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Neuroendocrine differentiation in carcinoma of the breast. Tyramide signal amplification discloses chromogranin A-positive tumour cells in more breast tumours than previously realized.

Authors :
Bofin AM
Qvigstad G
Waldum C
Waldum HL
Source :
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica [APMIS] 2002 Sep; Vol. 110 (9), pp. 658-64.
Publication Year :
2002

Abstract

The aim of the study was to determine if, by means of tyramide signal amplification (TSA), the presence of chromogranin A (CgA)-positive tumour cells could be demonstrated in breast cancer cases found to be negative by conventional immunohistochemical staining. Sections from 44 cases of breast cancer (28 infiltrating ductal carcinomas, 2 lobular carcinomas, 4 ductal carcinomas in situ (DCIS), 7 lobular carcinomas in situ (LCIS), and 3 mucinous carcinomas) were stained for CgA by conventional immunohistochemical methods and by immunohistochemistry with TSA. The sections were also histologically graded and their oestrogen receptor (ER), progesterone receptor (PgR) and HER-2 oncogene status was recorded. Five of the tumours showed CgA-positive staining with the polyclonal antibody 430 with conventional methods. Thirty cases showed CgA-immunoreactive tumour cells after immunohistochemical staining with the polyclonal antibody 430 with TSA. However, eight of these also showed faint staining with the negative control antibody X0936 with TSA. One case showed immunopositivity for CgA using a monoclonal antibody without tyramide amplification and only a further two cases were positive when TSA was applied. The presence of CgA appears to be associated with a lower histological grade and may be more often found in oestrogen receptor-positive tumours.

Details

Language :
English
ISSN :
0903-4641
Volume :
110
Issue :
9
Database :
MEDLINE
Journal :
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
Publication Type :
Academic Journal
Accession number :
12529020
Full Text :
https://doi.org/10.1034/j.1600-0463.2002.1100910.x