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小鼠胶质瘤模型在临床前试验中的应用。

Applications of mouse glioma models in preclinical trials.

作者信息

Hu Xiaoyi, Holland Eric C

机构信息

Department of Cell Biology and Genetics, New York, NY 10021, USA.

出版信息

Mutat Res. 2005 Aug 25;576(1-2):54-65. doi: 10.1016/j.mrfmmm.2004.08.023.

Abstract

Gliomas are the most common primary tumors that arise from glial cells and their precursors in the central nervous system. Most of the genetic alterations identified in human gliomas result in signal transduction abnormalities or disruption of cell cycle arrest pathways. Over the past years, several mouse glioma models have been generated based on human genetic abnormalities and the induced gliomas exhibit histological similarities to their human counterparts. There is emerging evidence suggesting that an oncogenic signaling initiating tumorigenesis is also required for tumor maintenance, these glioma models can be used to further characterize the mechanisms of oncogenic signaling in tumor formation, as well as identify molecular targets in preclinical trials.

摘要

胶质瘤是中枢神经系统中最常见的起源于神经胶质细胞及其前体的原发性肿瘤。在人类胶质瘤中鉴定出的大多数基因改变都会导致信号转导异常或细胞周期停滞途径的破坏。在过去几年中,已经基于人类基因异常建立了几种小鼠胶质瘤模型,诱导产生的胶质瘤在组织学上与其人类对应物相似。越来越多的证据表明,启动肿瘤发生的致癌信号对于肿瘤维持也是必需的,这些胶质瘤模型可用于进一步表征肿瘤形成中致癌信号的机制,以及在临床前试验中鉴定分子靶点。

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