Wang Haojia, Cheng Xinhong, Zhang Bruce Xianzhuo, Wang Yong, Gao Shuo, Ding Fanghui, Song Xiaojing, Li Dandan, Ni Haixu, Luo Yang, Li Xun
The First School of Clinical Medicine, Lanzhou University, Lanzhou, China.
Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
Front Oncol. 2025 Jul 7;15:1584622. doi: 10.3389/fonc.2025.1584622. eCollection 2025.
DBC1 is a large nuclear protein that is thought to influence the development of several human cancers. However, further research has revealed that the relationship between DBC1 and the prognosis and pathological characteristics of cancer patients is controversial. The aim of this paper is to explore the significance of DBC1 in cancer through the method of meta-analysis.
A systematic search of the PubMed, Web of Science, Embase, CNKI, and Wanfang databases was conducted, resulting in the identification of 25 studies encompassing 4014 patients. The Hazard Ratio (HR) and ratio ratios (RR) were combined using STATA 14.0 software, and 95% confidence intervals (CI) were obtained to assess the association of DBC1 with prognostic and pathologic characteristics of cancer patients.
Meta-analysis of the combined results demonstrated that patients with cancer who exhibited DBC1 overexpression exhibited shorter overall survival (OS) (n = 17, HR = 1.948, 95%CI: [1.280-2.964], P = 0.002, = 88.6) and recurrence-free survival (RFS) (n = 11, HR = 2.182, 95%CI: [1.430-3.330], P = 0.000, = 87.8) rates. In terms of pathological features, elevated DBC1 expression was indicative of poor TNM stage (n = 23, RR = 1.245, 95%CI: [1.012-1.531], P = 0.038, = 79.3), distant metastasis (n = 11, RR = 1.987, 95%CI: [1.021-3.866], P = 0.043, = 63.8), and histologic grade (n = 18, RR = 1.433, 95%CI: [1.115-1.843], P = 0.005, = 79.2).
DBC1 overexpression is associated with poor survival cycle and pathologic features in cancer patients, and it has the potential to be a predictive prognostic marker for cancer. However, more high-quality prospective studies are still needed to validate our conclusions.
https://www.crd.york.ac.uk/prospero/, identifier CRD42023426104.
DBC1是一种大型核蛋白,被认为会影响多种人类癌症的发展。然而,进一步研究发现,DBC1与癌症患者的预后及病理特征之间的关系存在争议。本文旨在通过荟萃分析方法探讨DBC1在癌症中的意义。
对PubMed、Web of Science、Embase、CNKI和万方数据库进行系统检索,共纳入25项研究,涉及4014例患者。使用STATA 14.0软件合并风险比(HR)和比值比(RR),并获得95%置信区间(CI),以评估DBC1与癌症患者预后和病理特征的相关性。
综合结果的荟萃分析表明,DBC1过表达的癌症患者总生存期(OS)较短(n = 17,HR = 1.948,95%CI:[1.280 - 2.964],P = 0.002,I² = 88.6),无复发生存期(RFS)也较短(n = 11,HR = 2.182,95%CI:[1.430 - 3.330],P = 0.000,I² = 87.8)。在病理特征方面,DBC1表达升高表明TNM分期较差(n = 23,RR = 1.245,95%CI:[1.012 - 1.531],P = 0.038,I² = 79.3)、远处转移(n = 11,RR = 1.987,95%CI:[1.021 - 3.866],P = 0.043,I² = 63.8)和组织学分级较差(n = 18,RR = 1.433,95%CI:[1.115 - 1.843],P = 0.005,I² = 79.2)。
DBC1过表达与癌症患者的不良生存周期和病理特征相关,有可能成为癌症的预测性预后标志物。然而,仍需要更多高质量的前瞻性研究来验证我们的结论。