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与组织学类型和分级相关的乳腺导管内肿瘤的基因改变模式。

Pattern of gene alterations in intraductal breast neoplasms associated with histological type and grade.

作者信息

Tsuda H, Fukutomi T, Hirohashi S

机构信息

Pathology Division and Department of Surgery, National Cancer Center Research Institute and Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104, Japan.

出版信息

Clin Cancer Res. 1995 Mar;1(3):261-7.

PMID:9815981
Abstract

To reveal any association between the histological type and grade of intraductal breast neoplasms and the manner of accumulation of gene alterations, eight types of gene alterations, i.e., loss of heterozygosity (LOH) on chromosomal arms 16p, 16q, 17p, 17q, and 18q, amplification of the c-erbB-2 and hst-1/int-2 genes, and mutation of the p53 gene, were examined by Southern blot analysis or single-strand conformation polymorphism analysis in a total of 60 cases of intraductal breast cancer and 18 nonmalignant proliferative lesions. Among the histological types and three histological grade groups of intraductal carcinomas, the gene alterations which occurred most frequently were LOH on 16q alone in non-comedo type and Grade 1, alterations of c-erbB-2, 17p, and 16q in comedo type and Grade 2, and alterations of 17q and p53 as well as those of 16q, 17p, and c-erbB-2 in Grade 3. LOH on 16q and 18q was frequent in intraductal carcinoma of the intracystic papillary type, whereas LOH on 18q alone was detected in 27% of papillomas. Among intraductal carcinomas, the mean number of gene alterations was largest in comedo type and Grade 3, whereas it was smallest in non-comedo type and Grade 1. It was possible that LOH on 18q and 16q was involved frequently in papillary tumori-genesis and acquisition of malignant phenotype, respectively, whereas most of the other gene alterations were involved in acquisition of aggressive biological properties by intraductal carcinoma cells. It was also possible that the phenotype of breast neoplasms was determined by the combination of gene alterations at a relatively early developmental stage.

摘要

为了揭示乳腺导管内肿瘤的组织学类型和分级与基因改变累积方式之间的任何关联,通过Southern印迹分析或单链构象多态性分析,对总共60例乳腺导管癌和18例非恶性增殖性病变检测了8种基因改变,即染色体臂16p、16q、17p、17q和18q上的杂合性缺失(LOH)、c-erbB-2和hst-1/int-2基因的扩增以及p53基因的突变。在导管内癌的组织学类型和三个组织学分级组中,最常发生的基因改变是在非粉刺型和1级中单独出现的16q上的LOH,在粉刺型和2级中c-erbB-2、17p和16q的改变,以及在3级中17q和p53以及16q、17p和c-erbB-2的改变。16q和18q上的LOH在囊内乳头状型导管内癌中很常见,而在27%的乳头状瘤中检测到单独的18q上的LOH。在导管内癌中,基因改变的平均数量在粉刺型和3级中最大,而在非粉刺型和1级中最小。有可能18q和16q上的LOH分别频繁参与乳头状肿瘤发生和恶性表型的获得,而大多数其他基因改变参与导管癌细胞侵袭性生物学特性的获得。乳腺肿瘤的表型也有可能在相对早期发育阶段由基因改变的组合决定。

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