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我们应该对表皮生长因子受体(EGFR)抑制剂的反应不佳感到惊讶吗?

Should we be surprised at the paucity of response to EGFR inhibitors?

作者信息

Gusterson Barry A, Hunter Keith D

机构信息

Department of Pathology, Division of Cancer Sciences and Molecular Pathology, Faculty of Medicine, University of Glasgow, Western Infirmary, Glasgow, UK.

出版信息

Lancet Oncol. 2009 May;10(5):522-7. doi: 10.1016/S1470-2045(09)70034-8.

Abstract

Data suggest that neither our current understanding of the function and signalling of epidermal growth factor receptor (EGFR), nor measurements of receptor expression are reliably predictive of therapeutic responses to EGFR inhibitors. The time has now come to consider whether such poor correlation between receptor expression and clinical response is caused by poor assays or by more fundamental issues relating to the in-vivo function of EGFR. Revisiting some of the early findings of the biology of EGFR function and understanding the limitations of immunohistochemistry as a quantitative technique might provide some clues. However, we still have a lot to learn about this receptor, its many ligands, and its binding partners in normal physiology and disease.

摘要

数据表明,我们目前对表皮生长因子受体(EGFR)功能和信号传导的理解,以及受体表达的测量,都不能可靠地预测对EGFR抑制剂的治疗反应。现在是时候考虑受体表达与临床反应之间如此糟糕的相关性是由检测方法不佳还是与EGFR体内功能相关的更基本问题所导致的了。回顾一些关于EGFR功能生物学的早期发现,并了解免疫组织化学作为一种定量技术的局限性,可能会提供一些线索。然而,关于这个受体、它的许多配体以及它在正常生理和疾病中的结合伙伴,我们仍有很多需要了解的地方。

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