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BRCA1蛋白保守末端区域的截短与高度增殖性遗传性乳腺癌相关。

Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers.

作者信息

Sobol H, Stoppa-Lyonnet D, Bressac-de-Paillerets B, Peyrat J P, Kerangueven F, Janin N, Noguchi T, Eisinger F, Guinebretiere J M, Jacquemier J, Birnbaum D

机构信息

Department of Genetic Oncology and Laboratory of Tumor Biology, Paoli-Calmettes Institute, INSERM U 119, France.

出版信息

Cancer Res. 1996 Jul 15;56(14):3216-9.

PMID:8764110
Abstract

The existence of two subgroups of BRCA1-associated breast cancer (BC) families has been recently posited: the first with highly proliferating tumors, and the second composed of cases with a low proliferation rate. Our aim was to test whether the proliferation rate of BRCA1-associated breast cancers was affected by the site of the germ line mutation in the BRCA1 gene. We analyzed the distribution of the mitotic index, a histoprognostic grade component shown to segregate in families, matching for germ line mutation location in a series of 28 breast cancers from 20 kindreds. We observed a prevalence of highly proliferating tumors when the mutation occurs in the two terminal conserved domains of the BRCA1 protein, ie., in the amino and carboxyl termini (P = 0.0024). Our data provide evidence for a genotype-phenotype correlation and along with their strong conservation during evolution argue for the importance of these two regions in the control of mammary cell growth.

摘要

最近有人提出,与BRCA1相关的乳腺癌(BC)家族存在两个亚组:第一个亚组的肿瘤具有高度增殖性,第二个亚组则由增殖率低的病例组成。我们的目的是测试BRCA1相关乳腺癌的增殖率是否受BRCA1基因种系突变位点的影响。我们分析了有丝分裂指数的分布情况,有丝分裂指数是一种组织预后分级成分,已证实在家族中可分离,我们对来自20个家族的28例乳腺癌进行了分析,这些病例的种系突变位置相匹配。我们观察到,当突变发生在BRCA1蛋白的两个末端保守结构域,即氨基末端和羧基末端时,高度增殖性肿瘤的发生率较高(P = 0.0024)。我们的数据为基因型与表型的相关性提供了证据,并且鉴于它们在进化过程中的高度保守性,证明了这两个区域在控制乳腺细胞生长中的重要性。

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