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Fas(APO-1/CD95)信号通路在耐辐射的人胶质瘤细胞中是完整的。

Fas (APO-1/CD95) signaling pathway is intact in radioresistant human glioma cells.

作者信息

Yount G L, Levine K S, Kuriyama H, Haas-Kogan D A, Israel M A

机构信息

Preuss Laboratory for Molecular Neuro-oncology, Brain Tumor Research Center, Department of Neurological Surgery, University of California San Francisco, 94143, USA.

出版信息

Cancer Res. 1999 Mar 15;59(6):1362-5.

Abstract

Radiation-induced apoptosis can be mediated through pathways initiated by either DNA damage or ceramide-induced Fas signaling. Glioblastoma multiforme is a primary brain tumor that is highly resistant to irradiation, and U-87 MG, SF126, and T98G are glioblastoma-derived cell lines that mimic this characteristic. We found that these radioresistant glioma cells are susceptible to Fas-mediated cell death induced by treatment with either anti-Fas antibody or exogenous ceramide. Fas-mediated cell death in these cell lines is p53-independent. These data demonstrate that apoptosis can be induced by ceramide and mediated through the Fas pathway in glioma cells, although high-dose ionizing radiation fails to trigger this pathway.

摘要

辐射诱导的细胞凋亡可通过由DNA损伤或神经酰胺诱导的Fas信号传导启动的途径介导。多形性胶质母细胞瘤是一种对辐射高度耐药的原发性脑肿瘤,U-87 MG、SF126和T98G是模拟这种特征的胶质母细胞瘤衍生细胞系。我们发现,这些抗辐射的胶质瘤细胞易受抗Fas抗体或外源性神经酰胺处理诱导的Fas介导的细胞死亡影响。这些细胞系中Fas介导的细胞死亡不依赖p53。这些数据表明,神经酰胺可诱导胶质瘤细胞凋亡并通过Fas途径介导,尽管高剂量电离辐射未能触发该途径。

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