Department of General Surgery, The First Hospital affiliated to Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Cancer Research Center, Xiamen University School of Medicine, Xiamen, China.
Ann Med. 2023 Dec;55(1):1298-1316. doi: 10.1080/07853890.2023.2192049.
This study aims to evaluate the prognostic value of m6A-associated long noncoding RNAs (lncRNAs) and their interaction with tumour microenvironment in thyroid cancer (THCA).
The clinical and gene expression data of tumours from 502 patients with THCA and 58 adjacent normal tissues were retrieved from The Cancer Genome Atlas (TCGA)-THCA dataset. The Pearson test was utilized to identify potential m6A-associated lncRNAs ( < 0.001 and Pearson correlation coefficient > 0.4). Quantitative real-time polymerase chain reaction was performed to verify the expression levels of lncRNAs in tissues. MTT, EdU, colony formation and wound-healing assays were performed to determine the functions of m6A-associated lncRNAs in THCA cell proliferation and metastasis.
M6A-associated lncRNAs were identified in three cluster groups. A significant survival difference was found among them, with cluster 1 patients showing worse survival. Moreover, lower immune and estimate scores were correlated to poorer prognosis, and CD8+ T cell and memory CD4+ T cell levels were increased in cluster 1. Cluster 2, with better overall survival, had high expression of PD-L1 and CTLA-4. Eleven of the m6A-associated lncRNAs were screened to establish the risk model, including AC007365.1, AC008555.1, AC040160.1, AC064807.1, AC126773.4, AL023583.1, AL512306.2, EIF2AK3-DT, LINC00667, LYPLAL1-DT and MIR181A2HG. Based on the median risk score, THCA patients were stratified into low-risk and high-risk groups. Overall survival analysis showed a dramatic difference between the two groups. qRCR was performed to verify the expression levels of lncRNA (LYPLAL1-DT, EIF2AK3-DT and MIR181A2HG) in THCA and adjacent normal tissues. Furthermore, functional experiments showed that knockdown of MIR181A2HG obviously inhibited the proliferation and migration of papillary thyroid cancer (PTC) cells , whereas LYPLAL1-DT overexpression promoted PTC cell proliferation and migration.
Eleven of the m6A-associated lncRNAs were identified as a risk model to predict clinical outcomes and provide a novel and efficient immunotherapeutic strategy for THCA patients.Key messagesm6A-associated lncRNAs can be used to predict the clinical outcomes of thyroid cancer patients.An m6A-associated lncRNAs risk model, which can accurately evaluate the immune status and risk stratification in individual thyroid cancer patients, was established.Knockdown/overexpression of representative lncRNAs in the risk model significantly affected the proliferation and migration of papillary thyroid cancer cells.
本研究旨在评估 m6A 相关长链非编码 RNA(lncRNA)及其与甲状腺癌(THCA)肿瘤微环境相互作用的预后价值。
从癌症基因组图谱(TCGA)-THCA 数据库中检索了 502 例 THCA 患者和 58 例相邻正常组织的临床和基因表达数据。采用 Pearson 检验鉴定潜在的 m6A 相关 lncRNA(<0.001,Pearson 相关系数>0.4)。通过 qRT-PCR 验证 lncRNA 在组织中的表达水平。MTT、EdU、集落形成和划痕愈合实验用于确定 m6A 相关 lncRNA 在 THCA 细胞增殖和转移中的功能。
在三个聚类组中鉴定出 m6A 相关 lncRNA。它们之间存在显著的生存差异,其中聚类 1 患者的生存情况较差。此外,免疫和估计评分较低与预后不良相关,并且聚类 1 中 CD8+T 细胞和记忆 CD4+T 细胞水平升高。具有更好总生存率的聚类 2 具有高 PD-L1 和 CTLA-4 表达。筛选出 11 个 m6A 相关 lncRNA 构建风险模型,包括 AC007365.1、AC008555.1、AC040160.1、AC064807.1、AC126773.4、AL023583.1、AL512306.2、EIF2AK3-DT、LINC00667、LYPLAL1-DT 和 MIR181A2HG。基于中位数风险评分,将 THCA 患者分为低风险和高风险组。总生存分析显示两组之间存在显著差异。通过 qRCR 验证了 lncRNA(LYPLAL1-DT、EIF2AK3-DT 和 MIR181A2HG)在 THCA 和相邻正常组织中的表达水平。此外,功能实验表明,MIR181A2HG 的敲低明显抑制了甲状腺乳头状癌(PTC)细胞的增殖和迁移,而 LYPLAL1-DT 的过表达则促进了 PTC 细胞的增殖和迁移。
鉴定出 11 个 m6A 相关 lncRNA 可作为预测甲状腺癌患者临床结局的风险模型,并为 THCA 患者提供了一种新的有效的免疫治疗策略。
m6A 相关 lncRNA 可用于预测甲状腺癌患者的临床结局。建立了一个 m6A 相关 lncRNAs 风险模型,可准确评估个体甲状腺癌患者的免疫状态和风险分层。代表风险模型中 lncRNA 的敲低/过表达显著影响甲状腺乳头状癌细胞的增殖和迁移。