河北医科大学学报 ›› 2023, Vol. 44 ›› Issue (2): 161-166.doi: 10.3969/j.issn.1007-3205.2023.02.008

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基于生物信息学分析LncRNA AC005479.2在甲状腺乳头状癌中的表达及相关分析

  

  1. 河北省邯郸市邯钢医院甲状腺科,河北 邯郸 056000

  • 出版日期:2023-02-25 发布日期:2023-02-28
  • 作者简介:梁新科(1981-),男,河北磁县人,河北省邯郸市邯钢医院主治医师,医学学士,从事甲状腺疾病诊治研究。
  • 基金资助:
    邯郸市科学技术研究与发展计划项目任务(19422083015-3)

Expression and correlation analysis of LncRNA AC005479.2 in papillary thyroid carcinoma based on bioinformatics

  1. Department of Thyroid, Handan Iron and Steel Hospital, Hebei Province, Handan 056000, China

  • Online:2023-02-25 Published:2023-02-28

摘要: 的关键基因及其潜在调控分子靶标,探索其在PTC中的分子调控机制。
方法 通过TCGA数据库检索并下载甲状腺乳头状癌的基因表达谱,使用Rstudio中的“Limma”软件包寻找甲状腺乳头状癌与癌旁组织之间的是否存在差异长链非编码RNA(long non-coding RNA, lncRNA)。使用WGCNA构建及临床相关性分析。通过GSEA进行富集分析和注释。
结果 经TCGA数据库筛选,共510例甲状腺乳头状癌的肿瘤组织与58例癌旁组织被纳入分析,共得到了58个差异表达lncRNA,其中包括36个高表达基因与22个低表达的基因。使用动态树切割法识别基因模块,设定模块内最低基因个数为100,最终得到11个相应的模块,结果显示,蓝色模块与甲状腺乳头状癌显著相关。蓝色模块内差异lncRNA共有34个,对Blue模块内34个差异lncRNA进行单因素和多因素Cox回归分析,得到AC005479.2。随后对AC005479.2绘制受试者工作特征曲线,曲线下面积为0.838。通过GO和KEGG分析,揭示AC005479.2的潜在通路与功能,结果显示AC005479.2可能通过脂肪细胞因子信号途径、MAPK信号通路、钙黏蛋白结合参与细胞黏附、对凋亡信号通路的正调控等功能参与甲状腺乳头状癌的病理过程。
结论 AC005479.2在甲状腺乳头状癌患者与健康人群的甲状腺组织的表达差异有统计学意义,AC005479.2基因有望成为甲状腺乳头状癌的生物标志基因,为后续的PTC的研究提供重要依据。


关键词: 甲状腺癌,乳头状, 生物信息学, AC005479.2

Abstract: Objective To investigate the key genes and their potential regulatory molecular targets of papillary thyroid carcinoma (PTC) through bioinformatics analysis, and to explore the molecular regulatory mechanism in PTC. 
Methods The gene expression profiles of PTC were retrieved and downloaded from the TCGA database, and the "Limma" software package in Rstudio was used to find out whether there was differential long non-coding RNA (lncRNA) between PTC and adjacent tissues. WGCNA was used for construction and clinical correlation analysis was performed. Enrichment analysis and annotation were performed by GSEA. 
Results After screening by the TCGA database, a total of 510 tumor tissues and 58 paracancerous tissues of PTC were included in the analysis, and a total of 58 differentially expressed lncRNAs were obtained, including 36 highly expressed genes and 22 lowly expressed genes. We used the dynamic tree cutting method to identify gene modules, set the minimum number of genes in the module to be 100, and finally obtained 11 corresponding modules. The results showed that the blue module was significantly associated with PTC. There were 34 differential lncRNAs in the blue module. Univariate and multivariate Cox regression analyses were performed on the 34 differential lncRNAs in the Blue module, and AC005479.2 was obtained. Then the receiver operating characteristic (ROC) curve was drawn for AC005479.2, with an area under the ROC curve (AUC) value of 0.838. GO and KEGG analysis revealed the potential pathways and functions of AC005479.2. The results showed that AC005479.2 might participate in cell adhesion through adipocytokine signaling pathway, MAPK signaling pathway, and cadherin binding, and positively regulate apoptosis signaling pathway, thus being involved in the pathological process of PTC. 
Conclusion There are significant differences in the expression of AC005479.2 in the thyroid tissue of PTC, patients and healthy people. The AC005479.2 gene is expected to become a biomarker gene for PTC, providing an important basis for subsequent PTC research.