Expression of hypoxia-inducible factor 1 α in brain tumors -: Association with angiogenesis, invasion, and progression

被引:3
作者
Zagzag, D
Zhong, H
Scalzitti, JM
Laughner, E
Simons, JW
Semenza, GL
机构
[1] NYU, Med Ctr, Dept Pathol, Div Neuropathol, New York, NY 10016 USA
[2] NYU, Med Ctr, Kaplan Canc Ctr, Dept Neurosurg,Microvasc & Mol Neurooncol Lab, New York, NY 10016 USA
[3] Johns Hopkins Univ Hosp, Dept Pharmacol, Johns Hopkins Oncol Ctr, Brady Urol Inst, Baltimore, MD 21287 USA
[4] Univ Nebraska, Dept Biol, Bruner Hall Sci, Kearney, NE USA
[5] Johns Hopkins Univ, Sch Med, Dept Pediat, Inst Med Genet, Baltimore, MD 21205 USA
关键词
angiogenesis; glioma; glioblastoma multiforme; hemangioblastoma; HIF-1; alpha; beta; hypoxia;
D O I
10.1002/1097-0142(20000601)88:11<2606::AID-CNCR25>3.0.CO;2-W
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND, Hypoxia inducible factor-1 (HIF-1) plays a critical role in angiogenesis during vascular development. The authors tested the hypothesis that HIF-1 expression correlates with progression and angiogenesis in brain tumors. METHODS, The authors investigated the expression of the HIF-1 alpha and HIF-1 beta subunits in human glioma cell lines and brain tumor tissues using Western blot analysis and immunohistochemistry. RESULTS. In glioblastomas multiforme (GBMs), HIF-1 alpha primarily was localized in pseudopalisading cells around areas of necrosis and in tumor cells infiltrating the brain at the tumor margin. In contrast, HIF-1 alpha was expressed in stromal cells throughout hemangioblastomas (HBs). Like HIF-1 alpha, HIF-1 beta was most highly expressed in high grade tumors but was expressed more widely than HIF-1 alpha, including cells away from necrotic zones. In the brains of mice injected with Glioma 261 cells, a pattern of HIF-1 alpha expression identical to that observed in human GBMs was noted. CONCLUSIONS. III GBMs, the heterogeneous pattern of HIF-1 alpha expression appears to be determined at least in part by tissue oxygenation, whereas in HBs the homogeneous expression of HIF-1 alpha may be driven by an oncogenic rather than a physiologic stimulus. (C) 2000 American Cancer Society.
引用
收藏
页码:2606 / 2618
页数:13
相关论文
共 67 条
[21]   CLONING OF A FACTOR REQUIRED FOR ACTIVITY OF THE AH (DIOXIN) RECEPTOR [J].
HOFFMAN, EC ;
REYES, H ;
CHU, FF ;
SANDER, F ;
CONLEY, LH ;
BROOKS, BA ;
HANKINSON, O .
SCIENCE, 1991, 252 (5008) :954-958
[22]   Activation of hypoxia-inducible transcription factor depends primarily upon redox-sensitive stabilization of its alpha subunit [J].
Huang, LE ;
Arany, Z ;
Livingston, DM ;
Bunn, HF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32253-32259
[23]   Negative regulation of hypoxia-inducible genes by the von Hippel Lindau protein [J].
Iliopoulos, O ;
Levy, AP ;
Jiang, C ;
Kaelin, WG ;
Goldberg, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :10595-10599
[24]   Cellular and developmental control of O2 homeostasis by hypoxia-inducible factor 1α [J].
Iyer, NV ;
Kotch, LE ;
Agani, F ;
Leung, SW ;
Laughner, E ;
Wenger, RH ;
Gassmann, M ;
Gearhart, JD ;
Lawler, AM ;
Yu, AY ;
Semenza, GL .
GENES & DEVELOPMENT, 1998, 12 (02) :149-162
[25]  
Jiang BH, 1997, CANCER RES, V57, P5328
[26]   Hypoxia-inducible factor 1 levels vary exponentially over a physiologically relevant range of O-2 tension [J].
Jiang, BH ;
Semenza, GL ;
Bauer, C ;
Marti, HH .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (04) :C1172-C1180
[27]   Induces PECAM-1 phosphorylation and transendothelial migration of monocytes [J].
Kalra, VK ;
Shen, Y ;
Sultana, C ;
Rattan, V .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (05) :H2025-H2034
[28]  
KANNO H, 1994, CANCER RES, V54, P4845
[29]   Induction of the plasminogen activator inhibitor-1 gene expression by mild hypoxia via a hypoxia response element binding the hypoxia-inducible factor-1 in rat hepatocytes [J].
Kietzmann, T ;
Roth, U ;
Jungermann, K .
BLOOD, 1999, 94 (12) :4177-4185
[30]   THE NEW WHO CLASSIFICATION OF BRAIN-TUMORS [J].
KLEIHUES, P ;
BURGER, PC ;
SCHEITHAUER, BW .
BRAIN PATHOLOGY, 1993, 3 (03) :255-268