Analysis of the fragile histidine triad (FHIT) gene in lobular breast cancer

被引:24
作者
Huiping, C
Jonasson, JG
Agnarsson, BA
Sigbjornsdottir, BI
Huebner, K
Ingvarsson, S
机构
[1] Univ Iceland, Dept Pathol, IS-121 Reykjavik, Iceland
[2] Thomas Jefferson Univ, Jefferson Med Coll, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
关键词
FHIT; lobular breast cancer; LOH; Fhit expression;
D O I
10.1016/S0959-8049(00)00143-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The fragile histidine triad (FHIT) gene is a candidate tumour suppressor gene in breast and other cancers. We investigated deletions within the FHIT gene in lobular breast cancer and found that 16% of cases showed loss of heterozygosity (LOH) within the gene. We compared LOH within FHIT in lobular and ductal breast tumours and found a significant association between LOH at FHIT and the ductal histological type (P < 0.001). To determine whether genomic alteration of the FHIT gene in lobular breast cancer leads to Fhit inactivation we have assessed the level of Fhit expression by immunohistochemical detection and determined that 27% (15 of 55) consecutive sporadic lobular tumours showed negative or reduced Fhit expression. A significant association was found between LOH at the FHIT gene and reduced Fhit expression in lobular and ductal tumours (P = 0.035 and P = 0.001, respectively). Thus, genetic alterations within the FHIT gene, leading to loss of Fhit protein, may play an important role in the carcinogenesis of a significant number of sporadic lobular breast cancers, even though the apparent frequency of genomic alterations within the gene is lower than in ductal breast cancer. (C) 2000 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1552 / 1557
页数:6
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