Ca2+ pools and cell growth -: Evidence for sarcoendoplasmic Ca2+-ATPases 2B involvement in human prostate cancer cell growth control

被引:75
作者
Legrand, G
Humez, S
Slomianny, C
Dewailly, E
Vanden Abeele, F
Mariot, P
Wuytack, F
Prevarskaya, N
机构
[1] Univ Sci & Tech Lille Flandres Artois, Lab Physiol Cellulaire, INSERM, EPI 9938, F-59655 Villeneuve Dascq, France
[2] Univ Artois, Fac Sci Jean Perrin, F-62300 Lens, France
[3] Catholic Univ Louvain, Dept Mol Cell Biol, Fysiol Lab, B-3000 Louvain, Belgium
关键词
D O I
10.1074/jbc.M107011200
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 present study demonstrates for the first time that intracellular calcium-ATPases and calcium pool content are closely associated with prostate cancer LNCaP cell growth. Cell growth was modulated by changing the amount of epidermal growth factor, serum, and andro-gene in culture media. Using the microspectrofluorimetric method with Fura-2 and Mag Fura-2 as probes, we show that in these cells, the growth rate is correlated with intracellular calcium pool content. Indeed, an increased growth rate is correlated with an increase in the calcium pool filling state, whereas growth-inhibited cells show a reduced calcium pool load. Using Western blotting and immunocytochemistry, we show that endoplasmic reticulum calcium pump expression is closely linked to LNCaP cell growth, and are a common target of physiological stimuli that control cell growth. Moreover, we clearly demonstrate that inhibition of these pumps, using thapsigargin, inhibits LNCaP cell growth and prevents growth factor from stimulating cell proliferation. Our results thus provide evidence for the essential role of functional endoplasmic reticulum calcium pumps and calcium pool in control of prostate cancer LNCaP cell growth, raising the prospect of new targets for the treatment of prostate cancer.
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收藏
页码:47608 / 47614
页数:7
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