IL-6 is required for glioma development in a mouse model

被引:0
|
作者
Jakob Weissenberger
Sébastien Loeffler
Andreas Kappeler
Manfred Kopf
Anton Lukes
Tatiana A Afanasieva
Adriano Aguzzi
Joachim Weis
机构
[1] Institute of Pathology,Division of Neuropathology
[2] University of Bern,Department of Environmental Sciences
[3] Murtenstrasse 31,Department of Neurosurgery
[4] Molecular Biomedicine,undefined
[5] Swiss Federal Institute of Technology,undefined
[6] Wagistr. 27,undefined
[7] Inselspital,undefined
[8] University of Bern,undefined
[9] Institute of Neuropathology,undefined
[10] University of Zurich,undefined
[11] Schmelzbergstrasse 12,undefined
[12] Institute of Neuropathology,undefined
[13] University Hospital,undefined
[14] RWTH,undefined
来源
Oncogene | 2004年 / 23卷
关键词
gliomas; mouse model; IL-6 knockout; STAT3 signalling;
D O I
暂无
中图分类号
学科分类号
摘要
The pleiotropic cytokine interleukin-6 (IL-6) contributes to malignant progression and apoptosis resistance of various cancer types. Although IL-6 is elevated in malignant gliomas, and glioma cells respond to IL-6, its functional role in gliomagenesis is unclear. We have investigated this role of IL-6 in a mouse model of spontaneous astrocytoma by crossbreeding glial fibrillary acidic protein (GFAP)-viral src oncogene transgenic mice with IL-6-deficient mice. We show here that ablation of IL-6 prevents tumour formation in these predisposed animals, but did not affect preneoplastic astrogliosis. Moreover, we demonstrate phosphorylation and nuclear translocation of the transcription factor signal transducer and activator of transcription (STAT)3, a prerequisite for IL-6 signalling, in 51 human gliomas WHO grade II–IV and all experimental mouse tumours investigated. Together with the observation that STAT3 activation increases with malignancy, these findings indicate an important role for IL-6 in the development and malignant progression of astrocytomas.
引用
收藏
页码:3308 / 3316
页数:8
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