Heightened expression of CTCF in breast cancer cells is associated with resistance to apoptosis

被引:85
作者
Docquier, F
Farrar, D
D'Arcy, V
Chernukhin, I
Robinson, AF
Loukinov, D
Vatolin, S
Pack, S
Mackay, A
Harris, RA
Dorricott, H
O'Hare, MJ
Lobanenkov, V
Klenova, E
机构
[1] Univ Essex, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
[2] Univ Oxford, Dept Biochem, Genet Unit, Oxford OX1 2JD, England
[3] UCL, LICR, Breast Canc Lab, London, England
[4] UCL, Dept Physiol, London, England
[5] NIAID, Mol Pathol Sect, Immunopathol Lab, NIH, Rockville, MD 20852 USA
关键词
D O I
10.1158/0008-5472.CAN-03-3498
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CTCF is a candidate tumor suppressor gene encoding a multifunctional transcription factor. Surprisingly for a tumor suppressor, the levels of CTCF in breast cancer cell lines and tumors were found elevated compared with breast cell lines with finite life span and normal breast tissues. In this study, we aimed to investigate the possible cause for this increase in CTCF content and in particular to test the hypothesis that up-regulation of CTCF may be linked to resistance of breast cancer cells to apoptosis. For this purpose, apoptotic cell death was monitored following alterations of CTCF levels induced by transient transfection and conditional knockdown of CTCF in various cell lines. We observed apoptotic cell death in all breast cancer cell lines examined following CTCF down-regulation. In addition, overexpression of CTCF partially protected cells from apoptosis induced by overexpression of Bax or treatment with sodium butyrate. To elucidate possible mechanisms of this phenomenon, we used a proteomics approach and observed that levels of the proapoptotic protein, Bax, were increased following CTCF down-regulation in MCF7 cells. Taken together, these results suggest that in some cellular contexts CTCF shows antiapoptotic characteristics, most likely exerting its functions through regulation of apoptotic genes. We hypothesize that CTCF overexpression may have evolved as a compensatory mechanism to protect breast cancer cells from apoptosis, thus providing selective survival advantages to these cells. The observations reported in this study may lead to development of therapies based on selective reduction of CTCF in breast cancer cells.
引用
收藏
页码:5112 / 5122
页数:11
相关论文
共 52 条
[11]   Induction of cell cycle progression and acceleration of apoptosis are two separable functions of c-Myc: Transrepression correlates with acceleration of apoptosis [J].
Conzen, SD ;
Gottlob, K ;
Kandel, ES ;
Khanduri, P ;
Wagner, AJ ;
O'Leary, M ;
Hay, N .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (16) :6008-6018
[12]   Differential expression and phosphorylation of CTCF, a c-myc transcriptional regulator, during differentiation of human myeloid cells [J].
Delgado, MD ;
Chernukhin, IV ;
Bigas, A ;
Klenova, EM ;
León, J .
FEBS LETTERS, 1999, 444 (01) :5-10
[13]   Downregulation of p21waf/cip-1 mediates apoptosis of human hepatocellular carcinoma cells in response to interferon-γ [J].
Detjen, KM ;
Murphy, D ;
Welzel, M ;
Farwig, K ;
Wiedenmann, B ;
Rosewicz, S .
EXPERIMENTAL CELL RESEARCH, 2003, 282 (02) :78-89
[14]   Quantitative analysis of BRCA1 and BRCA2 mRNA expression in sporadic breast carcinomas and its relationship with clinicopathological characteristics [J].
Egawa, C ;
Miyoshi, Y ;
Taguchi, T ;
Tamaki, Y ;
Noguchi, S .
JAPANESE JOURNAL OF CANCER RESEARCH, 2001, 92 (06) :624-630
[15]   Proliferation, cell cycle and apoptosis in cancer [J].
Evan, GI ;
Vousden, KH .
NATURE, 2001, 411 (6835) :342-348
[16]  
Filippova GN, 2002, CANCER RES, V62, P48
[17]  
Filippova GN, 1996, MOL CELL BIOL, V16, P2802
[18]  
Filippova GN, 1998, GENE CHROMOSOME CANC, V22, P26, DOI 10.1002/(SICI)1098-2264(199805)22:1<26::AID-GCC4>3.3.CO
[19]  
2-W
[20]  
Fraizer G, 2004, INT J ONCOL, V24, P461