Identification of a candidate tumor suppressor gene RHOBTB1 located at a novel allelic loss region 10q21 in head and neck cancer

被引:29
作者
Beder, LB
Gunduz, M
Ouchida, M
Gunduz, E
Sakai, A
Fukushima, K
Nagatsuka, H
Ito, S
Honjo, N
Nishizaki, K
Shimizu, K
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Mol Genet, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med & Dent, Dept Otolaryngol, Okayama 7008558, Japan
[3] Okayama Univ, Grad Sch Med & Dent, Dept Oral Med & Pathol, Okayama 7008558, Japan
关键词
10q21; RHOBTB1; EGR2; LOH analysis; RT-PCR;
D O I
10.1007/s00432-005-0033-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Aims of the study are to narrow-down the hotspot region on 10q21 defined by previous genome-wide loss of heterozygosity (LOH) analysis in head and neck squamous cell carcinomas (HNSCC) and to define candidate tumor suppressor genes (TSG) concerned with 10q21. Materials and methods: LOH analysis was carried out with ten polymorphic microsatellite markers. Expression analysis was performed by semi-quantitative RT-PCR, and mutation analysis by PCR and direct sequencing. Results: LOH analysis on 10q21 in 52 HNSCC indicated distinctive and frequent allelic loss at D10S589 (42%). Among flanking genes, we found the RHOBTB1 gene as a candidate TSG, since an intragenic marker demonstrated the highest LOH (44%). Expression analysis revealed down-regulation of RHOBTB1 mRNA in 37% of tumors. Interestingly, all the five tumors that showed decreased expression of RHOBTB1 were accompanied with LOH, supporting the haploinsufficiency and class 2 TSG characteristics of RHOBTB1. No pathogenic mutation of RHOBTB1 was found. Furthermore, another gene within the region, EGR2, was also taken under scope. LOH frequencies around the EGR2 gene were relatively low (23 and 33%). Albeit semi-quantitative expression analysis of EGR2 demonstrated downregulation in 45% of tumor samples, no relation was found between the expression levels and LOH status. Conclusion: Frequent allelic loss and decreased expression of RHOBTB1 suggested that this gene has a role in tumorigenesis of a subset of HNSCC.
引用
收藏
页码:19 / 27
页数:9
相关论文
共 32 条
[1]   Rho GTPases have diverse effects on the organization of the actin filament system [J].
Aspenström, P ;
Fransson, Å ;
Saras, J .
BIOCHEMICAL JOURNAL, 2004, 377 :327-337
[2]   Genome-wide analyses on loss of heterozygosity in head and neck squamous cell carcinomas [J].
Beder, LB ;
Gunduz, M ;
Ouchida, M ;
Fukushima, K ;
Gunduz, E ;
Ito, S ;
Sakai, A ;
Nagai, N ;
Nishizaki, K ;
Shimizu, K .
LABORATORY INVESTIGATION, 2003, 83 (01) :99-105
[3]   HUMAN P53 IS PHOSPHORYLATED BY P60-CDC2 AND CYCLIN-B-CDC2 [J].
BISCHOFF, JR ;
FRIEDMAN, PN ;
MARSHAK, DR ;
PRIVES, C ;
BEACH, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4766-4770
[4]   The role of Rho GTPases in disease development [J].
Boettner, B ;
Van Aelst, L .
GENE, 2002, 286 (02) :155-174
[5]   New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase AKT pathway [J].
Cantley, LC ;
Neel, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4240-4245
[6]   Frequent loss of heterozygosity on chromosome 10q in muscle-invasive transitional cell carcinomas of the bladder [J].
Cappellen, D ;
deMedina, SGD ;
Chopin, D ;
Thiery, JP ;
Radvanyi, F .
ONCOGENE, 1997, 14 (25) :3059-3066
[7]   All in the family: the BTB/POZ, KRAB, and SCAN domains [J].
Collins, T ;
Stone, JR ;
Williams, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (11) :3609-3615
[8]   Modeling stochastic gene expression: Implications for haploinsufficiency [J].
Cook, DL ;
Gerber, LN ;
Tapscott, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15641-15646
[9]  
Gasparotto D, 1999, INT J CANCER, V84, P432, DOI 10.1002/(SICI)1097-0215(19990820)84:4<432::AID-IJC18>3.0.CO
[10]  
2-#