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乳腺癌进展的遗传分析。

Genetic analysis of breast cancer progression.

作者信息

Dairkee S H, Smith H S

机构信息

Geraldine Brush Cancer Research Institute, California Pacific Medical Center, San Francisco 94115, USA.

出版信息

J Mammary Gland Biol Neoplasia. 1996 Apr;1(2):139-51. doi: 10.1007/BF02013638.

DOI:10.1007/BF02013638
PMID:10887488
Abstract

At the histological level, breast tumors display a variety of morphologic lesions which suggest the existence of an increasingly aberrant pathway of intermediate steps leading to the invasive primary tumor and its metastatic dissemination. In order to obtain direct evidence for this presumed progression, underlying genetic changes must be identified. Analyses of primary breast tumors have revealed a large number of dominant and recessive gene alterations encompassing several cellular attributes and activities. It is quite likely that some of these alterations are of a causal nature and thus enable the tumor to attain distinctive malignant phenotypes, such as, dysregulated proliferation, invasion, angiogenesis, and ability to metastasize. Considerable heterogeneity has been observed in the sequence of acquisition of these genetic changes, which is substantiated by recent comparative analyses between carefully microdissected preinvasive and invasive tumor. The data are evaluated here in the context of existing models of breast cancer progression. Implication and prospects for translational application to the clinic are also discussed.

摘要

在组织学层面,乳腺肿瘤呈现出多种形态学病变,这表明存在一条越来越异常的中间步骤途径,导致原发性浸润性肿瘤及其转移扩散。为了获得这种假定进展的直接证据,必须识别潜在的基因变化。对原发性乳腺肿瘤的分析揭示了大量显性和隐性基因改变,涵盖了多种细胞特性和活动。其中一些改变很可能具有因果性质,从而使肿瘤能够获得独特的恶性表型,如增殖失调、侵袭、血管生成和转移能力。在这些基因变化的获得顺序中观察到了相当大的异质性,最近对仔细显微切割的侵袭前和侵袭性肿瘤进行的比较分析证实了这一点。本文在现有乳腺癌进展模型的背景下对这些数据进行了评估。还讨论了其在临床转化应用中的意义和前景。

相似文献

1
Genetic analysis of breast cancer progression.乳腺癌进展的遗传分析。
J Mammary Gland Biol Neoplasia. 1996 Apr;1(2):139-51. doi: 10.1007/BF02013638.
2
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Breast Cancer Res. 2015 Jul 25;17(1):98. doi: 10.1186/s13058-015-0607-y.
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Breast Cancer Res Treat. 1999 May;55(2):127-36. doi: 10.1023/a:1006188129423.
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引用本文的文献

1
Modeling the effect of tumor size in early breast cancer.模拟早期乳腺癌中肿瘤大小的影响。
Ann Surg. 2005 Feb;241(2):309-18. doi: 10.1097/01.sla.0000150245.45558.a9.

本文引用的文献

1
ErbB2 activation and signal transduction in normal and malignant mammary cells.正常及恶性乳腺细胞中的ErbB2激活与信号转导
J Mammary Gland Biol Neoplasia. 1996 Apr;1(2):199-206. doi: 10.1007/BF02013643.
2
P53, apoptosis, and breast cancer.P53、细胞凋亡与乳腺癌
J Mammary Gland Biol Neoplasia. 1996 Apr;1(2):163-75. doi: 10.1007/BF02013640.
3
Allelic loss on a chromosome 17 in ductal carcinoma in situ of the breast.乳腺导管原位癌中17号染色体上的等位基因缺失。
Cancer Res. 1993 Jul 1;53(13):2947-9.
4
Ligand-specific activation of HER4/p180erbB4, a fourth member of the epidermal growth factor receptor family.表皮生长因子受体家族的第四个成员HER4/p180erbB4的配体特异性激活。
Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1746-50. doi: 10.1073/pnas.90.5.1746.
5
Nm23 and breast cancer metastasis.Nm23与乳腺癌转移
Breast Cancer Res Treat. 1993;25(2):175-87. doi: 10.1007/BF00662142.
6
Maspin, a serpin with tumor-suppressing activity in human mammary epithelial cells.Maspin,一种在人乳腺上皮细胞中具有肿瘤抑制活性的丝氨酸蛋白酶抑制剂。
Science. 1994 Jan 28;263(5146):526-9. doi: 10.1126/science.8290962.
7
Amplification and overexpression of cyclin D1 in breast cancer detected by immunohistochemical staining.通过免疫组织化学染色检测乳腺癌中细胞周期蛋白D1的扩增和过表达。
Cancer Res. 1994 Apr 1;54(7):1812-7.
8
A candidate tumor suppressor gene in human breast cancers.人类乳腺癌中的一个候选肿瘤抑制基因。
Cancer Res. 1994 Mar 15;54(6):1393-6.
9
Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization.通过比较基因组杂交技术检测和定位乳腺癌中扩增的DNA序列
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2156-60. doi: 10.1073/pnas.91.6.2156.
10
Amplification of c-myc but not of c-erbB-2 is associated with high proliferative capacity in breast cancer.
Cancer Res. 1993 Apr 15;53(8):1956-61.