Graduate School of Dalian Medical University, Dalian Medical University, Dalian 116044, China.
Department of General Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou 213000, China.
Biomed Res Int. 2021 Jan 29;2021:6622437. doi: 10.1155/2021/6622437. eCollection 2021.
Cell division cycle-associated protein-3 (CDCA3) contributes to the regulation of the cell cycle. CDCA3 plays an important role in the carcinogenesis of various cancers; however, the association between CDCA3 expression, prognosis of patients, and immune infiltration in the tumor microenvironment is still unknown. Here, we demonstrated that CDCA3 was differentially expressed between the tumor tissues and corresponding normal tissues using in silico analysis in the ONCOMINE and Tumor Immune Estimation Resource (TIMER) databases. We analyzed the relationship between the expression of CDCA3 and prognosis of patients with hepatocellular carcinoma (HCC) using the Kaplan-Meier plotter database and Gene Expression Profiling Interactive Analysis (GEPIA). Furthermore, we determined the prognostic value of CDCA3 expression using univariate and multivariate analyses. We observed that CDCA3 expression closely correlated with immune infiltration and gene markers of infiltrating immune cells in the TIMER database. CDCA3 was highly expressed in the tumor tissues than in the adjacent normal tissues in various cancers, including HCC. Increased expression of CDCA3 was accompanied by poorer overall survival (OS), relapse-free survival (RFS), progression-free survival (PFS), and disease-specific survival (DSS). The correlation between CDCA3 expression and OS and disease-free survival (DFS) was also studied using GEPIA. CDCA3 expression was associated with the levels of immune cell infiltration and was positively correlated with tumor purity. Moreover, CDCA3 expression was associated with gene markers such as , , , and from exhausted T cells, , , and from T cells, and and located on the surface of Tregs. Thus, we demonstrated that CDCA3 may be a potential target and biomarker for the management and diagnosis of HCC.
细胞分裂周期相关蛋白 3(CDCA3)参与细胞周期的调控。CDCA3 在各种癌症的发生发展中发挥着重要作用;然而,CDCA3 表达与肿瘤微环境中患者预后和免疫浸润的关系尚不清楚。在这里,我们通过 ONCOMINE 和 Tumor Immune Estimation Resource(TIMER)数据库中的计算分析,证明了 CDCA3 在肿瘤组织和相应正常组织之间的差异表达。我们使用 Kaplan-Meier plotter 数据库和 Gene Expression Profiling Interactive Analysis(GEPIA)分析了 CDCA3 表达与肝细胞癌(HCC)患者预后的关系。此外,我们通过单因素和多因素分析确定了 CDCA3 表达的预后价值。我们观察到 CDCA3 在 TIMER 数据库中的表达与免疫浸润和浸润免疫细胞的基因标志物密切相关。在各种癌症中,包括 HCC,CDCA3 在肿瘤组织中的表达高于相邻的正常组织。CDCA3 表达的增加伴随着总生存期(OS)、无复发生存期(RFS)、无进展生存期(PFS)和疾病特异性生存期(DSS)的降低。我们还使用 GEPIA 研究了 CDCA3 表达与 OS 和无病生存期(DFS)的相关性。CDCA3 表达与免疫细胞浸润水平相关,并与肿瘤纯度呈正相关。此外,CDCA3 表达与耗竭 T 细胞的基因标记物 、T 细胞的基因标记物 、和 以及 Tregs 表面的基因标记物 、和 呈正相关。因此,我们证明 CDCA3 可能是 HCC 管理和诊断的潜在靶点和生物标志物。