TY - JOUR
T1 - p27(Kip1) expression in breast carcinomas
T2 - An immunohistochemical study on 512 patients with long-term follow-up
AU - Barbareschi, Mattia
AU - Van Tinteren, Harm
AU - Mauri, Francesco A.
AU - Veronese, Silvio
AU - Peterse, Hans
AU - Maisonneuve, Patrik
AU - Caffo, Orazio
AU - Scaioli, Monica
AU - Doglioni, Claudio
AU - Galligioni, Enzo
AU - Dalla Palma, Paolo
AU - Michalides, Rob
PY - 2000
Y1 - 2000
N2 - p27(Kip1) (p27), a cyclin-dependent kinase inhibitor, has an important role in the progression of cells from G1 into S phase of the cell cycle. p27 may act as a tumor suppressor, and several reports suggest that loss of its expression in breast carcinoma is related to tumor progression and poor prognosis. We evaluated p27 immunohistochemical expression in 512 consecutive cases of breast carcinoma with 9 years of median-term follow-up. p27 expression was heterogeneous and frequently less intense than in normal cells. Low p27 expression (<50% of reacting cells) was associated with grade III tumors, N0 status, estrogen receptor-negative status, and low cyclin D1 expression. In the whole series of cases, p27 expression did not predict outcome. In node-negative cases (249 patients), high p27 expression indicated poor prognosis, p27 was not prognostically relevant in the group of 223 patients with pT1 disease or in the group of 154 patients <50 years of age. We also investigated the prognostic value of the combined expression of p27 and cyclin D1, but no differences in survival were seen in this bivariate analysis. (C) 2000 Wiley-Liss, Inc.
AB - p27(Kip1) (p27), a cyclin-dependent kinase inhibitor, has an important role in the progression of cells from G1 into S phase of the cell cycle. p27 may act as a tumor suppressor, and several reports suggest that loss of its expression in breast carcinoma is related to tumor progression and poor prognosis. We evaluated p27 immunohistochemical expression in 512 consecutive cases of breast carcinoma with 9 years of median-term follow-up. p27 expression was heterogeneous and frequently less intense than in normal cells. Low p27 expression (<50% of reacting cells) was associated with grade III tumors, N0 status, estrogen receptor-negative status, and low cyclin D1 expression. In the whole series of cases, p27 expression did not predict outcome. In node-negative cases (249 patients), high p27 expression indicated poor prognosis, p27 was not prognostically relevant in the group of 223 patients with pT1 disease or in the group of 154 patients <50 years of age. We also investigated the prognostic value of the combined expression of p27 and cyclin D1, but no differences in survival were seen in this bivariate analysis. (C) 2000 Wiley-Liss, Inc.
UR - http://www.scopus.com/inward/record.url?scp=0033917031&partnerID=8YFLogxK
U2 - 10.1002/1097-0215(20000520)89:3<236::AID-IJC5>3.0.CO;2-Z
DO - 10.1002/1097-0215(20000520)89:3<236::AID-IJC5>3.0.CO;2-Z
M3 - Article
C2 - 10861499
AN - SCOPUS:0033917031
SN - 0020-7136
VL - 89
SP - 236
EP - 241
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 3
ER -