Literature DB >> 8100656

Immunohistochemical study of neu protein overexpression in clinging in situ duct carcinoma of the breast.

C R De Potter1, M P Foschini, A M Schelfhout, C A Schroeter, V Eusebi.   

Abstract

The expression of neu protein in 26 cases of clinging carcinoma (CC) of the breast was investigated. A distinction is made between two types of CC: one with pleomorphic nuclei (PN) and the other with monomorphic nuclei (MN). The PN type of CC overexpresses the neu protein in almost all cases (85.7%), its cells generally exhibit abundant cytoplasm and intraluminal necrosis is frequently observed. The MN type of CC does not overexpress the neu protein, exhibits bland cytological features and shows no necrosis. It is suggested that CC with PN is related to comedo-type carcinoma, while CC with MN is the forerunner of cribriform carcinoma in situ.

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Year:  1993        PMID: 8100656     DOI: 10.1007/bf01605456

Source DB:  PubMed          Journal:  Virchows Arch A Pathol Anat Histopathol        ISSN: 0174-7398


  9 in total

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Journal:  Eur J Cancer       Date:  1992       Impact factor: 9.162

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Journal:  N Engl J Med       Date:  1988-11-10       Impact factor: 91.245

3.  The subcellular localization of the neu protein in human normal and neoplastic cells.

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Journal:  Int J Cancer       Date:  1989-12-15       Impact factor: 7.396

4.  The expression of the neu oncogene product in breast lesions and in normal fetal and adult human tissues.

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Journal:  Histopathology       Date:  1989-10       Impact factor: 5.087

5.  Long-term follow-up of in situ carcinoma of the breast with special emphasis on clinging carcinoma.

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Journal:  Semin Diagn Pathol       Date:  1989-05       Impact factor: 3.464

6.  Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene.

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Journal:  Science       Date:  1987-01-09       Impact factor: 47.728

7.  Tyrosine kinase receptor with extensive homology to EGF receptor shares chromosomal location with neu oncogene.

Authors:  L Coussens; T L Yang-Feng; Y C Liao; E Chen; A Gray; J McGrath; P H Seeburg; T A Libermann; J Schlessinger; U Francke
Journal:  Science       Date:  1985-12-06       Impact factor: 47.728

8.  Immunohistochemical demonstration of c-erbB-2 protein in mammary ductal carcinoma in situ.

Authors:  J Bartkova; D M Barnes; R R Millis; W J Gullick
Journal:  Hum Pathol       Date:  1990-11       Impact factor: 3.466

9.  c-erbB-2 expression in benign and malignant breast disease.

Authors:  B A Gusterson; L G Machin; W J Gullick; N M Gibbs; T J Powles; C Elliott; S Ashley; P Monaghan; S Harrison
Journal:  Br J Cancer       Date:  1988-10       Impact factor: 7.640

  9 in total
  6 in total

Review 1.  Are columnar cell lesions the earliest histologically detectable non-obligate precursor of breast cancer?

Authors:  Gulisa Turashvili; Malcolm Hayes; Blake Gilks; Peter Watson; Samuel Aparicio
Journal:  Virchows Arch       Date:  2008-04-24       Impact factor: 4.064

2.  [Flat epithelial neoplasia and other columnar cell lesions of the breast].

Authors:  F R Fritzsche; M Dietel; G Kristiansen
Journal:  Pathologe       Date:  2006-09       Impact factor: 1.011

3.  Molecular cytogenetic comparison of apocrine hyperplasia and apocrine carcinoma of the breast.

Authors:  C Jones; S Damiani; D Wells; R Chaggar; S R Lakhani; V Eusebi
Journal:  Am J Pathol       Date:  2001-01       Impact factor: 4.307

Review 4.  Biological features of premalignant disease in the human breast.

Authors:  D C Allred; S K Mohsin
Journal:  J Mammary Gland Biol Neoplasia       Date:  2000-10       Impact factor: 2.673

5.  The p185erbB2 protein is localized on cell organelles involved in cell motility.

Authors:  C R De Potter; J Quatacker
Journal:  Clin Exp Metastasis       Date:  1993-11       Impact factor: 5.150

Review 6.  Are Columnar Cell Lesions the Earliest Non-Obligate Precursor in the Low-Grade Breast Neoplasia Pathway?

Authors:  Sarah Strickland; Gulisa Turashvili
Journal:  Curr Oncol       Date:  2022-08-11       Impact factor: 3.109

  6 in total

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