Cha Jeong Eun, Bae Woom-Yee, Choi Jae-Sun, Lee Seung Hyeun, Jeong Joo-Won
Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Department of Anatomy and Neurobiology, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Oncol Lett. 2021 Sep;22(3):671. doi: 10.3892/ol.2021.12932. Epub 2021 Jul 18.
Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) have been used to treat patients with non-small cell lung cancer (NSCLC) and activating EGFR mutations; however, the emergence of secondary mutations in EGFR or the acquisition of resistance to EGFR-TKIs can develop and is involved in clinical failure. Since angiogenesis is associated with tumor progression and the blockade of antitumor drugs, inhibition of angiogenesis could be a rational strategy for developing anticancer drugs combined with EGFR-TKIs to treat patients with NSCLC. The signaling pathway mediated by hypoxia-inducible factor-1 (HIF-1) is essential for tumor angiogenesis. The present study aimed to identify the dependence of gefitinib resistance on HIF-1α activity using angiogenesis assays, western blot analysis, colony formation assay, xenograft tumor mouse model and immunohistochemical analysis of tumor tissues. In the NSCLC cell lines, HIF-1α protein expression levels and hypoxia-induced angiogenic activities were found to be increased. In a xenograft mouse tumor model, tumor tissues derived from gefitinib-resistant PC9 cells showed increased protein expression of HIF-1α and angiogenesis within the tumors. Furthermore, inhibition of HIF-1α suppressed resistance to gefitinib, whereas overexpression of HIF-1α increased resistance to gefitinib. The results from the present study provides evidence that HIF-1α was associated with the acquisition of resistance to gefitinib and suggested that inhibiting HIF-1α alleviated gefitinib resistance in NSCLC cell lines.
表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKIs)已被用于治疗非小细胞肺癌(NSCLC)且具有激活型EGFR突变的患者;然而,EGFR继发性突变的出现或对EGFR-TKIs耐药性的获得会发生,并导致临床治疗失败。由于血管生成与肿瘤进展及抗肿瘤药物的阻断相关,抑制血管生成可能是开发与EGFR-TKIs联合使用的抗癌药物来治疗NSCLC患者的合理策略。由缺氧诱导因子-1(HIF-1)介导的信号通路对肿瘤血管生成至关重要。本研究旨在通过血管生成检测、蛋白质印迹分析、集落形成检测、异种移植肿瘤小鼠模型以及肿瘤组织的免疫组化分析,确定吉非替尼耐药对HIF-1α活性的依赖性。在NSCLC细胞系中,发现HIF-1α蛋白表达水平和缺氧诱导的血管生成活性增加。在异种移植小鼠肿瘤模型中,源自吉非替尼耐药PC9细胞的肿瘤组织显示肿瘤内HIF-1α蛋白表达增加和血管生成增加。此外,抑制HIF-1α可抑制对吉非替尼的耐药性,而HIF-1α的过表达则增加对吉非替尼的耐药性。本研究结果提供了证据表明HIF-1α与获得对吉非替尼的耐药性相关,并表明抑制HIF-1α可减轻NSCLC细胞系中的吉非替尼耐药性。