Li Xuan-Guang, Zhu Guang-Sheng, Cao Pei-Jun, Huang Hua, Chen Yu-Hao, Chen Chen, Chen Pei-Jie, Wu Di, Ding Chen, Zhang Zi-He, Zhang Rui-Hao, Hu Zi-Xuan, Zhao Wen-Hao, Liu Ming-Hui, Li Yong-Wen, Liu Hong-Yu, Chen Jun
Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Acta Pharmacol Sin. 2025 May;46(5):1419-1432. doi: 10.1038/s41401-024-01451-0. Epub 2025 Jan 14.
The emergence of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) has improved the prognosis for lung cancer patients with EGFR-driven mutations. However, acquired resistance to EGFR-TKIs poses a significant challenge to the treatment. Overcoming the resistance has primarily focused on developing next-generation targeted therapies based on the molecular mechanisms of resistance or inhibiting the activation of bypass pathways to suppress or reverse the resistance. In this study we developed a novel approach by using CRISPR-Cas9 whole-genome library screening to identify the genes that enhance the sensitivity of lung adenocarcinoma cells to EGFR-TKIs. Through this screening, we revealed integrin subunit alpha 8 (ITGA8) as the key gene that enhanced sensitivity to abivertinib in lung adenocarcinoma. Notably, ITGA8 expression was significantly downregulated in lung adenocarcinoma tissues compared to adjacent normal tissues. Bioinformatics analyses revealed that ITGA8 was positively correlated with the sensitivity of lung adenocarcinoma to abivertinib. We showed that knockdown of ITGA8 significantly enhanced the proliferation, migration and invasion of H1975 cells. Conversely, overexpression of ITGA8 reduced the proliferation migration and invasion of H1975/ABIR cells. Furthermore, we demonstrated that ITGA8 sensitized lung adenocarcinoma cells to EGFR-TKIs by attenuating the downstream FAK/SRC/AKT/MAPK signaling pathway. In H1975 cell xenograft mouse models, knockdown of ITGA8 significantly increased tumor growth and reduced the sensitivity to abivertinib, whereas overexpression of ITGA8 markedly suppressed tumor proliferation and enhanced sensitivity to the drug. This study demonstrates that ITGA8 inhibits the proliferation, invasion and migration of lung adenocarcinoma cells, enhances the sensitivity to EGFR-TKIs, improves treatment efficacy, and delays the progression of acquired resistance. Thus, ITGA8 presents a potential therapeutic candidate for addressing acquired resistance to EGFR-TKIs from a novel perspective.
表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)的出现改善了具有EGFR驱动突变的肺癌患者的预后。然而,对EGFR-TKIs的获得性耐药给治疗带来了重大挑战。克服耐药性主要集中在基于耐药分子机制开发下一代靶向疗法或抑制旁路途径的激活以抑制或逆转耐药性。在本研究中,我们开发了一种新方法,通过使用CRISPR-Cas9全基因组文库筛选来鉴定增强肺腺癌细胞对EGFR-TKIs敏感性的基因。通过该筛选,我们揭示整合素亚基α8(ITGA8)是增强肺腺癌对阿维替尼敏感性的关键基因。值得注意的是,与相邻正常组织相比,ITGA8在肺腺癌组织中的表达显著下调。生物信息学分析显示,ITGA8与肺腺癌对阿维替尼的敏感性呈正相关。我们发现敲低ITGA8显著增强了H1975细胞的增殖、迁移和侵袭能力。相反,ITGA8的过表达减少了H1975/ABIR细胞的增殖、迁移和侵袭。此外,我们证明ITGA8通过减弱下游FAK/SRC/AKT/MAPK信号通路使肺腺癌细胞对EGFR-TKIs敏感。在H1975细胞异种移植小鼠模型中,敲低ITGA8显著增加肿瘤生长并降低对阿维替尼的敏感性,而ITGA8的过表达显著抑制肿瘤增殖并增强对药物的敏感性。本研究表明,ITGA8抑制肺腺癌细胞的增殖、侵袭和迁移,增强对EGFR-TKIs的敏感性,提高治疗效果,并延缓获得性耐药的进展。因此,ITGA8从新的角度为解决对EGFR-TKIs的获得性耐药提供了一个潜在的治疗候选靶点。