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TGFα对胃癌细胞cyclin E和cyclin D1表达的影响
引用本文:梁卫江,张万岱,陈村龙,姚永莉,罗荣城.TGFα对胃癌细胞cyclin E和cyclin D1表达的影响[J].南方医科大学学报,2006,26(8):1255-1257.
作者姓名:梁卫江  张万岱  陈村龙  姚永莉  罗荣城
作者单位:1. 南方医科大学南方医院,肿瘤中心,广东,广州,510515
2. 南方医科大学南方医院,消化内科,广东,广州,510515
摘    要:目的 探讨TGFα对胃癌细胞cyclinE和D1表达的促进作用,为研究TGFα促胃癌发生发展机制提供重要信息。方法 ①细胞体外培养,用无血清RPMI-1640阻断法进行G0/G1期同步化,用碘化丙啶染色和流式细胞术,检测其同步化率;②细胞经G0/G1期同步化后,给予2.5%低浓度血清+RPMI-1640培养处理,以及在此基础上分别加入10、30、50μg/L TGFα处理,均作用5h;用免疫荧光染色及流式细胞术,检测细胞cyclinE和D1的表达情况。结果 细胞经无血清RPMI-1640阻断法处理,其G0/G1期的百分率由常规培养的54%上升到72%;加入TGFα处理后,细胞cyclinE和D1表达均显著高于单用低血清培养(均P〈0.001),并随TGFα剂量的增加而增加;当TGFα浓度为50μg/L时,两者的表达与单用低血清培养比,分别增加了25.18%和27.52%(均P〈0.001)。结论 TGFα可显著促进胃癌细胞cyclinE和D1的表达,从而发挥其促细胞周期进程的作用。

关 键 词:胃癌  TGFα
文章编号:1673-4254(2006)08
收稿时间:2006-02-16
修稿时间:2006年2月16日

Effect of transforming growth factor α on the expression of cyclin E and cyclin D1 in gastric carcinoma cells
LIANG Wei-jiang,ZHANG Wan-dai,CHEN Cun-long,YAO Yong-li,LUO Rong-cheng.Effect of transforming growth factor α on the expression of cyclin E and cyclin D1 in gastric carcinoma cells[J].Journal of Southern Medical University,2006,26(8):1255-1257.
Authors:LIANG Wei-jiang  ZHANG Wan-dai  CHEN Cun-long  YAO Yong-li  LUO Rong-cheng
Institution:Cancer Center, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. lwj2@nfhoc.com
Abstract:OBJECTIVE: To explore the effect of transforming growth factor alpha (TGFalpha) on the expression of cyclin E and D1 in gastric carcinoma cells. METHODS: Human gastric adenocarcinoma SGC7901 cells were cultured routinely and synchronized at G(0)/G(1) phase in serum-free RPMI-1640. The percentage of the cells at G(0)/G(1) phase was detected by propidium iodide staining and flow cytometry (FCM), and the synchronized cells were cultured in RPMI-1640 supplemented with 2.5% calf serum and treated with 10, 30, and 50 microg/L TGFalpha for 5 h. The expression of cyclin E and D1 in SGC7901 cells was detected by immunofluorescent staining and FCM. RESULTS: The percentage of the cells at G(0)/G(1) phase increased from 54% in routine culture to 72% in the serum-free RPMI-1640 culture. TGFalpha treatment of the cells synchronized at G(0)/G(1) phase induced significant increment of cyclin E and D1 expressions (P<0.001), and at the dose of TGFalpha of 50 microg/L, their expressions increased by 25.18% and 27.52%, respectively (P<0.001). CONCLUSION: TGFalpha can increase the expression of cyclin E and D1 in gastric carcinoma cells to promote their cell cycle progress.
Keywords:cyclin E  cyclin D1
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