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肿瘤及肿瘤微环境中的Eph受体酪氨酸激酶

Eph receptor tyrosine kinases in tumor and tumor microenvironment.

作者信息

Brantley-Sieders Dana, Schmidt Sonja, Parker Monica, Chen Jin

机构信息

Vanderbilt Ingram Cancer Center, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

出版信息

Curr Pharm Des. 2004;10(27):3431-42. doi: 10.2174/1381612043383160.

Abstract

Eph receptors are a unique family of receptor tyrosine kinases (RTK) that play critical roles in embryonic patterning, neuronal targeting, and vascular development during embryogenesis. In adults, Eph RTKs and their ligands, the ephrins, are frequently overexpressed in a variety of cancers and tumor cell lines, including breast, prostate, non-small cell lung and colon cancers, melanomas, and neuroblastomas. Unlike traditional oncogenes that often function only in tumor cells, recent data show that Eph receptors mediate cell-cell interaction both in tumor cells and in tumor microenvironment, namely the tumor stroma and tumor vasculature. As such, Eph RTKs represent attractive potential targets for drug design, as targeting these molecules could attack several aspects of tumor progression simultaneously. This review will focus on recent advances in dissecting the role of Eph RTKs in tumor cells, tumor angiogenesis, and possible contribution to trafficking of inflammatory cells in cancer.

摘要

Eph受体是一类独特的受体酪氨酸激酶(RTK)家族,在胚胎发育过程中的胚胎模式形成、神经元靶向和血管发育中发挥关键作用。在成年人中,Eph RTK及其配体——ephrin,在多种癌症和肿瘤细胞系中经常过度表达,包括乳腺癌、前列腺癌、非小细胞肺癌和结肠癌、黑色素瘤以及神经母细胞瘤。与通常仅在肿瘤细胞中发挥作用的传统癌基因不同,最近的数据表明,Eph受体在肿瘤细胞以及肿瘤微环境(即肿瘤基质和肿瘤脉管系统)中均介导细胞间相互作用。因此,Eph RTK是药物设计中颇具吸引力的潜在靶点,因为靶向这些分子可以同时攻击肿瘤进展的多个方面。本综述将聚焦于剖析Eph RTK在肿瘤细胞、肿瘤血管生成中的作用以及对癌症中炎症细胞迁移可能的贡献方面的最新进展。

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