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[建立浸润性乳腺癌的细胞遗传学和形态学进展模型。女性乳腺恶性和癌前肿瘤的比较基因组杂交(CGH)]

[Establishing a cytogenetic and morphological progression models of invasive breast cancer. Comparative genomic hybridization (CGH) in malignant and premalignant tumors of the female breast].

作者信息

Bürger H, Poremba C, Diallo R, Dockhorn-Dworniczak B, Böcker W

机构信息

Gerhard-Domagk-Institut für Pathologie, Westfälische Wilhelmsuniversität Münster.

出版信息

Pathologe. 2000 Sep;21(5):375-82. doi: 10.1007/s002920000404.

DOI:10.1007/s002920000404
PMID:11092010
Abstract

Ductal carcinoma in situ of the female breast and lobular carcinoma in situ are regarded as precursor lesions of invasive breast cancer. We used comparative genomic hybridization to analyze the genetic relationship between these two types of lesion and invasive breast cancer. The series included 166 patients with ductal or lobular carcinoma in situ and invasive breast cancer. Our results reflect the broad heterogeneity of morphologically different subtypes of invasive and noninvasive breast cancer. The data also provide evidence of multiple genetic pathways of invasive breast cancer associated with different morphological subtypes. In conclusion, we propose a combined model of morphological-genetic progression with various parallel pathways in the pathogenesis of invasive breast cancer.

摘要

女性乳腺导管原位癌和小叶原位癌被视为浸润性乳腺癌的前驱病变。我们采用比较基因组杂交技术分析这两种病变与浸润性乳腺癌之间的遗传关系。该系列研究纳入了166例患有导管或小叶原位癌以及浸润性乳腺癌的患者。我们的结果反映了浸润性和非浸润性乳腺癌形态学不同亚型的广泛异质性。这些数据还为与不同形态学亚型相关的浸润性乳腺癌的多种遗传途径提供了证据。总之,我们提出了一种在浸润性乳腺癌发病机制中具有多种平行途径的形态学 - 遗传学进展联合模型。

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1
[Establishing a cytogenetic and morphological progression models of invasive breast cancer. Comparative genomic hybridization (CGH) in malignant and premalignant tumors of the female breast].[建立浸润性乳腺癌的细胞遗传学和形态学进展模型。女性乳腺恶性和癌前肿瘤的比较基因组杂交(CGH)]
Pathologe. 2000 Sep;21(5):375-82. doi: 10.1007/s002920000404.
2
Clonal relationship between closely approximated low-grade ductal and lobular lesions in the breast: a molecular study of 10 cases.乳腺中紧密相邻的低级别导管和小叶病变之间的克隆关系:10例分子研究
Am J Clin Pathol. 2009 Dec;132(6):871-6. doi: 10.1309/AJCP7AK1VWFNMCSW.
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Genetic relation of lobular carcinoma in situ, ductal carcinoma in situ, and associated invasive carcinoma of the breast.乳腺小叶原位癌、导管原位癌及相关浸润性癌的遗传关系。
Mol Pathol. 2000 Jun;53(3):118-21. doi: 10.1136/mp.53.3.118.
4
Molecular evidence for progression of microglandular adenosis (MGA) to invasive carcinoma.微腺性腺病(MGA)进展为浸润性癌的分子证据。
Am J Surg Pathol. 2009 Apr;33(4):496-504. doi: 10.1097/PAS.0b013e31818af361.
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Genetic changes in intraductal breast cancer detected by comparative genomic hybridization.通过比较基因组杂交检测导管内乳腺癌的基因变化。
Am J Pathol. 1997 Apr;150(4):1465-71.
6
High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancer.在因乳腺癌遗传风险而接受预防性乳房切除的女性中,癌前病变的患病率较高。
J Clin Oncol. 2003 Jan 1;21(1):41-5. doi: 10.1200/JCO.2003.02.137.
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Premalignant and in situ breast disease: biology and clinical implications.乳腺癌前病变及原位病变:生物学特性与临床意义
Ann Intern Med. 2005 Sep 20;143(6):446-57. doi: 10.7326/0003-4819-143-6-200509200-00009.
8
Carcinoma in situ of the female breast. A clinico-pathological, immunohistological, and DNA ploidy study.女性乳腺原位癌。一项临床病理、免疫组织化学及DNA倍体研究。
APMIS Suppl. 2003(108):1-67.
9
Flow cytometric DNA analysis of breast cancers with predominance of carcinoma in situ: a comparison of the premalignant and malignant components.以原位癌为主的乳腺癌的流式细胞术DNA分析:癌前成分与恶性成分的比较
Clin Cancer Res. 1995 Aug;1(8):881-8.
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Definition of precancerous and high-risk mammary lesions.癌前和高危乳腺病变的定义。
Can J Surg. 1985 May;28(3):248-51.

引用本文的文献

1
[The significance of "normal tissue" in the development of breast cancer: new concepts of early carcinogenesis].[“正常组织”在乳腺癌发生发展中的意义:早期致癌作用的新概念]
Pathologe. 2006 Sep;27(5):319-25. doi: 10.1007/s00292-006-0857-7.
2
[Concepts and problems of lobular neoplasia].[小叶瘤变的概念与问题]
Pathologe. 2006 Sep;27(5):373-80. doi: 10.1007/s00292-006-0859-5.
3
Twist overexpression induces in vivo angiogenesis and correlates with chromosomal instability in breast cancer.Twist过表达可诱导体内血管生成,并与乳腺癌中的染色体不稳定相关。
Cancer Res. 2005 Dec 1;65(23):10801-9. doi: 10.1158/0008-5472.CAN-05-0712.