Han Linzhi, Shi Hongjie, Ma Shijing, Luo Yuan, Sun Wenjie, Li Shuying, Zhang Nannan, Jiang Xueping, Gao Yanping, Huang Zhengrong, Xie Conghua, Gong Yan
Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Department of Thoracic and Cardiovascular Surgery, Zhongnan Hospital of Wuhan University, Wuhan, China.
Front Oncol. 2022 Jan 17;11:804418. doi: 10.3389/fonc.2021.804418. eCollection 2021.
Non-small cell lung cancer (NSCLC) has high mortality rates worldwide. Agrin contributes to immune synapse information and is involved in tumor metastasis. However, its roles in NSCLC and tumor immune microenvironment remain unclear. This study examined the effects and the underlying mechanisms of Agrin in NSCLC and tumor-infiltrated immune cells. Clinical tissue samples were used to confirm the bioinformatic predictions. NSCLC cells were used to investigate the effects of Agrin on cell cycle and proliferation, as well as invasion and migration. Tumor xenograft mouse model was used to confirm the effects of Agrin on NSCLC growth and tumor-infiltrated regulatory T cells (Tregs) . Agrin levels in NSCLC cells were closely related to tumor progression and metastasis, and its function was enriched in the PI3K/AKT pathway. assays demonstrated that Agrin knockdown suppressed NSCLC cell proliferation and metastasis, while PI3K/AKT activators reversed the inhibitory effects of Agrin deficiency on NSCLC cell behaviors. Agrin expression was negatively associated with immunotherapy responses in NSCLC patients. Agrin knockdown suppressed Tregs, as well as interleukin (IL)-6 expression and secretion, while PI3K/AKT activators and exogenous IL-6 rescued the inhibitory effects. In the mouse model, Agrin downregulation alleviated NSCLC cell growth and Treg infiltration . Our results indicated that Agrin promotes tumor cell growth and Treg infiltration increasing IL-6 expression and secretion through PI3K/AKT pathway in NSCLC. Our studies suggested Agrin as a therapeutically potential target to increase the efficacy of immunotherapy in NSCLC patients.
非小细胞肺癌(NSCLC)在全球范围内具有较高的死亡率。聚集蛋白有助于免疫突触信息传递,并参与肿瘤转移。然而,其在NSCLC和肿瘤免疫微环境中的作用仍不清楚。本研究探讨了聚集蛋白在NSCLC和肿瘤浸润免疫细胞中的作用及潜在机制。使用临床组织样本证实生物信息学预测。利用NSCLC细胞研究聚集蛋白对细胞周期、增殖以及侵袭和迁移的影响。采用肿瘤异种移植小鼠模型证实聚集蛋白对NSCLC生长和肿瘤浸润调节性T细胞(Tregs)的影响。NSCLC细胞中的聚集蛋白水平与肿瘤进展和转移密切相关,其功能在PI3K/AKT通路中富集。实验表明,敲低聚集蛋白可抑制NSCLC细胞增殖和转移,而PI3K/AKT激活剂可逆转聚集蛋白缺乏对NSCLC细胞行为的抑制作用。聚集蛋白表达与NSCLC患者的免疫治疗反应呈负相关。敲低聚集蛋白可抑制Tregs以及白细胞介素(IL)-6的表达和分泌,而PI3K/AKT激活剂和外源性IL-6可挽救这种抑制作用。在小鼠模型中,下调聚集蛋白可减轻NSCLC细胞生长和Treg浸润。我们的结果表明,聚集蛋白通过PI3K/AKT通路增加IL-6的表达和分泌,从而促进肿瘤细胞生长和Treg浸润。我们的研究表明,聚集蛋白是提高NSCLC患者免疫治疗疗效的潜在治疗靶点。