Fan Hai-Hua, Zhang Hai-Jun
Department of Oncology, The Affiliated Tumor Hospital of Nantong University, Nantong, Jiangsu, China.
Department of Oncology, The Affiliated Zhongda Hospital of Southeast University, Medical School of Southeast University, Nanjing, Jiangsu, China.
Front Oncol. 2024 Mar 11;14:1333702. doi: 10.3389/fonc.2024.1333702. eCollection 2024.
The purpose of this study was to investigate the potential of EVA1A as a prognostic biomarker for Colorectal cancer (CRC).
The study utilized public databases to analyze the difference in mRNA expression between CRC tumor tissues and adjacent normal tissues. Additionallymunohistochemical staining was performed on 90 paired tissue samples to detect EVA1A expression. The relationship between EVA1A and clinicopathological features was examined, and a Kaplan-Meier survival analysis was conducted. Univariate and multivariate Cox analyses were employed to identify prognostic factors affecting the overall survival (OS) of CRC patients.
The analysis revealed a significant increase in mRNA expression in CRC tumor cells compared to normal controls from public databases (P< 0.05). Immunohistochemical staining further confirmed a significant upregulation of EVA1A expression in CRC tissues (P< 0.05). High EVA1A expression was associated with age, pathological M stage, total tumor stage, and Carbohydrate antigen CA19-9 (CA19-9). Kaplan-Meier analysis demonstrated a significant association between high EVA1A expression and poor OS. Univariate and multivariate analysis identified EVA1A as an independent risk factor for CRC prognosis.
The study suggests that EVA1A is increased in CRC tumor tissues and may serve as a potential biomarker for poor prognosis in CRC.
本研究旨在探讨EVA1A作为结直肠癌(CRC)预后生物标志物的潜力。
本研究利用公共数据库分析CRC肿瘤组织与相邻正常组织之间mRNA表达的差异。此外,对90对组织样本进行免疫组织化学染色以检测EVA1A表达。研究了EVA1A与临床病理特征之间的关系,并进行了Kaplan-Meier生存分析。采用单因素和多因素Cox分析来确定影响CRC患者总生存期(OS)的预后因素。
分析显示,与公共数据库中的正常对照相比,CRC肿瘤细胞中的mRNA表达显著增加(P<0.05)。免疫组织化学染色进一步证实CRC组织中EVA1A表达显著上调(P<0.05)。EVA1A高表达与年龄、病理M分期、肿瘤总分期和糖类抗原CA19-9(CA19-9)相关。Kaplan-Meier分析表明,EVA1A高表达与较差的OS显著相关。单因素和多因素分析确定EVA1A是CRC预后的独立危险因素。
该研究表明,CRC肿瘤组织中EVA1A升高,可能是CRC预后不良的潜在生物标志物。