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原发性乳腺癌7号染色体上的基因改变图谱

Genetic alteration mapping on chromosome 7 in primary breast cancer.

作者信息

Bièche I, Khodja A, Driouch K, Lidereau R

机构信息

Laboratoire d'Oncogénétique, Centre René Huguenin, 35 rue Dailly, F-92211 St-Cloud, France.

出版信息

Clin Cancer Res. 1997 Jun;3(6):1009-16.

PMID:9815778
Abstract

Alterations of chromosome 7 are among the most frequent cytogenetic abnormalities found in human breast carcinoma. We examined genetic changes on chromosome 7 in 113 primary human breast tumors, using both microsatellite and restriction fragment length polymorphism/variable number of tandem repeats polymorphism markers mapping to the long arm (15 markers) and the short arm (8 markers). Allelic imbalance at 1 or more loci was observed in 50 (44%) of 113 tumors on the long arm of chromosome 7 and in 41 (36%) tumors on the short arm. Genetic changes of one arm were significantly associated with alterations of the other arm. The 50 7q-altered tumor DNAs exclusively showed a loss of heterozygosity (LOH), 23 (46%) at all informative loci tested on 7q and 27 (54%) at some loci (interstitial and/or telomeric deletions on 7q). The pattern of LOH of these 27 tumors enabled us to identify 3 distinct consensus regions of deletions on 7q, only 1 of which (7q31 region) has already been described in breast cancer. Among the 41 7p-altered tumor DNAs, 32 had a gain and/or loss of the entire short arm of chromosome 7. Fourteen tumor DNAs showed an allelic gain, and 18 tumor DNAs showed a LOH at each locus on the short arm. The other 9 7p-altered tumors showing partial random alterations of chromosome 7p revealed no common altered regions. This is the first report of an association between alterations of DNA sequences on chromosome 7p and breast cancer. The results suggest that tumor suppressor genes are present on the long arm of chromosome 7 and are associated with breast tumorigenesis. Moreover, the frequent loss or gain of a whole copy of chromosome 7p suggests the involvement of a gene dosage effect of this chromosomal arm in the pathogenesis of breast cancer.

摘要

7号染色体的改变是人类乳腺癌中最常见的细胞遗传学异常之一。我们使用映射到长臂(15个标记)和短臂(8个标记)的微卫星以及限制性片段长度多态性/可变串联重复序列多态性标记,检测了113例原发性人类乳腺肿瘤中7号染色体的基因变化。在113例肿瘤中,50例(44%)在7号染色体长臂上的1个或更多位点观察到等位基因失衡,41例(36%)在短臂上观察到等位基因失衡。一条臂的基因变化与另一条臂的改变显著相关。50个7q改变的肿瘤DNA仅显示杂合性缺失(LOH),在7q上所有检测的信息位点中有23个(46%)出现LOH,在某些位点(7q上的间质和/或端粒缺失)有27个(54%)出现LOH。这27个肿瘤的LOH模式使我们能够在7q上识别出3个不同的缺失共识区域,其中只有1个区域(7q31区域)已在乳腺癌中被描述。在41个7p改变的肿瘤DNA中,32个有7号染色体整个短臂的增加和/或缺失。14个肿瘤DNA显示等位基因增加,18个肿瘤DNA在短臂的每个位点显示LOH。其他9个7p改变的肿瘤显示7p染色体部分随机改变,未发现共同的改变区域。这是关于7号染色体短臂上DNA序列改变与乳腺癌之间关联的首次报道。结果表明,肿瘤抑制基因存在于7号染色体长臂上,并与乳腺肿瘤发生相关。此外,7号染色体短臂频繁的全拷贝丢失或增加表明该染色体臂的基因剂量效应参与了乳腺癌的发病机制。

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