TAM family kinases as therapeutic targets at the interface of cancer and immunity

IF 81.1 1区 医学 Q1 ONCOLOGY
Deborah DeRyckere, Justus M. Huelse, H. Shelton Earp, Douglas K. Graham
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引用次数: 0

Abstract

Novel treatment approaches are needed to overcome innate and acquired mechanisms of resistance to current anticancer therapies in cancer cells and the tumour immune microenvironment. The TAM (TYRO3, AXL and MERTK) family receptor tyrosine kinases (RTKs) are potential therapeutic targets in a wide range of cancers. In cancer cells, TAM RTKs activate signalling pathways that promote cell survival, metastasis and resistance to a variety of chemotherapeutic agents and targeted therapies. TAM RTKs also function in innate immune cells, contributing to various mechanisms that suppress antitumour immunity and promote resistance to immune-checkpoint inhibitors. Therefore, TAM antagonists provide an unprecedented opportunity for both direct and immune-mediated therapeutic activity provided by inhibition of a single target, and are likely to be particularly effective when used in combination with other cancer therapies. To exploit this potential, a variety of agents have been designed to selectively target TAM RTKs, many of which have now entered clinical testing. This Review provides an essential guide to the TAM RTKs for clinicians, including an overview of the rationale for therapeutic targeting of TAM RTKs in cancer cells and the tumour immune microenvironment, a description of the current preclinical and clinical experience with TAM inhibitors, and a perspective on strategies for continued development of TAM-targeted agents for oncology applications. The TAM (TYRO3, AXL and MERTK) family receptor tyrosine kinases (RTKs) have diverse cancer-promoting functions in malignant cells as well as immune cells and other cell types in the tumour microenvironment, presenting an attractive opportunity for both direct and immune-mediated therapeutic activity manifest through inhibition of a single target. Accordingly, a variety of agents designed to selectively target TAM RTKs are entering clinical testing. This Review provides an essential guide to the TAM RTKs for clinicians. The authors comprehensively review the various roles of TAM RTKs in cancer, the evidence supporting their potential as therapeutic targets, and the translational development of TAM-targeted agents as cancer treatments.

Abstract Image

Abstract Image

TAM家族激酶作为癌症和免疫界面的治疗靶点。
需要新的治疗方法来克服癌症细胞和肿瘤免疫微环境中对当前抗癌疗法的固有和后天耐药性机制。TAM(TYRO3、AXL和MERTK)家族受体酪氨酸激酶(RTKs)是多种癌症的潜在治疗靶点。在癌症细胞中,TAM RTK激活信号通路,促进细胞存活、转移和对多种化疗药物和靶向治疗的抵抗。TAM RTKs也在先天免疫细胞中发挥作用,参与抑制抗肿瘤免疫和促进对免疫检查点抑制剂的抵抗的各种机制。因此,TAM拮抗剂为通过抑制单个靶点提供的直接和免疫介导的治疗活性提供了前所未有的机会,并且当与其他癌症疗法联合使用时可能特别有效。为了开发这一潜力,已经设计了多种药物来选择性靶向TAM RTK,其中许多现已进入临床测试。这篇综述为临床医生提供了TAM RTK的重要指南,包括对TAM RTKs在癌症细胞和肿瘤免疫微环境中的治疗靶向的基本原理的概述,对TAM抑制剂的当前临床前和临床经验的描述,以及对TAM靶向剂在肿瘤应用中的持续开发策略的展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
99.40
自引率
0.40%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Nature Reviews publishes clinical content authored by internationally renowned clinical academics and researchers, catering to readers in the medical sciences at postgraduate levels and beyond. Although targeted at practicing doctors, researchers, and academics within specific specialties, the aim is to ensure accessibility for readers across various medical disciplines. The journal features in-depth Reviews offering authoritative and current information, contextualizing topics within the history and development of a field. Perspectives, News & Views articles, and the Research Highlights section provide topical discussions, opinions, and filtered primary research from diverse medical journals.
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