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乳腺癌进展过程中染色体8p臂的等位基因缺失。

Allelic loss of chromosomal arm 8p in breast cancer progression.

作者信息

Anbazhagan R, Fujii H, Gabrielson E

机构信息

Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Am J Pathol. 1998 Mar;152(3):815-9.

Abstract

Loss of heterozygosity (LOH) of chromosomal arm 8p has been reported to occur at high frequency for a number of common forms of human cancer, including breast cancer. The objectives of this study were to define the regions on this chromosomal arm that are likely to contain breast cancer tumor suppressor genes and to determine when loss of chromosomal arm 8p occurs during breast cancer progression. For mapping the tumor suppressor gene loci, we evaluated 60 cases of infiltrating ductal cancer for allelic loss using 14 microsatellite markers mapped to this chromosomal arm and found LOH of 8p in 36 (60%) of the tumors. Whereas most of these tumors had allelic loss at all informative markers, five tumors had partial loss of 8p affecting two nonoverlapping regions. LOH for all but one of the tumors with 8p loss involved the region between markers D8S560 and D8S518 at 8p21.3-p23.3, suggesting that this is the locus of a breast cancer tumor suppressor gene. We then studied LOH of 8p in 38 cases of ductal carcinoma in situ (DCIS) with multiple individually microdissected tumor foci evaluated for each case. LOH of 8p was found in 14 of the DCIS cases (36%), including 6 of 16 cases of low histological grade and 8 of 22 cases of intermediate or high histological grade. In four of these DCIS cases, 8p LOH was seen in some but not all of the multiple tumor foci examined. These data suggest that during the evolution of these tumors, LOH of 8p occurred after loss of other chromosomal arms that were lost in all tumor foci. Thus, LOH of 8p, particularly 8p21.3-p23, is a common genetic alteration in infiltrating and in situ breast cancer. Although 8p LOH is common even in low histological grade DCIS, this allelic loss often appears to be preceded by loss of other alleles in the evolution of breast cancer.

摘要

据报道,包括乳腺癌在内的多种常见人类癌症中,染色体8p臂杂合性缺失(LOH)的发生率很高。本研究的目的是确定该染色体臂上可能包含乳腺癌抑癌基因的区域,并确定在乳腺癌进展过程中8p染色体臂缺失发生的时间。为了定位抑癌基因位点,我们使用14个定位于该染色体臂的微卫星标记,评估了60例浸润性导管癌的等位基因缺失情况,发现36例(60%)肿瘤存在8p LOH。虽然这些肿瘤中的大多数在所有信息性标记处都存在等位基因缺失,但有5例肿瘤8p部分缺失,影响两个不重叠区域。除1例8p缺失肿瘤外,其余所有肿瘤的LOH均涉及8p21.3 - p23.3区域的D8S560和D8S518标记之间,这表明该区域是乳腺癌抑癌基因的位点。然后,我们研究了38例导管原位癌(DCIS)的8p LOH情况,对每例病例的多个单独显微切割肿瘤灶进行了评估。在14例DCIS病例(36%)中发现了8p LOH,包括16例低组织学分级病例中的6例以及22例中或高组织学分级病例中的8例。在这些DCIS病例中的4例中,在所检查的多个肿瘤灶中,部分但并非全部出现了8p LOH。这些数据表明,在这些肿瘤的演变过程中,8p LOH发生在所有肿瘤灶中其他染色体臂缺失之后。因此,8p LOH,特别是8p21.3 - p23区域的LOH,是浸润性和原位乳腺癌中常见的基因改变。尽管8p LOH在低组织学分级的DCIS中也很常见,但在乳腺癌的演变过程中,这种等位基因缺失似乎常常先于其他等位基因的缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/158c/1858406/bfb56cd24aba/amjpathol00015-0189-a.jpg

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