解剖学报 ›› 2023, Vol. 54 ›› Issue (4): 434-444.doi: 10.16098/j.issn.0529-1356.2023.04.009

• 肿瘤生物学 • 上一篇    下一篇

爪蟾驱动蛋白样蛋白2靶蛋白在肝细胞癌的表达及临床预后的意义

安韶光1 马俊杰1 张浩轩2,3 陆进2,3*   

  1. 1.蚌埠医学院临床医学院2020级; 2.数字医学与智慧健康安徽省重点实验室; 3.人体解剖学教研室,安徽 蚌埠 233030
  • 收稿日期:2022-05-10 修回日期:2022-07-19 出版日期:2023-08-06 发布日期:2023-08-06
  • 通讯作者: 陆进 E-mail:0100197@bbmc.edu.cn
  • 基金资助:
    安徽省教育厅自然科学研究重点项目;2021年教育部产学合作协同育人项目

Expression and prognostic significance of targeting protein for xenopus kinesin-like protein 2 in hepatocellular carcinoma

AN  Shao-guang1 MA  Jun-jie1  ZANG  Hao-xuan2,3 LU  Jin2,3*   

  1. 1.Grade 2020 of Clinical Medical College; 2.Anhui Key Laboratory of Computational Medicine and Intelligent Health; 3.Department of Human Anatomy, Bengbu Medical College, Anhui Bengbu 233030,China
  • Received:2022-05-10 Revised:2022-07-19 Online:2023-08-06 Published:2023-08-06
  • Contact: LU Jin E-mail:0100197@bbmc.edu.cn

摘要:

目的  分析爪蟾驱动蛋白样蛋白2靶蛋白(TPX2)在肝细胞癌(HCC)的表达及其临床预后的意义。   方法  首先,分别利用UALCAN、K-M Plot以及HPA数据库分析TPX2在HCC的表达水平、生存预后及其相关性;再次,利用TIMER、GEPIA和SangerBox数据库分析TPX2的免疫细胞浸润以及与TP53突变相关性和突变景观图;最后,通过HCCDB数据库分析在HCC中TPX2的共表达基因及其预后价值,并对共表达基因进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析。   结果  TPX2在HCC高表达且不利于患者的总体生存(OS)、疾病特异性生存(DSS)、无进展生存(PFS)和无复发生存(RFS);同时,TPX2在HCC组织与肿瘤细胞纯度和多种免疫细胞(B细胞、CD4+T以及 CD8+T等)显著相关;并且,TPX2在HCC中的表达水平与TP53突变显著相关。TPX2对HCC患者1年、3年和5年OS预后诊断的受试者工作特征(ROC)曲线下面积(AUC)分别是0.73,95% CI(0.669~0.79)、0.668,95% CI(0.604~0.732)和0.654,95% CI(0.574~0.734)。TPX2的共表达基因在HCC均不利于患者的OS;其GO功能主要富集在有丝分裂与核分裂、微管细胞骨架以及微管运动等,KEGG主要富集在细胞周期、卵母细胞减数分裂以及p53信号等通路上,且对HCC患者1年、3年和5年OS预后诊断的ROC曲线下面积AUC分别是0.801,95% CI(0.745~0.856)、0.725,95% CI(0.667~0.786)和0.711,95% CI(0.635~0.788)。   结论  TPX2与HCC的发生密切相关,不利于HCC患者的生存预后,可作为HCC诊断与预后的生物标志物。

关键词: 爪蟾驱动蛋白样蛋白2靶蛋白, 无病生存, 肝细胞癌, 生物信息学, 数据库分析

Abstract:

 Objective  To analyze the expression of targeting protein for xenopus kinesin-like protein 2(TPX2) in hepatocellular carcinoma (HCC) and its clinical prognostic significance.    Methods  First, the expression levels, survival prognosis and correlation of TPX2 in HCC were analyzed using UALCAN, K-PLOT and HPA databases. Secondly, the TIMER, GEPIA, and SangerBox databases were used to analyze the immune cell infiltration of TPX2, its correlation with TP53 mutation, and the mutation landscape map. Finally, the co-expressed genes of TPX2 in HCC and their prognostic value were analyzed by HCCDB database, and the co-expressed genes were analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genome (KEGG) were analyzed by the HCCDB database.    Results  TPX2 was highly expressed in HCC and was not conducive to overall survival(OS), disease-specific survival(DSS), progression-free survival(PFS), and recurrence free survival(RFS) of HCC patients; and its presence in HCC was significantly correlated with tumor cell purity and multiple immune cells (B cells, CD4+T, and CD8+T, etc.); Furthermore, the expression level of TPX2 in HCC was significantly correlated with TP53 mutation. The area under curve(AUC) under receiver operating characteristic(ROC) curve of TPX2 for the 1-year, 3-year and 5-year OS prognostic diagnosis in HCC patients was 0.73, 95% CI (0.669-0.79), 0.668, 95% CI (0.604-0.732) and 0.654,5% CI (0.574-0.734), respectively. Co-expressed genes of TPX2 were not conducive to OS of patient; its GO function was mainly enriched in mitosis and nuclear division, microtubule cytoskeleton, and KEGG was mainly enriched in cell cycle, oocyte meiosis and p53 signaling pathways, and AUC of the 1-year, 3-year and 5-year OS prognostic for HCC patients was 0.801, 95% CI (0.745-0.856), 0.725, 95% CI (0.667-0.786) and 0.711, 95% CI (0.635~0.788).      Conclusion  TPX2 is closely related to the occurrence of HCC, which is not conducive to the survival and prognosis of HCC patients, and can be served as a biomarker for the diagnosis and prognosis of HCC.

Key words:

中图分类号: