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Basic transcription factor 3 is involved in gastric cancer development and progression

Basic transcription factor 3 is involved in gastric cancer development and progression

作     者:Qi Liu Jian-Ping Zhou Bin Li Zhong-Cheng Huang Hong-Yu Dong Guang-Yi Li Ke Zhou Shao-Lin Nie 

作者机构:Department of Anorectal Surgery People's Hospital of Hunan Province the First Affiliated Hospital of Hunan Normal University Department of Elderly Surgery the Second Xiangya Hospital of Central South University Department of Tumor Chemotherapy Xiangya Hospital of Central South University Department of Gastrointestinal Surgery Hunan Provincial Tumor Hospital theAffiliated Tumor Hospital of Central South University 

出 版 物:《World Journal of Gastroenterology》 (世界胃肠病学杂志(英文版))

年 卷 期:2013年第19卷第28期

页      面:4495-4503页

核心收录:

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

基  金:Supported by Science and Technology Project of Hunan Province  China  No. 2013FJ3151 

主  题:Basic transcription factor 3 Gastric cancer Small interfering RNA Proliferation Apoptosis Cell cycle 

摘      要:AIM: To further analyse cancer involvement of basic transcription factor 3 (BTF3) after detection of its upregulation in gastric tumor samples. METHODS: BTF3 transcription rates in human gastric tumor tissue samples (n = 20) and adjacent normal tissue (n = 18) specimens as well as in the gastric cancer cell lines AGS, SGC-7901, MKN-28, MKN-45 and MGC803 were analyzed via quantitative real-time polymerase chain reaction. The effect of stable BTF3 silencing via infection with a small interfering RNA (siRNA)-BTF3 expressing lentivirus on SGC-7901 cells was measured via Western blotting analysis, proliferation assays, cell cycle and apoptosis profiling by flow cytometry as well as colony forming assays with a Cellomic Assay System. RESULTS: A significant higher expression of BTF3 mRNA was detected in tumors compared to normal gastric tissues (P 0.01), especially in section tissues from female patients compared to male patients, and all tested gastric cancer cell lines expressed high levels of BTF3. From days 1 to 5, the relative proliferation rates of stable BTF3-siRNA transfected SGC7901 cells were 82%, 70%, 57%, 49% and 44% compared to the control, while the percentage of cells arrested in the G 1 phase was significantly decreased (P = 0.000) and the percentages of cells in the S (P = 0.031) and G 2 /M (P = 0.027) phases were significantly increased. In addition, the colony forming tendency was significantly decreased (P = 0.014) and the apoptosis rate increased from 5.73% to 8.59% (P = 0.014) after BTF3 was silenced in SGC7901 cells. CONCLUSION: BTF3 expression is associated with enhanced cell proliferation, reduced cell cycle regulation and apoptosis and its silencing decreased colony forming and proliferation of gastric cancer cells.

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