Oral cancer overexpressed 1 (ORAOV1): A regulator for the cell growth and tumor angiogenesis in oral squamous cell carcinoma

被引:56
作者
Jiang, Lu [1 ]
Zeng, Xin [1 ]
Yang, Hanshuo [2 ,3 ]
Wang, Zhi [1 ]
Shen, Jun [1 ]
Bai, Jingping [1 ]
Zhang, Yuanyuan [1 ]
Gao, Feng [1 ]
Zhou, Min [1 ]
Chen, Qianming [1 ]
机构
[1] Sichuan Univ, State Key Lab Oral Dis, W China Coll Stomatol, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, W China Hosp, W China Med Sch, Ctr Canc, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
ORAOV1; cell growth; tumor angiogenesis; OSCC; siRNA;
D O I
10.1002/ijc.23734
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oral Cancer Overexpressed 1 (ORAOV1) is a novel gene locating at chromosome band 11q13. Recent studies have suggested its role as a candidate oncogene in oral squamous cell carcinoma (OSCC) and its prognostic value for patients with OSCC. Till now, the detailed function of ORAOV1 in OSCC has remained undefined. In this study, we have investigated the role of ORAOV1 in OSCC tumorigenesis by down-regulating its expression. Small interfering RNA (siRNA) has been applied to inhibit the expression of ORAOV1 in OSCC cells. We found that the OSCC cells with reduced ORAOV1 showed retarded cell growth in vitro and displayed inhibition in both tumor growth and tumor angiogenesis in vivo. Further analyses reveal that the retarded cell growth is associated with an increase in apoptosis involving the activation of caspase 3-dependent pathway and a cell cycle arrest at the S-phase with a downregulation of cyclin A, cyclin B1 and cdc2. The suppressed tumor growth in vivo may be attributed to synergistic effect between inhibition in cell growth and suppression of tumor angiogenesis. The latter is most likely because of a suppression of VEGF. Taken together, we demonstrate that ORAOV1 plays pivotal roles in the growth and angiogenesis of OSCC. Thus, ORAOV1 may be a novel target that could be explored to develop therapeutic strategy in OSCC management. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:1779 / 1786
页数:8
相关论文
共 30 条
[1]   Ex vivo and in vivo delivery of anti-tissue factor short interfering RNA inhibits mouse pulmonary metastasis of B16 melanoma cells [J].
Amarzguioui, Mohammed ;
Peng, Qian ;
Wiiger, Merete T. ;
Vasovic, Vlada ;
Babaie, Eshrat ;
Holen, Torgeir ;
Nesland, Jahn M. ;
Prydz, Hans .
CLINICAL CANCER RESEARCH, 2006, 12 (13) :4055-4061
[2]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[3]  
Chan TA, 2000, GENE DEV, V14, P1584
[4]   2 NEW HUMAN-TUMOR CELL-LINES DERIVED FROM SQUAMOUS-CELL CARCINOMAS OF THE TONGUE - ESTABLISHMENT, CHARACTERIZATION AND RESPONSE TO CYTO-TOXIC TREATMENT [J].
GIOANNI, J ;
FISCHEL, JL ;
LAMBERT, JC ;
DEMARD, F ;
MAZEAU, C ;
ZANGHELLINI, E ;
ETTORE, F ;
FORMENTO, P ;
CHAUVEL, P ;
LALANNE, CM ;
COURDI, A .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1988, 24 (09) :1445-1455
[5]   Positional effects of short interfering RNAs targeting the human coagulation trigger Tissue Factor [J].
Holen, T ;
Amarzguioui, M ;
Wiiger, MT ;
Babaie, E ;
Prydz, H .
NUCLEIC ACIDS RESEARCH, 2002, 30 (08) :1757-1766
[6]   High-resolution mapping of the 11q13 amplicon and identification of a gene, TAOS1, that is amplified and overexpressed in oral cancer cells [J].
Huang, X ;
Gollin, SM ;
Raja, S ;
Godfrey, TE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (17) :11369-11374
[7]   Caspase-3 and the regulation of hypoxic neuronal death by vascular endothelial growth factor [J].
Jin, K ;
Mao, XO ;
Batteur, SP ;
McEachron, E ;
Leahy, A ;
Greenberg, DA .
NEUROSCIENCE, 2001, 108 (02) :351-358
[8]  
Lewin F, 1998, CANCER-AM CANCER SOC, V82, P1367, DOI 10.1002/(SICI)1097-0142(19980401)82:7&lt
[9]  
1367::AID-CNCR21&gt
[10]  
3.0.CO