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Sci. STKE, 11 December 2007 EDITORS' CHOICETumor Cell Death c-Myc to Melanoma Cells: Drop Dead?John F. Foley Sciences STKE, AAAS, Washington, DC 20005, USA
Because the proteasome regulates the cell cycle and apoptosis, proteasome inhibitor-mediated tumor cell death is not that surprising. What is puzzling, however, given the vital role of the proteasome in protein turnover, is the paucity of side effects on normal cells. What makes protease inhibitors so tumor cell-selective? One such compound, bortezomib, increases the abundance, in cancer cells but not in normal cells, of the mRNA and protein of the proapoptotic factor, NOXA. Nikiforov et al. investigated the mechanism by which bortezomib causes cell death in melanoma cell lines. Western blotting analysis showed that the bortezomib-dependent increase in NOXA abundance in melanoma cells was blocked by the transcriptional inhibitor actinomysin D. Bortezomib still increased the abundance of NOXA in cell lines that were treated with short interfering RNAs specific for those transcription factors known to target NOXA: p53, hypoxia-inducible factor-1 M. A. Nikiforov, M. Riblett, W.-H. Tang, V. Gratchouck, D. Zhuang, Y. Fernandez, M. Verhaegen, S. Varambally, A. M. Chinnaiyan, A. J. Jakubowiak, M. S. Soengas, Tumor cell-selective regulation of NOXA by c-MYC in response to proteasome inhibition. Proc. Natl. Acad. Sci. U.S.A. 104, 19488-19493 (2007). [Abstract] [Full Text]
Citation: J. F. Foley, c-Myc to Melanoma Cells: Drop Dead? Sci. STKE 2007, tw448 (2007). The editors suggest the following Related Resources on Science sites:In Science Signaling
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Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882