Center of Multidisciplinary Technology for Advanced Medicine (CMUTEAM), Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Clinical Epidemiology and Clinical Statistics Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Int J Mol Sci. 2023 Mar 2;24(5):4827. doi: 10.3390/ijms24054827.
The discovery of potent EGFR-tyrosine kinase inhibitors (EGFR-TKIs) has revolutionized the treatment of EGFR-mutated lung cancer. Despite the fact that EGFR-TKIs have yielded several significant benefits for lung cancer patients, the emergence of resistance to EGFR-TKIs has been a substantial impediment to improving treatment outcomes. Understanding the molecular mechanisms underlying resistance is crucial for the development of new treatments and biomarkers for disease progression. Together with the advancement in proteome and phosphoproteome analysis, a diverse set of key signaling pathways have been successfully identified that provide insight for the discovery of possible therapeutically targeted proteins. In this review, we highlight the proteome and phosphoproteomic analyses of non-small cell lung cancer (NSCLC) as well as the proteome analysis of biofluid specimens that associate with acquired resistance in response to different generations of EGFR-TKI. Furthermore, we present an overview of the targeted proteins and potential drugs that have been tested in clinical studies and discuss the challenges of implementing this discovery in future NSCLC treatment.
针对 EGFR 突变型肺癌,高效的 EGFR 酪氨酸激酶抑制剂(EGFR-TKIs)的发现带来了治疗方式的变革。尽管 EGFR-TKIs 为肺癌患者带来了诸多显著获益,但 EGFR-TKIs 耐药的出现仍是改善治疗效果的重大阻碍。了解耐药背后的分子机制对于开发新的治疗方法和疾病进展的生物标志物至关重要。随着蛋白质组学和磷酸化蛋白质组学分析的进步,人们成功鉴定出了一系列多样化的关键信号通路,为可能的治疗靶点蛋白的发现提供了思路。在本文中,我们重点介绍了非小细胞肺癌(NSCLC)的蛋白质组学和磷酸化蛋白质组学分析,以及针对不同代 EGFR-TKI 获得性耐药的生物体液标本的蛋白质组学分析。此外,我们概述了在临床试验中已进行测试的靶向蛋白和潜在药物,并讨论了在未来 NSCLC 治疗中实施这一发现所面临的挑战。