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10号染色体长臂缺失在滤泡性甲状腺肿瘤进展中的作用

Deletions of the long arm of chromosome 10 in progression of follicular thyroid tumors.

作者信息

Zedenius J, Wallin G, Svensson A, Bovèe J, Höög A, Bäckdahl M, Larsson C

机构信息

Department of Surgery, Karolinska Hospital, Stockholm, Sweden.

出版信息

Hum Genet. 1996 Mar;97(3):299-303. doi: 10.1007/BF02185758.

Abstract

Previous studies of follicular thyroid tumors have shown loss of heterozygosity (LOH) on the short arm of chromosome 3 in carcinomas, and on chromosome 10 in atypical adenomas and carcinomas, but not in common adenomas. We studied LOH on these chromosomal arms in 15 follicular thyroid carcinomas, 19 atypical follicular adenomas and 6 anaplastic (undifferentiated) carcinomas. Deletion mapping of chromosome 10 using 15 polymorphic markers showed that 15 (37.5%) of the tumors displayed LOH somewhere along the long arm. Thirteen of these tumors showed deletions involving the telomeric part of chromosome 10q, distal to D10S187. LOH on chromosome 3p was found in 8 (20%) cases. Seven of these also showed LOH on chromosome 10q. In eight cases LOH was seen on chromosome 10q but not 3p. In comparison, the retinoblastoma gene locus at chromosome 13q showed LOH in 22% of the tumors. Most of these also had deletions on chromosome 10q. The results indicate that a region at the telomeric part of 1Oq may be involved in progression of follicular thyroid tumors.

摘要

以往对滤泡性甲状腺肿瘤的研究表明,在癌中3号染色体短臂存在杂合性缺失(LOH),在非典型腺瘤和癌中10号染色体存在杂合性缺失,但在常见腺瘤中未出现。我们研究了15例滤泡性甲状腺癌、19例非典型滤泡性腺瘤和6例间变性(未分化)癌中这些染色体臂上的杂合性缺失情况。使用15个多态性标记对10号染色体进行缺失图谱分析显示,15个(37.5%)肿瘤在长臂的某个位置出现了杂合性缺失。其中13个肿瘤显示缺失涉及10q染色体的端粒部分,位于D10S187远端。在8例(20%)病例中发现3p染色体存在杂合性缺失。其中7例在10q染色体上也存在杂合性缺失。8例在10q染色体上出现杂合性缺失,但3p染色体上未出现。相比之下,13q染色体上的视网膜母细胞瘤基因位点在22%的肿瘤中出现杂合性缺失。其中大多数在10q染色体上也有缺失。结果表明,10q端粒部分的一个区域可能与滤泡性甲状腺肿瘤的进展有关。

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