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首页> 外文期刊>British Journal of Cancer >Microsatellite instability and loss of heterozygosity in mammary carcinoma and its probable precursors
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Microsatellite instability and loss of heterozygosity in mammary carcinoma and its probable precursors

机译:乳腺癌及其可能的前体中的微卫星不稳定性和杂合性的丧失

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Microsatellite instability is a form of genetic damage that may be due to defective mismatch repair genes and may be a marker of processes leading to malignancy. We have analysed a series of epithelial hyperplasia of usual type, carcinomas in situ and invasive and metastatic carcinomas from the mammary gland on the assumption that they represent stages in the evolution of mammary carcinoma. Eight markers on chromosomes 3p, 4q, 9p, 11p, 14q, 17p, 17q and Xq were examined for microsatellite instability and loss of heterozygosity. High rates of loss on chromosomes 17p, 17q and Xq indicate that these chromosomal arms contain genes important in mammary carcinogenesis. The rate of microsatellite instability observed in this study was uniformly low, irrespective of the lesion. This implies that microsatellite instability is not a marker of malignancy in most instances of mammary neoplasia.
机译:微卫星不稳定性是遗传损伤的一种形式,可能是由于不匹配的修复基因缺陷造成的,并且可能是导致恶性肿瘤的过程的标志。我们假设它们代表了乳腺癌发展的阶段,因此分析了一系列普通类型的上皮增生,原位癌以及乳腺浸润性和转移性癌。检查了3p,4q,9p,11p,14q,17p,17q和Xq染色体上的八个标记的微卫星不稳定性和杂合性的丧失。 17p,17q和Xq染色体上的高丢失率表明这些染色体臂含有对乳癌致癌作用很重要的基因。不论病变如何,本研究中观察到的微卫星不稳定性发生率均较低。这意味着在大多数乳腺肿瘤的情况下,微卫星不稳定性不是恶性肿瘤的标志。

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