Hyperthermia inhibits cell proliferation and induces apoptosis: Relative signaling status of p53, S100A4, and notch in heat sensitive and resistant cell lines

被引:23
作者
Basile, Antonio [2 ]
Biziato, Daniela [2 ]
Sherbet, Gajanan V. [1 ,3 ]
Comi, Paola [2 ]
Cajone, Francesco [2 ]
机构
[1] Univ Newcastle Upon Tyne, Sch Elect Elect & Comp Engn, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Milan, Dept Biomed Sci & Technol, I-20133 Milan, Italy
[3] Inst Mol Med, Huntington Beach, CA USA
关键词
apoptosis; cell proliferation; heat resistance; hyperthermia; notch; P53; S100A4; transient heat exposure;
D O I
10.1002/jcb.21401
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of hyperthermia on the expression of 1353, the apoptosis-associated genes Bax and Bcl-2, Notch and S100A4 have been studied in the HepG2 cell line and the HUT cell line derived from HepG2, adapted for growth in hyperthermic conditions. Hyperthermia inhibits cell proliferation and induces apoptosis. HepG2 and HUT cells differed in respect of anchorage to growth surface, degree of proliferation and apoptosis and expression of 1353, Bax, Bcl-2, Notch, and S100A4 genes. The induction of apoptosis and the inhibition of cell proliferation occurred independently of 1353, and independently also of involvement of the apoptosis family genes Bax and Bcl-2. We demonstrate novel and marked differences between transient heat shock and heat adaptation in respect of pathways of signaling and generation of phenotypic effects in vitro. Different signaling patterns have been identified here. Pathways of signaling by S100A4, by its interaction with and sequestration of 1353, and by Notch also seem differentially operational in the induction of apoptosis, and both appear to be activated as alternative pathways in the context of hyperthermia signaling independently of p53.
引用
收藏
页码:212 / 220
页数:9
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