Expression of amphiregulin and epidermal growth factor receptor in human breast cancer: analysis of autocriny and stromal-epithelial interactions

Citation
L. Ma et al., Expression of amphiregulin and epidermal growth factor receptor in human breast cancer: analysis of autocriny and stromal-epithelial interactions, J PATHOLOGY, 194(4), 2001, pp. 413-419
Citations number
30
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
JOURNAL OF PATHOLOGY
ISSN journal
00223417 → ACNP
Volume
194
Issue
4
Year of publication
2001
Pages
413 - 419
Database
ISI
SICI code
0022-3417(200108)194:4<413:EOAAEG>2.0.ZU;2-W
Abstract
Amphiregulin (AR) and its receptor, epidermal growth factor receptor (EGFR) , were e-valuated by dual immunostaining in a series of 84 invasive ductal breast carcinoma specimens, 33 of which were from locally advanced inflamma tory (T4d) cancer. Co-expression of AR and EGFR was always found in non-mal ignant breast tissues adjacent to tumours (24/24). Alternatively, expressio n of AR and EGFR was found in invasive epithelial tumour cells in 50%. and 17.8% of specimens, respectively. In tumour stroma, 59.5%, and 30.9%. of sp ecimens, respectively, were positively stained. By univariate analysis, AR and EGFR expression in invasive carcinomas was correlated with large tumour size, inflammatory carcinoma, node involvement, Bloom-Richardson (SBR) gra de III, and absence of oestrogen receptor. EGFR expression in stromal cells was correlated with non-inflammatory carcinoma. A putative autocrine loop with AR and EGFR expression in invasive carcinoma was detected in 14.3%,, o f cases. Stromal expression of AR and EGFR expression in invasive tumour ce lls was detected in 11.9% of cases and related to poor prognostic parameter s. By multivariate analysis, AR expression in invasive tumour was strongly related to inflammatory carcinoma (p = 0.005) and marginally related to SBR grade III (p = 0.07). EGFR expression in invasive tumour and stromal cells was correlated with absence of oestrogen receptor and non-inflammatory car cinoma (p = 0.002 and p = 0.015, respectively). Copyright (C) 2001 John Wil ey & Sons, Ltd.