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在小鼠模型中,白细胞介素-6是胶质瘤发展所必需的。

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

作者信息

Weissenberger Jakob, Loeffler Sébastien, Kappeler Andreas, Kopf Manfred, Lukes Anton, Afanasieva Tatiana A, Aguzzi Adriano, Weis Joachim

机构信息

Division of Neuropathology, Institute of Pathology, University of Bern, Murtenstrasse 31, Bern CH-3010, Switzerland.

出版信息

Oncogene. 2004 Apr 22;23(19):3308-16. doi: 10.1038/sj.onc.1207455.

Abstract

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.

摘要

多效细胞因子白细胞介素-6(IL-6)促进多种癌症类型的恶性进展和抗凋亡。尽管恶性胶质瘤中IL-6水平升高,且胶质瘤细胞对IL-6有反应,但其在胶质瘤发生中的功能作用尚不清楚。我们通过将胶质纤维酸性蛋白(GFAP)-病毒src癌基因转基因小鼠与IL-6缺陷小鼠杂交,在自发性星形细胞瘤小鼠模型中研究了IL-6的这一作用。我们在此表明,IL-6的缺失可防止这些易感动物形成肿瘤,但不影响肿瘤前星形细胞增生。此外,我们在51例世界卫生组织II-IV级人类胶质瘤和所有研究的实验性小鼠肿瘤中证实了转录因子信号转导子和转录激活子(STAT)3的磷酸化和核转位,这是IL-6信号传导的一个前提条件。连同STAT3激活随恶性程度增加的观察结果,这些发现表明IL-6在星形细胞瘤的发生和恶性进展中起重要作用。

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