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乳腺癌旁正常组织中的杂合性缺失

Loss of heterozygosity in normal tissue adjacent to breast carcinomas.

作者信息

Deng G, Lu Y, Zlotnikov G, Thor A D, Smith H S

机构信息

Geraldine Brush Cancer Research Institute, California Pacific Medical Center, 2330 Clay Street, San Francisco, CA 94619, USA.

出版信息

Science. 1996 Dec 20;274(5295):2057-9. doi: 10.1126/science.274.5295.2057.

DOI:10.1126/science.274.5295.2057
PMID:8953032
Abstract

Loss of heterozygosity (LOH) was detected in morphologically normal lobules adjacent to breast cancers. The most frequent aberration was at chromosome 3p22-25; of ten cases with this LOH in the carcinoma, six displayed the same LOH in adjacent normal lobules. This suggests that in a subset of sporadic breast cancers, a tumor suppresser gene at 3p22-25 may be important in initiation or early progression of tumorigenesis. Among sixteen breast cancers with LOH at 17p13.1 and five breast cancers with LOH at 11p15.5, one case each displayed the same LOH in adjacent normal lobules. Thus the molecular heterogeneity that characterizes invasive breast cancers may occur at the earliest detectable stages of progression.

摘要

在乳腺癌旁形态学正常的小叶中检测到杂合性缺失(LOH)。最常见的畸变位于染色体3p22 - 25;在癌组织中有这种LOH的10个病例中,6个在相邻正常小叶中显示相同的LOH。这表明在一部分散发性乳腺癌中,位于3p22 - 25的一个肿瘤抑制基因可能在肿瘤发生的起始或早期进展中起重要作用。在16例17p13.1存在LOH的乳腺癌和5例11p15.5存在LOH的乳腺癌中,各有1例在相邻正常小叶中显示相同的LOH。因此,侵袭性乳腺癌所特有的分子异质性可能在最早可检测到的进展阶段就已出现。

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1
Loss of heterozygosity in normal tissue adjacent to breast carcinomas.乳腺癌旁正常组织中的杂合性缺失
Science. 1996 Dec 20;274(5295):2057-9. doi: 10.1126/science.274.5295.2057.
2
Loss of heterozygosity is detected at chromosomes 1p35-36 (NB), 3p25 (VHL), 16p13 (TSC2/PKD1), and 17p13 (TP53) in microdissected apocrine carcinomas of the breast.在乳腺微切割顶泌汗腺癌中,在染色体1p35 - 36(神经母细胞瘤)、3p25(VHL)、16p13(TSC2/PKD1)和17p13(TP53)检测到杂合性缺失。
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Patterns of allelic loss on chromosome 17 in sporadic breast carcinomas detected by fluorescent-labeled microsatellite analysis.通过荧光标记微卫星分析检测散发性乳腺癌中17号染色体上等位基因缺失模式。
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Mutation at chromosome 11q23 in human non-familial breast cancer: a microdissection microsatellite analysis.人类非家族性乳腺癌11号染色体q23位点的突变:一项显微切割微卫星分析
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Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer.8号染色体短臂杂合性缺失与乳腺癌的侵袭性行为相关。
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Accumulation of genetic alterations in brain metastases of sporadic breast carcinomas is associated with reduced survival after metastasis.散发性乳腺癌脑转移中基因改变的积累与转移后生存期缩短有关。
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Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast.乳腺微切割导管癌组织学进展过程中11号染色体p15区域杂合性缺失
Am J Pathol. 1998 Jul;153(1):271-8. doi: 10.1016/S0002-9440(10)65568-X.
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Loss of heterozygosity at chromosome 6q in preinvasive and early invasive breast carcinomas.原位及早期浸润性乳腺癌6号染色体长臂杂合性缺失
Br J Cancer. 1997;75(9):1324-9. doi: 10.1038/bjc.1997.224.

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