Effect of DEK gene silencing on proliferation and apoptosis in human oral squamous cell carcinoma PCI-37 B cells

被引:0
作者
Zhao, Tengfei [1 ]
Huang, Shaohui [1 ]
Kou, Yurong [1 ,2 ]
Liu, Jie [3 ]
Gao, Hua [1 ]
Zheng, Chen [1 ]
Wang, Yunjing [1 ]
Wang, Zechen [1 ]
Sun, Changfu [1 ]
机构
[1] China Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Shenyang, Liaoning, Peoples R China
[2] China Med Univ, Dept Oral Biol, Shenyang, Liaoning, Peoples R China
[3] China Med Univ, Ctr Expt & Technol, Shenyang, Liaoning, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2017年 / 10卷 / 02期
基金
中国国家自然科学基金;
关键词
DEK; oral squamous cell carcinoma; gene silencing; proliferation; apoptosis; PROTOONCOGENE PROTEIN DEK; MAMMALIAN CHROMATIN; DNA; BINDING; IDENTIFICATION; EXPRESSION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oral squamous cell carcinoma (OSCC) is one the oral diseases of which are major causes of cancer-related death. Despite the development of advanced technologies in clinical and experimental oncology in recent years, the 5-year survival rate is still low. Therefore the identification of novel OSCC related molecules and the discovery of new makers and drug targets are essential. The human DEK gene has been implicated as an oncogene in OSCC, which has been proved to participate in several critical biological signaling pathways including the expression of protein and mRNA. This study demonstrates that DEK is highly expressed in OSCC cells compared to normal tissue cells. Additionally, inhibition of DEK gene expression can effectively inhibit the proliferation of oral cancer cells. Also the inhibition of DEK gene arrest cells in G0/G1 phase and then impact proliferation and differentiation, thus suggesting that DEK may participate in the procedure of OSCC growth and progression.
引用
收藏
页码:2370 / 2376
页数:7
相关论文
共 25 条
[1]   SAP - a putative DNA-binding motif involved in chromosomal organization [J].
Aravind, L ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :112-114
[2]   DEK Regulates Hematopoietic Stem Engraftment and Progenitor Cell Proliferation [J].
Broxmeyer, Hal E. ;
Kappes, Ferdinand ;
Mor-Vaknin, Nirit ;
Legendre, Maureen ;
Kinzfogl, John ;
Cooper, Scott ;
Hangoc, Giao ;
Markovitz, David M. .
STEM CELLS AND DEVELOPMENT, 2012, 21 (09) :1449-1454
[3]   DEK expression is controlled by E2F and deregulated in diverse tumor types [J].
Carro, Maria Stella ;
Spiga, Fabio Mario ;
Quarto, Micaela ;
Di Ninni, Valentina ;
Volorio, Sara ;
Alcalay, Myriam ;
Muller, Heiko .
CELL CYCLE, 2006, 5 (11) :1202-1207
[4]   p300/CBP-associated factor drives DEK into interchromatin granule clusters [J].
Cleary, J ;
Sitwala, KV ;
Khodadoust, MS ;
Kwok, RPS ;
Mor-Vaknin, N ;
Cebrat, M ;
Cole, PA ;
Markovitz, DM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (36) :31760-31767
[5]  
Grottke C, 2000, INT J CANCER, V88, P535, DOI 10.1002/1097-0215(20001115)88:4<535::AID-IJC4>3.3.CO
[6]  
2-M
[7]   The distribution of the DEK protein in mammalian chromatin [J].
Hu, Hong-gang ;
Scholten, Ingo ;
Gruss, Claudia ;
Knippers, Rolf .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 358 (04) :1008-1014
[8]  
Hua Y, 2009, CHINESE SCI C, V33, P434
[9]   Progress in studies on the DEK protein and its involvement in cellular apoptosis [J].
Hua Ying ;
Hu HongGang ;
Peng XiangLei .
SCIENCE IN CHINA SERIES C-LIFE SCIENCES, 2009, 52 (07) :637-642
[10]   Phosphorylation by protein kinase CK2 changes the DNA binding properties of the human chromatin protein DEK [J].
Kappes, F ;
Damoc, C ;
Knippers, R ;
Przybylski, M ;
Pinna, LA ;
Gruss, C .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (13) :6011-6020