Department of Urology, The Third Affiliated Hospital of Shenzhen University (Luohu Hospital Group), Shenzhen, China.
Shantou University Medical College, Shantou, China.
Medicine (Baltimore). 2023 Oct 6;102(40):e35086. doi: 10.1097/MD.0000000000035086.
During the course of treating non-small cell lung cancer (NSCLC) with epithelial growth factor receptor (EGFR) mutant, gefitinib resistance (GR) is unavoidable. As the environment for tumor cells to grow and survive, tumor microenvironment (TME) can significantly affect therapeutic response and clinical outcomes, offering new opportunities for addressing GR. Dynamic changes within the TME were identified during the treatment of gefitinib, suggesting the close relationship between TME and GR. Various dynamic processes like angiogenesis, hypoxia-pathway activation, and immune evasion can be blocked so as to synergistically enhance the therapeutic effects of gefitinib or reverse GR. Besides, cellular components like macrophages can be reprogrammed for the same purpose. In this review, we summarized recently proposed therapeutic targets to provide an overview of the potential roles of TME in treating gefitinib-resistant NSCLC, and discussed the difficulty of applying these targets in cancer treatment.
在使用表皮生长因子受体(EGFR)突变体治疗非小细胞肺癌(NSCLC)的过程中,吉非替尼耐药(GR)是不可避免的。肿瘤微环境(TME)是肿瘤细胞生长和存活的环境,它可以显著影响治疗反应和临床结果,为解决 GR 提供了新的机会。在吉非替尼治疗过程中发现 TME 内的动态变化,提示 TME 与 GR 之间存在密切关系。可以阻断各种动态过程,如血管生成、缺氧途径激活和免疫逃逸,以协同增强吉非替尼的治疗效果或逆转 GR。此外,还可以对巨噬细胞等细胞成分进行重编程以达到同样的目的。在这篇综述中,我们总结了最近提出的治疗靶点,以概述 TME 在治疗吉非替尼耐药 NSCLC 中的潜在作用,并讨论了将这些靶点应用于癌症治疗的困难。