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靶向胰岛素样生长因子-1受体:龟兔赛跑的故事。

Targeting the IGF-1R: The Tale of the Tortoise and the Hare.

作者信息

Crudden Caitrin, Girnita Ada, Girnita Leonard

机构信息

Department of Oncology and Pathology, Cancer Centre Karolinska, Karolinska Institutet, Karolinska University Hospital , Stockholm , Sweden.

Department of Oncology and Pathology, Cancer Centre Karolinska, Karolinska Institutet, Karolinska University Hospital , Stockholm , Sweden ; Department of Dermatology, Karolinska University Hospital , Stockholm , Sweden.

出版信息

Front Endocrinol (Lausanne). 2015 Apr 27;6:64. doi: 10.3389/fendo.2015.00064. eCollection 2015.

Abstract

The insulin-like growth factor type 1 receptor (IGF-1R) plays a key role in the development and maintenance of cancer. Since the first links between growth factor receptors and oncogenes were noted over three decades ago, targeting the IGF-1R has been of great interest. This review follows the progress from inception through intense pharmaceutical development, disappointing clinical trials and recent updates to the signaling paradigm. In light of major developments in signaling understanding and activation complexities, we examine reasons for failure of first line targeting approaches. Recent findings include the fact that the IGF-1R can signal in the absence of the ligand, in the absence of kinase activity, and utilizes components of the GPCR system. With recognition of the unappreciated complexities that this first wave of targeting approaches encountered, we advocate re-recognition of IGF-1R as a valid target for cancer treatment and look to future directions, where both research and pharmaceutical strengths can lend themselves to finally unearthing anti-IGF-1R potential.

摘要

胰岛素样生长因子1型受体(IGF-1R)在癌症的发生和维持过程中起着关键作用。自三十多年前首次发现生长因子受体与癌基因之间的联系以来,靶向IGF-1R一直备受关注。本综述追踪了从最初构想到深入的药物研发、令人失望的临床试验以及信号转导模式的最新进展。鉴于在信号转导理解和激活复杂性方面的重大进展,我们探讨了一线靶向治疗方法失败的原因。最近的研究发现包括,IGF-1R可以在没有配体、没有激酶活性的情况下发出信号,并且利用GPCR系统的成分。认识到这一波靶向治疗方法所遇到的未被重视的复杂性后,我们主张重新将IGF-1R视为癌症治疗的有效靶点,并展望未来方向,届时研究和制药的优势都可助力最终挖掘抗IGF-1R的潜力。

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