Location-dependent role of the human glioma cell peripheral-type benzodiazepine receptor in proliferation and steroid biosynthesis

被引：54

作者：

Brown, RC

Degenhardt, B

Kotoula, M

Papadopoulous, V ^{[1
]}

机构：

[1] Georgetown Univ, Med Ctr, Interdisciplinary Program Neurosci, Washington, DC 20007 USA

[2] Georgetown Univ, Med Ctr, Dept Cell Biol, Div Hormone Res, Washington, DC 20007 USA

[3] Georgetown Univ, Med Ctr, Dept Pharmacol, Washington, DC 20007 USA

[4] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20007 USA

[5] Georgetown Univ, Med Ctr, Lombardi Canc Ctr, Washington, DC 20007 USA

来源：

CANCER LETTERS | 2000年 / 156卷 / 02期

关键词：

neurosteroids; steroidogenesis; glioma; human; tumor biopsy;

D O I：

10.1016/S0304-3835(00)00451-1

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

We examined the localization and function of the peripheral-type benzodiazepine receptor (PBR), a protein highly expressed in steroidogenic tissues and aggressive tumor cells, in cell lines derived from glioblastoma multiforme tumors. In MGM-1 cells, PER is located in the nucleus, and cells proliferate in response to PER ligands but do not synthesize steroids de novo. In MGM-3 cells, PER is located in mitochondria and the cells synthesize steroids, but do not proliferate in response to PER ligands. In glioblastoma biopsies, PER is expressed in the nuclei of cells, while it is found in the cytosol of astrocytomas, and is absent from meningioma and medulloblastoma tumor biopsies. These data suggest that the subcellular localization of PER defines its function. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.

引用

页码：125 / 132

页数：8

共 17 条

[1] In vivo regulation of peripheral-type benzodiazepine receptor and glucocorticoid synthesis by Ginkgo biloba extract EGb 761 and isolated ginkgolides [J].