Cancer Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Tianjin Medical University, Tianjin, 300203, China.
Curr Med Sci. 2020 Feb;40(1):85-94. doi: 10.1007/s11596-020-2150-z. Epub 2020 Mar 13.
Abundant studies have been conducted to identify how B-cell translocation gene 1 protein (BTG1) gene affects the differentiation, proliferation, metastasis of cancer cells, and how it further regulates the generation or development of diseases to influence the prognosis of patients. However, the data from single research were not powerful enough. The correlations between BTG1 expression and mechanisms of tumorigenesis or prognosis of patients are still in controversial. Our system review and meta-analysis provided a complete explanation about the association between BTG1 expression and clinicopathological features or prognosis of patients, which further laid a foundation for future research on BTG1. Fifteen eligible studies consisting of 1992 participants were included. We uncovered that BTG1 expression in solid tumors was associated with lymph node status (RR=0.66, 95% CI: 0.58-0.75, P=0.142), TMN stage status (RR=2.13, 95% CI: 1.71-2.65, P=0.001), T category (RR=1.90, 95% CI: 1.20-3.00, P=0.000), histological differentiation (RR=1.91, 95% CI: 1.55-2.37, P=0.012), vascular invasion (RR=0.90, 95% CI: 0.57-1.41, P=0.001). BTG1 low expression was significantly associated with overall survival (OS) (HR=0.47, 95% CI: 0.38-0.67, P=0.000). It concluded that BTG1 possessed the potential value for future research and could be recommended as a significant biomarker in solid tumor.
大量研究已经证实 B 细胞易位基因 1 蛋白(BTG1)基因如何影响癌细胞的分化、增殖、转移,以及如何进一步调节疾病的发生或发展,从而影响患者的预后。然而,单一研究的数据并不充分。BTG1 表达与肿瘤发生机制或患者预后的相关性仍存在争议。我们的系统评价和荟萃分析提供了关于 BTG1 表达与患者临床病理特征或预后之间关联的完整解释,为进一步研究 BTG1 奠定了基础。共有 15 项符合条件的研究,包括 1992 名参与者,纳入我们的研究。我们发现实体瘤中 BTG1 的表达与淋巴结状态(RR=0.66,95%CI:0.58-0.75,P=0.142)、TMN 分期(RR=2.13,95%CI:1.71-2.65,P=0.001)、T 分期(RR=1.90,95%CI:1.20-3.00,P=0.000)、组织学分化(RR=1.91,95%CI:1.55-2.37,P=0.012)和血管侵犯(RR=0.90,95%CI:0.57-1.41,P=0.001)有关。BTG1 低表达与总生存期(OS)显著相关(HR=0.47,95%CI:0.38-0.67,P=0.000)。综上所述,BTG1 具有未来研究的潜力,可以作为实体瘤中一种有意义的生物标志物。