Infrequent mutation of TRAIL receptor 2 (TRAIL-R2/DR5) in transitional cell carcinoma of the bladder with 8p21 loss of heterozygosity

被引:22
作者
Adams, J
Cuthbert-Heavens, D
Bass, S
Knowles, MA
机构
[1] St James Univ Hosp, Canc Res UK Clin Ctr, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, Can Res UK Mutat Detect Facil, Leeds LS9 7TF, W Yorkshire, England
关键词
transitional cell carcinoma; 8p21; mutation; tumour necrosis factor-related apoptosis-inducing ligand receptor 2;
D O I
10.1016/j.canlet.2004.06.052
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Loss of heterozygosity (LOH) on 8p is a frequent event in many cancers and is often associated with more aggressive disease. Tumour necrosis factor-related apoptosis inducing ligand (TRAIL) receptor 2 (TRAIL-R2) also known as TNFRSF10B (tumour necrosis factor receptor (TNFR) super family 10b) or KILLER/DR5, a member of the TNFR family, is a promising candidate tumour suppressor gene at 8p21-22. Mutations in this gene have been identified in non-small cell lung cancer, head and neck cancer, breast cancer and non-Hodgkin's lymphoma. We carried out mutation analysis of TRAIL-R2 in bladder cancer cell lines and in primary bladder tumours. One novel protein truncating mutation was identified in a bladder cancer cell line. Our results suggest that if TRAIL-R2 is the target of LOH events in these cancers, inactivation of the remaining allele is by a mechanism other than mutation. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:137 / 144
页数:8
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