Lentivirus-mediated gene silencing of beta-catenin inhibits growth of human tongue cancer cells

被引:7
作者
Duan, Ying
Fan, Mingwen [1 ]
机构
[1] Wuhan Univ, Key Lab Breeding Base Basic Sci Stomatol Hubei MO, Sch & Hosp Stomatol, Wuhan 430079, Peoples R China
关键词
beta-catenin; gene therapy; RNA interference; tongue cancer; COLON-CANCER; IN-VITRO; EXPRESSION; ACTIVATION; CARCINOMA; PATHWAY; PROLIFERATION; ACCUMULATION; COMPLEX; MICE;
D O I
10.1111/j.1600-0714.2011.01007.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BACKGROUND: Beta-catenin is one of the key components of Wnt signaling pathway. Increased level of this protein has been proved to be associated with enhanced cellular proliferation and the development of many kinds of cancers. But its role in the carcinogenesis in human tongue squamous cell carcinoma, one of the most common carcinomas of the human oral cavity, remains poorly characterized. METHODS: In this study, we used lentivirus-mediated RNA interference (RNAi) targeted against beta-catenin to determine the effects of decreasing the high constitutive level of this protein in human tongue carcinoma cell line Tca8113. RESULTS: Our studies demonstrated that RNAi directly against beta-catenin markedly decreased beta-catenin gene expression and inhibited cellular proliferation as reflected in the reduced growth of tongue cancer cells both in vitro and in nude mice. CONCLUSIONS: RNA interference (RNAi) targeting against beta-catenin can induce cell growth suppression of tongue cancer and may have the potential as a therapeutic modality to treat human tongue cancer. J Oral Pathol Med (2011) 40: 643-650
引用
收藏
页码:643 / 650
页数:8
相关论文
共 31 条
[11]   Mutations of the APC, beta-catenin, and axin 1 genes and cytoplasmic accumulation of beta-catenin in oral squamous cell carcinoma [J].
Iwai, S ;
Katagiri, W ;
Kong, C ;
Amekawa, S ;
Nakazawa, M ;
Yura, Y .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2005, 131 (12) :773-782
[12]   CK1ε Is Required for Breast Cancers Dependent on β-Catenin Activity [J].
Kim, So Young ;
Dunn, Ian F. ;
Firestein, Ron ;
Gupta, Piyush ;
Wardwell, Leslie ;
Repich, Kara ;
Schinzel, Anna C. ;
Wittner, Ben ;
Silver, Serena J. ;
Root, David E. ;
Boehm, Jesse S. ;
Ramaswamy, Sridhar ;
Lander, Eric S. ;
Hahn, William C. .
PLOS ONE, 2010, 5 (02)
[13]   Coincident expression of β-catenin and cyclin D1 in endometrial stromal tumors and related high-grade sarcomas [J].
Kurihara, Shuichi ;
Oda, Yoshinao ;
Ohishi, Yoshihiro ;
Kaneki, Eisuke ;
Kobayashi, Hiroaki ;
Wake, Norio ;
Tsuneyoshi, Masazumi .
MODERN PATHOLOGY, 2010, 23 (02) :225-234
[14]   Epidermal growth factor receptor regulates β-catenin location, stability, and transcriptional activity in oral cancer [J].
Lee, Chien-Hsing ;
Hung, Hsing-Wen ;
Hung, Pei-Hsin ;
Shieh, Yi-Shing .
MOLECULAR CANCER, 2010, 9
[15]   Lentivirus-mediated silencing of Tiam1 gene influences multiple functions of a human colorectal cancer cell line [J].
Liu, Li ;
Zhang, Qingling ;
Zhang, Yanfei ;
Wang, Shuang ;
Ding, Yanqing .
NEOPLASIA, 2006, 8 (11) :917-U24
[16]   Cutaneous cancer stem cell maintenance is dependent on β-catenin signalling [J].
Malanchi, Ilaria ;
Peinado, Hector ;
Kassen, Deepika ;
Hussenet, Thomas ;
Metzger, Daniel ;
Chambon, Pierre ;
Huber, Marcel ;
Hohl, Daniel ;
Cano, Amparo ;
Birchmeier, Walter ;
Huelsken, Joerg .
NATURE, 2008, 452 (7187) :650-U12
[17]   β-Catenin is involved in alterations in mitochondrial activity in non-transformed intestinal epithelial and colon cancer cells [J].
Mezhybovska, M. ;
Yudina, Y. ;
Abhyankar, A. ;
Sjolander, A. .
BRITISH JOURNAL OF CANCER, 2009, 101 (09) :1596-1605
[18]   Convergence of Wnt, β-catenin, and cadherin pathways [J].
Nelson, WJ ;
Nusse, R .
SCIENCE, 2004, 303 (5663) :1483-1487
[19]   Crosstalk between NF-κB/p65 and β-catenin/TCF4/p300 signalling pathway through alterations in GSK-3β expression during trans-differntiation of endometrial carcinoma cells [J].
Saegusa, M. ;
Hashimura, M. ;
Kuwata, T. ;
Hamano, M. ;
Okayasu, I. .
JOURNAL OF PATHOLOGY, 2007, 213 (01) :35-45
[20]   Cadherin Switching and Activation of β-Catenin Signaling Underlie Proinvasive Actions of Calcitonin-Calcitonin Receptor Axis in Prostate Cancer [J].
Shah, Girish V. ;
Muralidharan, Anbalagan ;
Gokulgandhi, Mitan ;
Soan, Kamal ;
Thomas, Shibu .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (02) :1018-1030