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BTG1低表达是食管鳞状细胞癌的一个独立预后标志物。

BTG1 underexpression is an independent prognostic marker in esophageal squamous cell carcinoma.

作者信息

Sun G G, Wang Y D, Cheng Y J, Hu W N

机构信息

Department of Chemoradiotherapy, Tangshan People's Hospital, NO. 65, Shengli road, Lunan district, Tangshan, 063000, Hebei, China,

出版信息

Tumour Biol. 2014 Oct;35(10):9707-16. doi: 10.1007/s13277-014-2245-x. Epub 2014 Jun 27.

Abstract

To determine the expression and function of B cell translocation gene 1 (BTG1) in esophageal carcinoma, esophageal samples were taken from cancer lesions (n = 74) and adjacent normal tissue (n = 34) in esophageal cancer patients immediately after endoscopic biopsy. BTG1 expression was determined by immunohistochemistry and Western blotting. The effect of BTG1 overexpression was examined in vitro utilizing a human esophageal cancer cell line ECA-109 stably transfected with a recombinant lentivirus (LeBTG1 cells) and compared to empty vector-transfected controls (LeEmpty). BTG1 overexpression was verified by real-time reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot. The expression of proteins involved in cell cycle regulation (cyclin D1) and apoptosis (Bcl-2) and cell migration (MMP-9) in LeBTG1 cells was analyzed by Western blot. The effect of BTG1 overexpression on cell viability and proliferation was assessed by an MTT assay in LeBTG1 and LeEmpty cells. Flow cytometric analyses were used to evaluate the effect of BTG1 expression on cell cycle distribution and apoptosis. The migration and invasion potential of LeBTG1 cells was examined by plating cells in Matrigel-coated chambers. The level of BTG1 protein expression was found to be significantly lower in esophageal cancer tissue than normal tissues (P < 0.05). Decreased expression of BTG1 was significantly correlated with lymph node metastasis, clinical stage, and histological grade of patients with esophageal cancer (P < 0.05). Meanwhile, loss of BTG1 expression correlated significantly with poor overall survival time by Kaplan-Meier analysis (P < 0.05). The result of biological function shown that Eca-109 cell-transfected BTG1 had a lower survival fraction, higher percentage of the G0/G1 phases, higher cell apoptosis, significant decrease in migration and invasion, and lower cylin D1, Bcl-2, and MMP-9 protein expression compared with Eca-109 cell-untransfected BTG1 (P < 0.05). Reduced BTG1 expression is associated with increased disease severity, suggesting it is a negative regulator of esophageal cancer and can serve as a prognostic indicator.

摘要

为了确定B细胞易位基因1(BTG1)在食管癌中的表达及功能,在内镜活检后立即从食管癌患者的癌灶(n = 74)和癌旁正常组织(n = 34)中获取食管样本。通过免疫组织化学和蛋白质印迹法检测BTG1的表达。利用稳定转染重组慢病毒的人食管癌细胞系ECA-109(LeBTG1细胞)在体外检测BTG1过表达的影响,并与空载体转染对照(LeEmpty)进行比较。通过实时逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法验证BTG1过表达。通过蛋白质印迹法分析LeBTG1细胞中参与细胞周期调控(细胞周期蛋白D1)、凋亡(Bcl-2)和细胞迁移(基质金属蛋白酶-9)的蛋白质表达。通过MTT法评估BTG1过表达对LeBTG1和LeEmpty细胞活力和增殖的影响。采用流式细胞术分析评估BTG1表达对细胞周期分布和凋亡的影响。通过将细胞接种到基质胶包被的小室中来检测LeBTG1细胞的迁移和侵袭能力。发现食管癌组织中BTG1蛋白表达水平明显低于正常组织(P < 0.05)。BTG1表达降低与食管癌患者的淋巴结转移、临床分期和组织学分级显著相关(P < 0.05)。同时,通过Kaplan-Meier分析,BTG1表达缺失与总体生存时间较差显著相关(P < 0.05)。生物学功能结果显示,与未转染BTG1的Eca-109细胞相比,转染BTG1的Eca-109细胞存活分数更低,G0/G1期百分比更高,细胞凋亡率更高,迁移和侵袭能力显著降低,细胞周期蛋白D1、Bcl-2和基质金属蛋白酶-9蛋白表达更低(P < 0.05)。BTG1表达降低与疾病严重程度增加相关,提示其为食管癌的负调控因子,可作为预后指标。

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