期刊
EXPERIMENTAL CELL RESEARCH
卷 317, 期 17, 页码 2479-2489出版社
ELSEVIER INC
DOI: 10.1016/j.yexcr.2011.07.012
关键词
Cancer; Stress; Survival
资金
- MIUR [1558]
- Italian Ministry of Health [0000118]
The translationally controlled tumor protein (TCTP) displays growth-promoting and antiapoptotic properties. To gain information on the role of TCTP in cancer disease, we studied the modulation of TCTP and cell survival under stress conditions on tumor cell lines of different origins. When cancer cells were exposed to a mild oxidative stress, such low doses of Arsenic trioxide (ATO) or hydrogen peroxide (H2O2), up-regulation of TCTP was observed in cells survived to the treatment. Differently, a strong oxidative hit provided by ATO combined with glutathione (GSH) depletion or condition of glucose deprivation caused a down-modulation of TCTP followed by cell death. Clones with a forced expression of TCTP or with silenced TCTP were obtained from the breast cancer cell line MDA-MB-231. The sensitivity to oxidative stress was strongly enhanced in down-modulated TCTP cells while decreasing in cells with high levels of TCTP. Together these results indicate that TCTP is a survival factor that protects cancer cells from oxidative stress-induced cell-death. We propose TCTP as a stress hallmark that may be exploited as a therapeutic target to decrease the resistance of cancer cells to anticancer therapy. (C) 2011 Elsevier Inc. All rights reserved.
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