P-cadherin expression as a prognostic biomarker in a 3992 case tissue microarray series of breast cancer

被引:52
作者
Turashvili, Gulisa
McKinney, Steven E.
Goktepe, Ozge
Leung, Samuel C. [2 ]
Huntsman, David G. [2 ]
Gelmon, Karen A. [3 ]
Los, Gerrit [4 ]
Rejto, Paul A. [4 ]
Aparicio, Samuel A. J. R. [1 ]
机构
[1] UBC BC Canc Agcy, Nan & Lorraine Robertson Chair, Dept Mol Oncol, BC Canc Res Ctr, Vancouver, BC V5Z 1L3, Canada
[2] Univ British Columbia, Genet Pathol Evaluat Ctr, Vancouver, BC V5Z 1M9, Canada
[3] BC Canc Agcy, Vancouver, BC, Canada
[4] Pfizer Worldwide Res & Dev, Oncol Res Unit, San Diego, CA USA
关键词
breast cancer; immunohistochemistry; P-cadherin; prognosis; tissue microarray; BASAL EPITHELIAL PHENOTYPE; GROWTH-FACTOR RECEPTOR; PLACENTAL CADHERIN; ESTROGEN-RECEPTOR; DUCTAL CARCINOMA; MAMMARY-GLAND; BRCA1; STATUS; N-CADHERIN; IN-SITU; MARKERS;
D O I
10.1038/modpathol.2010.189
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
P-cadherin is a calcium-dependent cell-cell adhesion glycoprotein. P-cadherin expression is restricted to the myoepithelial cells in normal breast tissue, and aberrant staining has also been described in invasive tumors. Several small studies have reported P-cadherin as a marker of poor outcome in breast cancer patients but its prognostic significance in relation to other variables has not been established in a large series of breast cancers. A tissue microarray was constructed from 3992 cases of invasive breast carcinoma, and P-cadherin expression was evaluated using immunohistochemistry. Median follow-up was 12.5 years. The immuno-histochemistry-based definitions of cancer subtypes were luminal (ER+ or PR+/HER2-), luminal/HER2+ (ER+ or PR+/HER2+), HER2+ (ER-/PR-/HER2+), and basal (ER-/PR-/HER2-/CK5/6+ or EGFR+). Clinical covariate and biomarker associations were assessed using contingency tables, and Pearson's chi(2) or Fisher's exact test. Survival associations were assessed using Kaplan-Meier plots, logrank and Breslow tests, and Cox proportional hazards regression analysis. P-cadherin was expressed in 34.8% (1290/3710, 50% cut point) of cases. P-cadherin staining was strongly associated with HER2+ and basal carcinoma subtypes (P<0.0005). P-cadherin-positive patients showed significantly poorer short-term (0-10 years) overall survival, disease-specific survival, distant relapse-free interval, and locoregional relapse-free interval in univariable models (P<0.05). In multivariable Cox models containing standard clinical covariates and cancer subtypes, P-cadherin did not show independent prognostic value. P-cadherin expression was positively associated with histological grade, chemotherapy, Ki-67, EGFR, CK5/6, p53, YB-1, and HER2 expression (P<0.002), and negatively associated with age at diagnosis, ER, PR, and Bcl-2 expression (P<0.0005). This study shows the value of P-cadherin as a marker of poor prognosis. The large sample size of this series clarifies contradictory findings of many smaller studies. P-cadherin positivity is associated with high-grade tumor subtypes and well-established markers of poor prognosis, and may represent a promising antibody therapeutic target. Modern Pathology (2011) 24, 64-81; doi:10.1038/modpathol.2010.189; published online 17 September 2010
引用
收藏
页码:64 / 81
页数:18
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