Frequency of fibroblast growth factor receptor 3 mutations in sporadic tumours

被引:0
|
作者
Kathryn Sibley
Peter Stern
Margaret A Knowles
机构
[1] ICRF Clinical Centre,
[2] St. James's University Hospital,undefined
[3] Leeds,undefined
[4] CRC Immunology Group,undefined
[5] Paterson Institute for Cancer Research,undefined
[6] Manchester,undefined
来源
Oncogene | 2001年 / 20卷
关键词
FGFR3; mutation; tumour;
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学科分类号
摘要
Mutations in FGFR3 have been identified in several tumour types including bladder carcinoma, cervical carcinoma, and multiple myeloma. In bladder carcinoma, we recently identified FGFR3 mutations in 41% of tumours, making this the most frequently mutated putative oncogene identified in bladder cancer to date. We have now investigated the frequency of FGFR3 mutation in a panel of 125 tumours and 13 cell lines from various other organs. We analysed the mutation hotspots in exons 7, 10 and 15 by direct DNA sequencing, and found one mutation in exon 7 (S249C) in 1/28 (3.5%) cervical tumours. Mutations were not detected in stomach, rectum, colon, prostate, ovarian, breast, brain, or renal tumours, nor were they found in any of the cell lines included in this study. We conclude that FGFR3 is commonly mutated in bladder carcinoma and only rarely in cervical carcinoma. Several tumour types appear not to possess any mutations in FGFR3, suggesting that these mutations are important only in the development of certain types of tumour.
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页码:4416 / 4418
页数:2
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