Overexpression of E2F-1 inhibits progression of gastric cancer in vitro

被引:26
作者
Xie, Yubo [1 ,2 ]
Wang, Changqing [1 ]
Li, Lei [1 ]
Ma, Yulin [1 ]
Yin, Yongshuo [1 ]
Xiao, Qiang [1 ]
机构
[1] Guangxi Med Univ, Affiliated Hosp 1, Dept Surg, Nanning 530021, Guangxi, Peoples R China
[2] Guangxi Med Univ, Affiliated Hosp 1, Dept Anesthesiol, Nanning 530021, Guangxi, Peoples R China
基金
芬兰科学院;
关键词
E2F-1; Overexpression; Gastric cancer; MGC-803; cells; Tumor progression; PROTEIN-KINASE PKR; NF-KAPPA-B; GENE-TRANSFER; E2F-1-INDUCED APOPTOSIS; TRIGGERS APOPTOSIS; CELL-LINES; C-MYC; TRANSCRIPTION; EXPRESSION; GROWTH;
D O I
10.1016/j.cellbi.2009.02.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
E2F-1 plays a critical role in cell cycle regulation and other biological processes in cells. E2F-1 mediates apoptosis and suppresses tumorigenesis in many tissue types, but there are few data available on E2F-1 expression and its relationship to tumor kinetics in gastric cancer. To gain better insight into the involvement of E2F-1 in the biological characteristics of gastric tumors, we investigated the effect of E2F-1 overexpression on the progression of gastric carcinoma cells. A gastric cancer cell line stably overexpressing E2F-1 (MGC-803/E2F-1) was established. The influence of E2F-1 overexpression on in vitro cell growth was assessed by measuring cell survival, colony formation, and cell cycle progression. The results clearly show that overexpression of E2F-1 significantly inhibits cell growth and proliferation, blocking entry into the S-phase of the cell cycle. MGC-803/E2F-1 cells also had a higher apoptotic rate than control cells. In addition, E2F-1 reduced the motility and invasion of gastric cancer cells. (c) 2009 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:640 / 649
页数:10
相关论文
共 48 条
[1]  
Atienza C, 2000, INT J MOL MED, V6, P55
[2]   p14ARF links the tumour suppressors RB and p53 [J].
Bates, S ;
Phillips, AC ;
Clark, PA ;
Stott, F ;
Peters, G ;
Ludwig, RL ;
Vousden, KH .
NATURE, 1998, 395 (6698) :124-125
[3]   DNA-binding independent cell death from a minimal proapoptotic region of E2F-1 [J].
Bell, L. A. ;
O'Prey, J. ;
Ryan, K. M. .
ONCOGENE, 2006, 25 (41) :5656-5663
[4]   Life and death decisions by E2F-1 [J].
Bell, LA ;
Ryan, KM .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (02) :137-142
[5]   E2F target genes: unraveling the biology [J].
Bracken, AP ;
Ciro, M ;
Cocito, A ;
Helin, K .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (08) :409-417
[6]   Retinoblastoma protein recruits histone deacetylase to repress transcription [J].
Brehm, A ;
Miska, EA ;
McCance, DJ ;
Reid, JL ;
Bannister, AJ ;
Kouzarides, T .
NATURE, 1998, 391 (6667) :597-601
[7]   Regulation of E2F through ubiquitin-proteasome-dependent degradation: Stabilization by the pRB tumor suppressor protein [J].
Campanero, MR ;
Flemington, EK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2221-2226
[8]   ESMO Minimum Clinical Recommendations for diagnosis, treatment and follow-up of gastric cancer [J].
Cunningham, D ;
Jost, LM ;
Purkalne, G ;
Oliveira, J .
ANNALS OF ONCOLOGY, 2005, 16 :22-23
[9]   Distinct roles for E2F proteins in cell growth control and apoptosis [J].
DeGregori, J ;
Leone, G ;
Miron, A ;
Jakoi, L ;
Nevins, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7245-7250
[10]  
Elliott MJ, 2001, CLIN CANCER RES, V7, P3590