rationale of combining taxanes with inhibitors of the Raf-ERK1/2 pathway.

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Year:  2007        PMID: 17317842     DOI: 10.1158/1078-0432.CCR-06-2216

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  23 in total

1.  GRP78 regulates sensitivity of human colorectal cancer cells to DNA targeting agents.

Authors:  Nizar M Mhaidat; Karem H Alzoubi; Omar F Khabour; Mohammed N Banihani; Qosay A Al-Balas; Sulaiman Swaidan
Journal:  Cytotechnology       Date:  2014-11-16       Impact factor: 2.058

2.  ID1 enhances docetaxel cytotoxicity in prostate cancer cells through inhibition of p21.

Authors:  Hao Geng; Brooks L Rademacher; Janet Pittsenbarger; Chung-Ying Huang; Christopher T Harvey; Marie C Lafortune; Anne Myrthue; Mark Garzotto; Peter S Nelson; Tomasz M Beer; David Z Qian
Journal:  Cancer Res       Date:  2010-04-13       Impact factor: 12.701

3.  A Micro/Nano Composite for Combination Treatment of Melanoma Lung Metastasis.

Authors:  Yu Mi; Chaofeng Mu; Joy Wolfram; Zaian Deng; Tony Ye Hu; Xuewu Liu; Elvin Blanco; Haifa Shen; Mauro Ferrari
Journal:  Adv Healthc Mater       Date:  2016-02-18       Impact factor: 9.933

4.  Malate dehydrogenase 2 confers docetaxel resistance via regulations of JNK signaling and oxidative metabolism.

Authors:  Qiong Liu; Chris T Harvey; Hao Geng; Changhui Xue; Vivian Chen; Tomasz M Beer; David Z Qian
Journal:  Prostate       Date:  2013-02-06       Impact factor: 4.104

5.  Estradiol induces JNK-dependent apoptosis in glioblastoma cells.

Authors:  Nedret Altiok; Melike Ersoz; Meral Koyuturk
Journal:  Oncol Lett       Date:  2011-08-17       Impact factor: 2.967

6.  CCL2 is induced by chemotherapy and protects prostate cancer cells from docetaxel-induced cytotoxicity.

Authors:  David Z Qian; Brooks L S Rademacher; Janet Pittsenbarger; Chung-Ying Huang; Anne Myrthue; Celestia S Higano; Mark Garzotto; Peter S Nelson; Tomasz M Beer
Journal:  Prostate       Date:  2010-03-01       Impact factor: 4.104

7.  Evidence that mitotic exit is a better cancer therapeutic target than spindle assembly.

Authors:  Hsiao-Chun Huang; Jue Shi; James D Orth; Timothy J Mitchison
Journal:  Cancer Cell       Date:  2009-10-06       Impact factor: 31.743

8.  Human melanoma cells under endoplasmic reticulum stress acquire resistance to microtubule-targeting drugs through XBP-1-mediated activation of Akt.

Authors:  Chen Chen Jiang; Fan Yang; Rick F Thorne; Bi Ke Zhu; Peter Hersey; Xu Dong Zhang
Journal:  Neoplasia       Date:  2009-05       Impact factor: 5.715

Review 9.  Small molecules and targeted therapies in distant metastatic disease.

Authors:  P Hersey; L Bastholt; V Chiarion-Sileni; G Cinat; R Dummer; A M M Eggermont; E Espinosa; A Hauschild; I Quirt; C Robert; D Schadendorf
Journal:  Ann Oncol       Date:  2009-08       Impact factor: 32.976

10.  QLT0267, a small molecule inhibitor targeting integrin-linked kinase (ILK), and docetaxel can combine to produce synergistic interactions linked to enhanced cytotoxicity, reductions in P-AKT levels, altered F-actin architecture and improved treatment outcomes in an orthotopic breast cancer model.

Authors:  Jessica Kalra; Corinna Warburton; Karen Fang; Lincoln Edwards; Tim Daynard; Dawn Waterhouse; Wieslawa Dragowska; Brent W Sutherland; Shoukat Dedhar; Karen Gelmon; Marcel Bally
Journal:  Breast Cancer Res       Date:  2009-05-01       Impact factor: 6.466

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