Cracking the EGFR code: Cancer biology, resistance mechanisms, and future therapeutic frontiers.

IF 17.3 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Yafei Du, Feride Karatekin, Wendy Kehan Wang, Wanjin Hong, Gandhi T K Boopathy
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引用次数: 0

Abstract

Epidermal growth factor receptor (EGFR) plays a crucial role in tumorigenesis across multiple cancer types. EGFR mutations, overexpression, amplifications, dysregulated signaling, and impaired receptor downregulation drive cancer progression, particularly in non-small cell lung cancer, glioblastoma, colorectal cancer, gastric cancer, and head and neck cancers. Over the past decades, EGFR-targeted therapies, including tyrosine kinase inhibitors and monoclonal antibodies, have significantly improved patient outcomes. However, drug resistance inevitably arises through on-target mutations, activation of bypass signaling pathways, and disruptions in receptor trafficking and degradation. To overcome resistance, novel therapeutic strategies such as new generation of tyrosine kinase inhibitors, antibody-drug conjugates, and targeted protein degradation approaches like proteolysis-targeting chimeras are being actively explored. Additionally, combination therapies targeting parallel or compensatory pathways are being explored in mitigating drug resistance. Advances in genomic profiling and liquid biopsy technologies further enable personalized treatment strategies tailored to individual genetic backgrounds. In this review, we provide an overview of EGFR signaling and examine the landscape of EGFR mutations and currently available targeted therapies, while highlighting key resistance mechanisms. Furthermore, emerging strategies designed to overcome resistance are discussed, offering insights into future directions for EGFR-targeted cancer treatment. SIGNIFICANCE STATEMENT: Epidermal growth factor receptor (EGFR) is a key driver of tumorigenesis across multiple cancers, with overexpression, mutations, and amplifications promoting disease progression and therapeutic resistance. Despite the success of EGFR-targeted therapies, resistance remains a significant barrier to sustainable efficacy. This review provides an overview of EGFR biology and therapy, resistance mechanisms, and emerging new therapeutic strategies. A deeper understanding of these aspects is crucial for overcoming resistance and guiding the development of more effective and personalized cancer treatments.

破解EGFR密码:癌症生物学、耐药机制和未来治疗前沿。
表皮生长因子受体(EGFR)在多种癌症类型的肿瘤发生中起着至关重要的作用。EGFR突变、过表达、扩增、信号失调和受体下调受损驱动癌症进展,特别是在非小细胞肺癌、胶质母细胞瘤、结直肠癌、胃癌和头颈癌中。在过去的几十年里,egfr靶向治疗,包括酪氨酸激酶抑制剂和单克隆抗体,显著改善了患者的预后。然而,由于靶突变、旁路信号通路的激活以及受体运输和降解的中断,不可避免地会产生耐药性。为了克服耐药性,新的治疗策略,如新一代酪氨酸激酶抑制剂、抗体-药物偶联物和靶向蛋白质降解方法,如靶向蛋白质水解嵌合体,正在积极探索。此外,针对平行或代偿途径的联合治疗正在探索减轻耐药。基因组谱分析和液体活检技术的进步进一步使针对个体遗传背景的个性化治疗策略成为可能。在这篇综述中,我们提供了EGFR信号的概述,研究了EGFR突变的前景和目前可用的靶向治疗,同时强调了关键的耐药机制。此外,还讨论了旨在克服耐药性的新兴策略,为egfr靶向癌症治疗的未来方向提供了见解。意义声明:表皮生长因子受体(EGFR)是多种癌症肿瘤发生的关键驱动因素,其过表达、突变和扩增促进疾病进展和治疗耐药性。尽管egfr靶向治疗取得了成功,但耐药性仍然是持续疗效的重大障碍。本文综述了EGFR生物学和治疗、耐药机制以及新兴的治疗策略。深入了解这些方面对于克服耐药性和指导开发更有效和个性化的癌症治疗至关重要。
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来源期刊
Pharmacological Reviews
Pharmacological Reviews 医学-药学
CiteScore
34.70
自引率
0.50%
发文量
40
期刊介绍: Pharmacological Reviews is a highly popular and well-received journal that has a long and rich history of success. It was first published in 1949 and is currently published bimonthly online by the American Society for Pharmacology and Experimental Therapeutics. The journal is indexed or abstracted by various databases, including Biological Abstracts, BIOSIS Previews Database, Biosciences Information Service, Current Contents/Life Sciences, EMBASE/Excerpta Medica, Index Medicus, Index to Scientific Reviews, Medical Documentation Service, Reference Update, Research Alerts, Science Citation Index, and SciSearch. Pharmacological Reviews offers comprehensive reviews of new pharmacological fields and is able to stay up-to-date with published content. Overall, it is highly regarded by scholars.
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