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癌症中的表皮生长因子受体(ErbB)及其信号通路

ErbB receptors and signaling pathways in cancer.

作者信息

Hynes Nancy E, MacDonald Gwen

机构信息

Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.

出版信息

Curr Opin Cell Biol. 2009 Apr;21(2):177-84. doi: 10.1016/j.ceb.2008.12.010. Epub 2009 Feb 7.

Abstract

The ErbB receptor tyrosine kinases play important roles in normal physiology and in cancer. Epidermal growth factor receptor (EGFR) and ErbB2 in particular are mutated in many epithelial tumors, and clinical studies suggest that they play roles in cancer development and progression. These receptors have been intensely studied, not only to understand the mechanisms underlying their oncogenic potential, but also to exploit them as therapeutic targets. ErbB receptors activate a multiplicity of intracellular pathways via their ability to interact with numerous signal transducers. Furthermore, there are now many ErbB-targeted inhibitors used in the clinic. In this review we will concentrate on breast tumors with ERBB2 gene amplification/receptor overexpression and non-small cell lung cancer (NSCLC) with activating EGFR mutations. We will discuss data showing the important role that the PI3K/Akt pathway plays, not only in cancer development, but also in response to targeted therapies. Finally, mechanisms contributing to resistance to ErbB-targeted therapeutics will also be discussed.

摘要

ErbB受体酪氨酸激酶在正常生理和癌症中发挥重要作用。特别是表皮生长因子受体(EGFR)和ErbB2在许多上皮肿瘤中发生突变,临床研究表明它们在癌症发展和进展中起作用。这些受体已得到深入研究,不仅是为了了解其致癌潜力背后的机制,也是为了将它们作为治疗靶点加以利用。ErbB受体通过与众多信号转导分子相互作用的能力激活多种细胞内途径。此外,目前临床上有许多针对ErbB的抑制剂。在本综述中,我们将专注于具有ERBB2基因扩增/受体过表达的乳腺肿瘤以及具有激活型EGFR突变的非小细胞肺癌(NSCLC)。我们将讨论数据表明PI3K/Akt途径不仅在癌症发展中,而且在对靶向治疗的反应中所起的重要作用。最后,还将讨论导致对ErbB靶向治疗产生耐药性的机制。

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