Lee Kai-Ling, Lai Tsung-Ching, Lee Wei-Jiunn, Chen Yu-Chieh, Ho Kuo-Hao, Hung Wen-Yueh, Yang Yi-Chieh, Chan Ming-Hsien, Hsieh Feng-Koo, Chung Chi-Li, Chang Jer-Hwa, Chien Ming-Hsien
Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
Division of Pulmonary Medicine, Department of Internal Medicine, Taipei Medical University Hospital, Taipei 110301, Taiwan.
Cancers (Basel). 2023 Jun 22;15(13):3288. doi: 10.3390/cancers15133288.
Non-small-cell lung cancer (NSCLC) is a typical inflammation-associated cancer, and lung adenocarcinoma (LUAD) is the most common pathological subtype. Epidermal growth factor (EGF) receptor (EGFR) mutations are the most common driver mutations of LUAD, and they have been identified as important therapeutic targets by EGFR-tyrosine kinase inhibitors (TKIs). The proinflammatory cytokine, interleukin (IL)-17A, and IL-17A-producing cells were reported to be elevated in the tumor microenvironment and peripheral blood of NSCLC patients and to be correlated with tumor progression and poor prognoses. However, the pathophysiological role of IL-17A in NSCLC remains unclear, although some studies suggested its involvement in cancer cell invasion and metastasis. Herein, we observed that expressions of IL-17A and its receptor, IL-17 receptor C (IL-17RC), were elevated in LUAD tissues and were correlated with poor survival in different lung cancer cohorts. In LUAD cells with mutant EGFR, the IL-17A/IL-17RC axis was shown to enhance phosphorylation of EGFR and Met, thereby promoting proliferation and resistance to EGFR-TKIs such as afatinib. In LUAD cells with wild-type (WT) EGFR, we found that the IL-17A/IL-17RC axis enhanced EGF-induced EGFR activation and cell proliferation through causing impairment of EGF-induced EGFR lysosomal degradation. Collectively, our results indicated diverse impacts of the IL-17A/IL-17RC axis on EGFR activation in LUAD cells with WT and mutant EGFR and suggested that developing therapeutic strategies against IL-17A/IL-17RC would be valuable for LUAD treatment.
非小细胞肺癌(NSCLC)是一种典型的炎症相关癌症,肺腺癌(LUAD)是最常见的病理亚型。表皮生长因子(EGF)受体(EGFR)突变是LUAD最常见的驱动突变,并且它们已被表皮生长因子受体酪氨酸激酶抑制剂(TKIs)确定为重要的治疗靶点。据报道,促炎细胞因子白细胞介素(IL)-17A以及产生IL-17A的细胞在NSCLC患者的肿瘤微环境和外周血中升高,并且与肿瘤进展和不良预后相关。然而,IL-17A在NSCLC中的病理生理作用仍不清楚,尽管一些研究表明它参与癌细胞的侵袭和转移。在此,我们观察到IL-17A及其受体IL-17受体C(IL-17RC)在LUAD组织中的表达升高,并且与不同肺癌队列中的不良生存相关。在具有突变型EGFR的LUAD细胞中,IL-17A/IL-17RC轴显示可增强EGFR和Met的磷酸化,从而促进增殖并增强对阿法替尼等EGFR-TKIs的抗性。在具有野生型(WT)EGFR的LUAD细胞中,我们发现IL-17A/IL-17RC轴通过导致EGF诱导的EGFR溶酶体降解受损来增强EGF诱导的EGFR激活和细胞增殖。总体而言,我们的结果表明IL-17A/IL-17RC轴对具有WT和突变型EGFR的LUAD细胞中EGFR激活具有不同影响,并表明开发针对IL-17A/IL-17RC的治疗策略对LUAD治疗具有重要价值。