Tyrosine phosphatase inhibitors combined with retinoic acid can enhance differentiation of neuroblastoma cells and trigger ERK- and AKT-dependent, p53-independent senescence (Publication with Expression of Concern)

被引:30
作者
Clark, Owen [1 ]
Daga, Shruti [1 ]
Stoker, Andrew W. [1 ]
机构
[1] UCL, Inst Child Hlth, Neural Dev Unit, London WC1N 1EH, England
关键词
Neuroblastoma; p53; Senescence; Vanadium; PTEN; Tyrosine phosphatase; PREMATURE SENESCENCE; CELLULAR SENESCENCE; PHOSPHATIDYLINOSITOL; 3-KINASE; NEUROTROPHIC FACTOR; SH-SY5Y CELLS; CYCLE ARREST; CANCER; THERAPY; PROTEIN; P53;
D O I
10.1016/j.canlet.2012.09.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Retinoic acid (RA)-induced differentiation therapy is partially successful in neuroblastoma treatment. We found that a novel combination of vanadium-based PTP inhibitors with RA induced extensive differentiation in neuroblastoma cells. In contrast to RA alone, this led to either permanent differentiation or senescence after 14 days of combined treatment followed by chemical removal. Senescence was dependent in part on synergistic ART and ERR activation. p21 was also strongly induced, but in contrast to oncogene-induced senescence, p53 was not activated. Vanadium-based inhibitors thus serve strongly to enhance RA's ability to drive differentiation and a novel form of senescence in neuroblastoma cells. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:44 / 54
页数:11
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