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胰岛素样生长因子受体 I 作为癌症治疗的靶点。

Insulin-like growth factor receptor type I as a target for cancer therapy.

机构信息

Centre d'Immunologie Pierre Fabre, 5 avenue Napoléon III, F-74164 Saint Julien-en-Genevois, France.

出版信息

Immunotherapy. 2009 Mar;1(2):265-79. doi: 10.2217/1750743X.1.2.265.

Abstract

In recent years, improvements in the understanding of oncogenesis has permitted the identification of new molecular targets for cancer therapy. Among all the different approaches, inhibition of tyrosine kinase receptor activity using small molecules or biomolecules for controlling cancer growth has been successful and has brought new therapeutic opportunities to the medical community. After more than 20 years of extensive work, insulin-like growth factor receptor I (IGF-IR) is becoming an attractive target for drug development. Owing to its close homology to insulin receptor, IGF-IR is of interest for antibody design while its specificity allows us to discriminate between the two receptors. Major efforts from a large number of pharmaceutical companies are invested in evaluating the efficacy of such molecules in humans. Discovery of biomarkers associated with efficacy and patient selection are the main challenges that we will have to deal with in order to target the appropriate patient population that will most benefit from anti-IGF-IR monoclonal antibodies and combined treatments. This review will provide an overview of the current knowledge on IGF-IR and ongoing clinical trials.

摘要

近年来,对致癌作用的认识的提高使得能够鉴定用于癌症治疗的新的分子靶标。在所有不同的方法中,使用小分子或生物分子抑制酪氨酸激酶受体活性以控制癌症生长已取得成功,并为医学界带来了新的治疗机会。经过 20 多年的广泛研究,胰岛素样生长因子受体 I(IGF-IR)正在成为药物开发的有吸引力的靶标。由于其与胰岛素受体的密切同源性,IGF-IR 对抗体设计很有意义,而其特异性允许我们区分这两个受体。许多制药公司投入了大量精力来评估此类分子在人体中的疗效。发现与疗效相关的生物标志物和患者选择是我们必须应对的主要挑战,以便针对最受益于抗 IGF-IR 单克隆抗体和联合治疗的合适患者人群。这篇综述将概述 IGF-IR 的现有知识和正在进行的临床试验。

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