Anti-angiogenic and tumor-suppressive roles of candidate tumor-suppressor gene, Fibulin-2, in nasopharyngeal carcinoma

被引:92
作者
Law, E. W. L. [1 ,2 ]
Cheung, A. K. L. [1 ,2 ]
Kashuba, V. I. [3 ]
Pavlova, T. V. [3 ]
Zabarovsky, E. R. [3 ,4 ]
Lung, H. L. [1 ,2 ]
Cheng, Y. [1 ,2 ]
Chua, D. [1 ,2 ,5 ]
Kwong, D. Lai-wan [1 ,2 ]
Tsao, S. W. [6 ]
Sasaki, T. [7 ]
Stanbridge, E. J. [8 ]
Lung, M. L. [1 ,2 ]
机构
[1] Univ Hong Kong, Dept Clin Oncol, Pokfulam, Hong Kong, Peoples R China
[2] Univ Hong Kong, Ctr Canc Res, Pokfulam, Hong Kong, Peoples R China
[3] Karolinska Inst, Dept Clin Sci & Educ, Dept Microbiol Tumor & Cell Biol, Sodersjukhuset, Stockholm, Sweden
[4] Russian Acad Sci, Engelhardt Inst Mol Biol, Lab Struct & Funct Genom, Moscow, Russia
[5] Hong Kong Sanat & Hosp, Comprehens Oncol Ctr, Happy Valley, Hong Kong, Peoples R China
[6] Univ Hong Kong, Dept Anat, Pokfulam, Hong Kong, Peoples R China
[7] Univ Erlangen Nurnberg, Nikolaus Fiebiger Ctr Mol Med, Dept Expt Med 1, D-91054 Erlangen, Germany
[8] Univ Calif Irvine, Dept Microbiol & Mol Genet, Irvine, CA 92717 USA
基金
瑞典研究理事会;
关键词
anti-angiogenic; fibulin-2; nasopharyngeal carcinoma; tumor suppressor; VEGF; methylation; EXTRACELLULAR-MATRIX PROTEIN; CHROMOSOME; 3P21.3; COPY NUMBER; EXPRESSION; BREAST; CANCER; IDENTIFICATION; PROGRESSION; METASTASIS; ESOPHAGEAL;
D O I
10.1038/onc.2011.272
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Fibulin-2 (FBLN2) has been identified as a candidate tumor-suppressor gene in nasopharyngeal carcinoma (NPC). Originally identified through a chromosome 3 NotI genomic microarray screen, it shows frequent deletion or methylation in NPC. FBLN2 is located on chromosome 3p25.1 and is associated with tumor development through its important interactions with the extracellular matrix (ECM) proteins. FBLN2 encodes two isoforms. The short isoform (FBLN2S) is expressed abundantly in normal tissues, but is dramatically downregulated in NPC, while the long isoform (FBLN2L) is either not detectable or is expressed only at low levels in both normal and tumor tissues. Reintroduction of this FBLN2S inhibited cell proliferation, migration, invasion and angiogenesis in vitro. Furthermore, in vivo studies in nude mice show its expression is associated with tumor and angiogenesis suppression. FBLN2-associated angiogenesis occurs via concomitant downregulation of vascular endothelial growth factor and matrix metalloproteinase 2. This study provides compelling evidence that FBLN2S has an important tumor-suppressive and anti-angiogenic role in NPC. Oncogene (2012) 31, 728-738; doi:10.1038/onc.2011.272; published online 11 July 2011
引用
收藏
页码:728 / 738
页数:11
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