Department of Radiotherapy, The Second People's Hospital of Wuhu, Wuhu 241001, China.
Department of Oncology, Key Laboratory of Cancer Molecular and Translational Research, The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.
J Environ Pathol Toxicol Oncol. 2024;43(4):1-11. doi: 10.1615/JEnvironPatholToxicolOncol.2024052122.
Lung adenocarcinoma (LUAD) is a subtype of lung cancer that occurs frequently and results in high mortality and morbidity, comprising almost 50% of all cases with the disease. Previously, long non-coding RNAs (lncRNAs) was evidenced to be helpful in the diagnosis and prognosis of LUAD. lncRNA AGAP11 was identified as a dysregulated lncRNA in LUAD. Whether AGAP11 is linked to the progression and prognosis of LUAD has not been known. The purpose was to probe the action of AGAP11 in the LUAD progression together with its intrinsic mechanism, with a view to supplying a perspective biomarker and therapeutic target for LUAD. AGAP11 expression in LUAD was analyzed by searching in the GEPIA database and conducting RT-qPCR. The significance of AGAP11 for the prognosis of LUAD was assessed by statistical analyses. The targeting relationship between AGAP11 and miR-494-3p was corroborated with Dual-luciferase reporter assay. The role of AGAP11 on cellular processes in LUAD cells was evaluated by CCK-8 and Transwell assays. AGAP11 was markedly down-regulated in LUAD and tightly correlated with TNM stage, lymph node metastasis, and tumor differentiation degree of patients. Down-regulation of AGAP11 was found to predict a dismal prognosis of LUAD. AGAP11 negatively modulated miR-494-3p expression by interacting with it. The growth, migration, and invasion of LUAD cells could be impaired by AGAP11 overexpression, which would be attenuated by the enhanced miR-494-3p expression. AGAP11 acted as a predictor for prognosis and curbed LUAD progression through modulating miR-494-3p.
肺腺癌 (LUAD) 是一种常见的肺癌亚型,其死亡率和发病率较高,几乎占所有肺癌病例的 50%。此前,长链非编码 RNA (lncRNA) 已被证明有助于 LUAD 的诊断和预后。lncRNA AGAP11 被鉴定为 LUAD 中失调的 lncRNA。AGAP11 是否与 LUAD 的进展和预后有关尚不清楚。本研究旨在探讨 AGAP11 在 LUAD 进展中的作用及其内在机制,以期为 LUAD 提供有前景的生物标志物和治疗靶点。通过在 GEPIA 数据库中搜索和进行 RT-qPCR 分析 LUAD 中的 AGAP11 表达。通过统计学分析评估 AGAP11 对 LUAD 预后的意义。通过双荧光素酶报告实验证实 AGAP11 与 miR-494-3p 的靶向关系。通过 CCK-8 和 Transwell 测定评估 AGAP11 在 LUAD 细胞中对细胞过程的作用。AGAP11 在 LUAD 中明显下调,与患者的 TNM 分期、淋巴结转移和肿瘤分化程度密切相关。AGAP11 下调预示 LUAD 预后不良。AGAP11 通过与 miR-494-3p 相互作用负调控 miR-494-3p 的表达。AGAP11 过表达可损害 LUAD 细胞的生长、迁移和侵袭,而增强的 miR-494-3p 表达可减弱这种作用。AGAP11 可作为预后预测因子,通过调节 miR-494-3p 抑制 LUAD 进展。