Literature DB >> 16288745

Ha-Ras sensitizes transformed mouse skin cells to Anisomycin-induced apoptosis.

Juan F Santibañez1, Claudia Hurtado.   

Abstract

Efforts have been made to develop a chemoprevention that selectively triggers apoptosis in malignant cancer cells. Here, we demonstrated that a mutated Ha-Ras activity is required in Anisomycin-induced apoptosis in transformed keratinocytes. Anisomycin stimulates JNK activity and apoptosis in oncogenic Ha-Ras positive cells, but not in normal keratinocytes. This effect was demonstrated in stably transfected cells with dominant negative Ha-Ras, that protected transformed cells, and oncogenic Ha-Ras that sensitized non-transformed cells to Anisomycin-induced apoptosis. Lastly, the treatment of cells with inhibitors of the JNK displayed resistance to Anisomycin induced apoptosis. These data suggests that the oncogenic Ha-Ras is important for Anisomycin-induced JNK activation and apoptosis in transformed keratinocytes.

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Year:  2005        PMID: 16288745     DOI: 10.1016/j.febslet.2005.10.025

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  5 in total

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4.  microRNA let-7c is essential for the anisomycin-elicited apoptosis in Jurkat T cells by linking JNK1/2 to AP-1/STAT1/STAT3 signaling.

Authors:  Zhiwei Zhou; Xijian Lu; Jin Wang; Jia Xiao; Jing Liu; Feiyue Xing
Journal:  Sci Rep       Date:  2016-04-18       Impact factor: 4.379

5.  Functional and prognostic significance of long non-coding RNA MALAT1 as a metastasis driver in ER negative lymph node negative breast cancer.

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Journal:  Oncotarget       Date:  2016-06-28
  5 in total

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