Expression of granulocyte colony-stimulating factor in recurrent glial tumors is inversely correlated with tumor progression

被引:9
|
作者
Stan, AC
Walter, GF
Welte, K
Schneider, B
Bona, CA
Pietsch, T
机构
[1] CUNY Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
[2] Hannover Med Sch, Inst Neuropathol, D-30625 Hannover, Germany
[3] Hannover Med Sch, Dept Pediat Hematol & Oncol, D-30625 Hannover, Germany
[4] Hannover Med Sch, Dept Biometr, D-30625 Hannover, Germany
[5] Univ Bonn, Inst Neuropathol, D-53127 Bonn, Germany
关键词
G-CSF; glioma; differentiation; recurrence; densitometry;
D O I
10.1016/S0165-5728(98)00225-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have previously reported that in vivo-expression of granulocyte colony-stimulating factor (G-CSF) is a characteristic feature of reactive and neoplastic astrocytes. The aim of the present study was to analyze the expression of G-CSF protein in primary and recurrent astroglial, oligodendroglial and mixed glial-differentiated tumors. G-CSF expression was present in all GFAP-positive tumors excepting glioblastomas. G-CSF expression was significantly reduced in recurrent tumors more dedifferentiated than their primary counterparts. G-CSF expression was absent in all GFAP-negative tumors such as oligodendrogliomas. Our results demonstrate that G-CSF is a highly sensitive differentiation marker of neoplastic astrocytes, which is lost during tumor progression. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:66 / 73
页数:8
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