Bax and Bc12 are functionally antagonistic proteins which control apoptosis, whose expression in human tumours could be of prognostic value. We evaluated Bax and Bcl2 expression in 239 breast carcinomas (99 N0, 140 N1/2) with long term follow-up (median 79 months, range 11-140) in relation to clinic
ErbB-receptors expression and survival in breast carcinoma: A 15-year follow-up study
✍ Scribed by Simonetta Bianchi; Domenico Palli; Mario Falchetti; Calogero Saieva; Giovanna Masala; Biancamaria Mancini; Ramona Lupi; Cristiana Noviello; Jasminka Omerovic; Milena Paglierani; Vania Vezzosi; Maurizio Alimandi; Renato Mariani-Costantini; Laura Ottini
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 101 KB
- Volume
- 206
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Aberrant expression of the epidermal growth factor receptor family has been implicated in the pathogenesis and progression of breast cancer and associated with poor prognosis. To evaluate the prognostic impact of the ErbB receptors expression profile, we analyzed a well‐characterized series of 145 primary breast carcinomas for the simultaneous expression of epidermal growth factor receptor (EGFR/HER‐1), ErbB‐2 (HER‐2), ErbB‐3 (HER‐3), and ErbB‐4 (HER‐4), using immunohistochemistry. Tumors were considered negative or positive for each marker when less than or more than 25% of the cancer cells were immunopositive. Expression of EGFR, ErbB‐2, ErbB‐3, and ErbB‐4 was observed in 31 (21.4%), 65 (44.8%), 72 (49.7%), and 81 (55.9%) of the cases, respectively. There were significant associations between EGFR expression and pT status (P = 0.01), and between ErbB‐3 expression and pN (P = 0.003), menopausal (P = 0.01) and PR (P < 0.001) status. The majority of the cases co‐expressed two or more receptors. ErbB‐3 resulted positive in 51/81 (63.0%) of the ErbB‐4 positive cases and ErbB‐3/ErbB‐4 co‐expression was statistically significant (P = 0.0003). As expected, ErbB‐2 expression was associated with reduced overall survival at 15 years of follow‐up (P = 0.04), even after adjusting for a series of other prognostic factors (P = 0.05). Moreover, cumulative analysis of ErbB‐2/3/4 expression showed a strong positive association between higher total ErbB‐2/3/4 expression score and worse prognosis (P = 0.002). The simultaneous expression in cancer cells of more than one ErbB receptor identifies a subset of breast cancer patients at high risk for poor survival. J.Cell.Physiol. © 2005 Wiley‐Liss, Inc.
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