Hypoxia and the presence of human vascular endothelial cells affect prostate cancer cell invasion and metabolism

被引:30
作者
Ackerstaff, Ellen
Artemov, Dmitri
Gillies, Robert J.
Bhujwalla, Zaver M.
机构
[1] Johns Hopkins Univ, Sch Med, Dept Radiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Dept Oncol, Baltimore, MD 21205 USA
[4] Univ Arizona, Arizona Canc Ctr, Dept Biochem & Mol Biophys, Tucson, AZ 85724 USA
来源
NEOPLASIA | 2007年 / 9卷 / 12期
关键词
prostate cancer; hypoxia; invasion; endothelial/cancer cell interaction; magnetic resonance (MR) imaging and spectroscopy;
D O I
10.1593/neo.07568
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor progression and metastasis are influenced by hypoxia, as well as by interactions between cancer cells and components of the stroma, such as endothelial cells. Here, we have used a magnetic resonance (MR) compatible invasion assay to further understand the effects of hypoxia on human prostate cancer cell invasion and metabolism in the presence and absence of human umbilical vein endothelial cells (HUVECs). Additionally, we compared endogenous activities of selected proteases related to invasion in PC-3 cells and HUVECs, profiled gene expression of PC-3 cells by microarray, and evaluated cell proliferation of PC-3 cells and HUVECs by flow cytometry, under hypoxic and oxygenated conditions. The invasion of less-invasive DU-145 cells was not affected by either hypoxia or the presence of HUVECs. However, hypoxia significantly decreased the invasion of PC-3 cells. This hypoxia-induced decrease was attenuated by the presence of HUVECs, whereas under oxygenated conditions, HUVECs did not alter the invasion of PC-3 cells. Cell metabolism changed distinctly with hypoxia and invasion. The endogenous activity of selected extracellular proteases, although altered by hypoxia, did not fully explain the hypoxia-induced changes in invasion. Gene expression profiling indicated that hypoxia affects multiple cellular functions and pathways.
引用
收藏
页码:1138 / 1151
页数:14
相关论文
共 52 条
[21]   Hypoxia increases heparanase-dependent tumor cell invasion, which can be inhibited by antiheparanase antibodies [J].
He, XT ;
Brenchley, PEC ;
Jayson, GC ;
Hampson, L ;
Davies, J ;
Hampson, IN .
CANCER RESEARCH, 2004, 64 (11) :3928-3933
[22]  
HEWETT PW, 1993, IN VITRO CELL DEV-AN, V29A, P823
[23]   Extracellular matrix composition and hypoxia regulate the expression of HLA-G and integrins in a human trophoblast cell line [J].
Kilburn, BA ;
Wang, J ;
Duniec-Dmuchkowski, ZM ;
Leach, RE ;
Romero, R ;
Armant, DR .
BIOLOGY OF REPRODUCTION, 2000, 62 (03) :739-747
[24]  
Krishnamachary B, 2003, CANCER RES, V63, P1138
[25]  
Krtolica A, 1996, CANCER RES, V56, P1168
[26]   Inhibition of endothelial cell differentiation on a glycosylated reconstituted basement membrane complex [J].
Kuzuya, M ;
Satake, S ;
Miura, H ;
Hayashi, T ;
Iguchi, A .
EXPERIMENTAL CELL RESEARCH, 1996, 226 (02) :336-345
[27]   The microenvironment of the tumour-host interface [J].
Liotta, LA ;
Kohn, EC .
NATURE, 2001, 411 (6835) :375-379
[28]   Molecular and cellular regulation of glucose transporter (GLUT) proteins in cancer [J].
Macheda, ML ;
Rogers, S ;
Best, JD .
JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 202 (03) :654-662
[29]  
Mori Noriko, 2003, Mol Imaging, V2, P124, DOI 10.1162/153535003322332000
[30]   Requirement of cyclooxygenase-2 expression and prostaglandins for human prostate cancer cell invasion [J].
Nithipatikom, K ;
Isbell, MA ;
Lindholm, PF ;
Kajdacsy-Balla, A ;
Kaul, S ;
Campell, WB .
CLINICAL & EXPERIMENTAL METASTASIS, 2002, 19 (07) :593-601