RASSF1A is a target tumor suppressor from 3p21.3 in nasopharyngeal carcinoma

被引:82
作者
Chow, LSN
Lo, KW [1 ]
Kwong, J
To, KF
Tsang, KS
Lam, CW
Dammann, R
Huang, DP
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anat & Cellular Pathol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Hong Kong Canc Inst, Sir YK Pao Ctr Canc, Shatin, Hong Kong, Peoples R China
[3] Univ Halle Wittenberg, Inst Humangenet & Med Biol, Halle An Der Saale, Germany
[4] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Hong Kong, Hong Kong, Peoples R China
关键词
RASSF1A; chromosome; 3p21.3; tumor suppressor; nasopharyngeal carcinoma;
D O I
10.1002/ijc.20079
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Deletion on the short arm of chromosome 3 is one of the most important genetic abnormalities in the tumorigenesis of nasopharyngeal carcinoma (NPC). Both physical mapping and functional studies have targeted an NPC-related tumor suppressor gene(s) to chromosome 3p21.3. We have reported recently that RASSFIA gene, located on a 120-kb minimal deletion region on 3p21.3, was frequently inactivated by promoter hypermethylation in NPC. We further confirmed that RASSFIA is the critical target tumor suppressor from 3p21.3, with the evidence that loss of expression and aberrant methylation of the other 8 candidate genes/transcripts (HYAL2, FUSI, RASSFIC, BLU, NPRL2, 101F6, PL6 and CACNA2D2) in this 120-kb region were rare in NPC samples. The contribution of RASSFIA in NPC tumorigenesis was investigated by restoring its expression in a RASSFIA deficient cell line, C666-1. Transient transfection of wild-type RASSFIA resulted in marked growth inhibition in NPC cells. Isolated stable clones expressing wild-type RASSFIA demonstrated retarded cell proliferation in vitro. Soft-agar assay also showed decreased number and sizes of colony formed in these clones. In vivo nude mice assay demonstrated the dramatic reduction of tumorigenic potential in the RASSFIA-transfected clones. Our results provide strong evidence to support RASSFIA as a target tumor suppressor gene on 3p21.3 in NPC. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:839 / 847
页数:9
相关论文
共 35 条
[1]   Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancers [J].
Agathanggelou, A ;
Dallol, A ;
Zöchbauer-Müller, S ;
Morrissey, C ;
Honorio, S ;
Hesson, L ;
Martinsson, T ;
Fong, KM ;
Kuo, MJ ;
Yuen, PW ;
Maher, ER ;
Minna, JD ;
Latif, F .
ONCOGENE, 2003, 22 (10) :1580-1588
[2]   Epigenetic inactivation of RASSF14 in lung and breast cancers and malignant phenotype suppression [J].
Burbee, DG ;
Forgacs, E ;
Zöchbauer-Müller, S ;
Shivakumar, L ;
Fong, K ;
Gao, BN ;
Randle, D ;
Kondo, M ;
Virmani, A ;
Bader, S ;
Sekido, Y ;
Latif, F ;
Milchgrub, S ;
Toyooka, S ;
Gazdar, AF ;
Lerman, MI ;
Zabarovsky, E ;
White, M ;
Minna, JD .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (09) :691-699
[3]   CACNA2D2-mediated apoptosis in NSCLC cells is associated with alterations of the intracellular calcium signaling and disruption of mitochondria membrane integrity [J].
Carboni, GL ;
Gao, BN ;
Nishizaki, M ;
Xu, K ;
Minna, JD ;
Roth, JA ;
Ji, L .
ONCOGENE, 2003, 22 (04) :615-626
[4]  
Chan ASC, 2000, CANCER RES, V60, P5365
[5]   Functional evidence for a nasopharyngeal carcinoma tumor suppressor gene that maps at chromosome 3p21.3 [J].
Cheng, Y ;
Poulos, NE ;
Lung, ML ;
Hampton, G ;
Ou, BX ;
Lerman, MI ;
Stanbridge, EJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :3042-3047
[6]  
Cheung ST, 1999, INT J CANCER, V83, P121, DOI 10.1002/(SICI)1097-0215(19990924)83:1<121::AID-IJC21>3.0.CO
[7]  
2-F
[8]  
Dammann R, 2001, CANCER RES, V61, P3105
[9]   Epigenetic inactivation of a RAS association domain family protein from the lung tumour suppressor locus 3p21.3 [J].
Dammann, R ;
Li, C ;
Yoon, JH ;
Chin, PL ;
Bates, S ;
Pfeifer, GP .
NATURE GENETICS, 2000, 25 (03) :315-319
[10]   The candidate tumor suppressor gene, RASSF1A, from human chromosome 3p21.3 is involved in kidney tumorigenesis [J].
Dreijerink, K ;
Braga, E ;
Kuzmin, I ;
Geil, L ;
Duh, FM ;
Angeloni, D ;
Zbar, B ;
Lerman, MI ;
Stanbridge, EJ ;
Minna, JD ;
Protopopov, A ;
Li, JF ;
Kashuba, V ;
Klein, G ;
Zabarovsky, ER .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (13) :7504-7509