Hypoxia-reoxygenation increase invasiveness of PANC-1 cells through Rac1/MMP-2

被引:31
作者
Binker, Marcelo G. [1 ,2 ]
Binker-Cosen, Andres A. [1 ]
Richards, Daniel [1 ]
Gaisano, Herbert Y. [2 ]
de Cosen, Rodica H. [1 ]
Cosen-Binker, Laura I. [1 ,2 ]
机构
[1] CBRHC Res Ctr, RA-1426 Buenos Aires, DF, Argentina
[2] Univ Toronto, Dept Physiol & Med, Toronto, ON, Canada
关键词
Hypoxia-reoxygenation; PANC-1; cells; Rac1; Reactive oxygen species (ROS); Matrix metalloproteinase-2 (MMP-2); Cancer invasion; ISCHEMIA-REPERFUSION; PANCREATIC-CANCER; MATRIX METALLOPROTEINASE-2; MMP-2; ACTIVATION; GTPASE PROTECTS; RAC1; GTPASE; INVASION; LIVER; INHIBITION; INJURY;
D O I
10.1016/j.bbrc.2010.01.125
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
Pancreatic cancer is an aggressive malignancy with proclivity to early metastasis. High expression and activation of the collagenase matrix metalloproteinase-2 (MMP-2) have been found in human pancreatic cancer tissues, being these increased levels of active MMP-2 correlated to tumor invasion and metastasis. Hypoxia and reoxygenation (H-R) are critical pathophysiological conditions during ischemia-reperfusion injury, which has been shown to enhance both invasion and metastasis. In the present study, we investigated the effects of H-R on MMP-2 levels and the invasiveness properties of human pancreatic cancer cells PANC-1. Using specific inhibitors, we found that H-R treatment of these tumor cells induced secretion and activation of MMP-2, which was required for H-R-stimulated basement membrane degradation and cell invasion. Our results also indicate that signaling events involved in H-R-enhanced PANC-1 invasiveness comprehend PI3K-dependent activation of Rac1, which mediated the formation of NADPH-generated reactive oxygen species responsible for MMP-2 secretion and activation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:371 / 376
页数:6
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