An allelotype of papillary thyroid cancer

被引:0
|
作者
Califano, JA
Johns, MM
Westra, WH
Lango, MN
Eisele, D
Saji, M
Zeiger, MA
Udelsman, R
Koch, WM
Sidransky, D
机构
[1] JOHNS HOPKINS UNIV HOSP,DEPT OTOLARYNGOL HEAD & NECK SURG,HEAD & NECK CANC RES DIV,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV HOSP,DEPT PATHOL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV HOSP,DEPT GEN SURG,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,SCH MED,BALTIMORE,MD
[5] NYU,SCH MED,NEW YORK,NY
关键词
D O I
10.1002/(SICI)1097-0215(19961220)69:6<442::AID-IJC3>3.0.CO;2-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although papillary carcinoma accounts for approximately 70% of all thyroid cancers, preliminary studies of allelic loss have thus far not identified any areas of chomosomal deletion. We evaluated 30 papillary thyroid carcinomas for chromosomal loss/allelic imbalance by testing at least 2 microsatellite markers from every autosomal arm. Fifteen of the 30 tumors tested exhibited loss of heterozygosity/allelic imbalance (LOH/AI) at one or more loci. Chromosomal arms with frequent LOH/AI included 4q, 5p, 7p and 11p. An average of 1.1 chromosomal arms displayed LOH/AI in each individual tumor. Therefore, 4q, 5p, 7p and, to a lesser extent, 11p display significant LOH/AI in papillary thyroid cancer, which indicates the presence of putative tumor-suppressor gene loci at these chromosomal arms. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:442 / 444
页数:3
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