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Eag1作为一种癌症靶点。

Eag1 as a cancer target.

作者信息

Pardo Luis A, Sühmer Walter

机构信息

Max Planck Institute of Experimental Medicine, Department of Molecular Biology of Neuronal Signals, Hermann-Rein-Str 3, 37075 Göttingen, Germany.

出版信息

Expert Opin Ther Targets. 2008 Jul;12(7):837-43. doi: 10.1517/14728222.12.7.837.

Abstract

BACKGROUND

Ion channels are drug targets for many diseases but have only recently started to be regarded as potential primary cancer targets. Many types of ion channels have been identified that could be useful in cancer management.

OBJECTIVE

We focus on a voltage-gated potassium channel, ether à go-go 1 (Eag)1, which shows distinctive features such as a restricted expression pattern and peculiar electrophysiological properties.

METHODS

We review the literature on this channel and try to relate this knowledge to the context of other ion channels in cancer.

RESULTS/CONCLUSION: Eag1 appears to be a promising cancer target, both as a tumor marker because of restricted expression, which could be useful in the context of therapeutic decisions, and as a therapeutic-agent-targeting molecule.

摘要

背景

离子通道是许多疾病的药物靶点,但直到最近才开始被视为潜在的原发性癌症靶点。已经鉴定出多种可能对癌症治疗有用的离子通道类型。

目的

我们关注一种电压门控钾通道,即去极化激活延迟整流钾通道1(Eag)1,它具有独特的特征,如表达模式受限和特殊的电生理特性。

方法

我们回顾了关于该通道的文献,并试图将这些知识与癌症中其他离子通道的情况联系起来。

结果/结论:Eag1似乎是一个有前景的癌症靶点,既因其表达受限可作为肿瘤标志物,有助于治疗决策,又可作为治疗药物的靶向分子。

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