Abstract
Breast cancer is considered as one of the multifactorial diseases. The aim of the current study is to investigate the association between P-cadherin and molecular subtypes of breast cancer, especially the basal-like subtype. Two hundred and thirteen breast–invasive ductal carcinomas were involved in this study. The expressions of P-cadherin were detected via immunohistochemistry. The 213 cases were divided into luminal A, luminal B, HER2 overexpression subtype, and normal breast-like and basal-like subtypes according to the standard of molecular breast cancer subtypes. In addition, the expressions of CK5/6 and CK14 were detected to distinguish between the normal breast-like and the basal-like subtypes. P-cadherin expression was found in 91 cases of 213 breast–invasive ductal carcinomas, with a positive rate of 42.7 %. P-cadherin correlated negatively with estrogen receptor (ER) (p = 0.001) and progesterone receptor (p = 0.001), whereas it positively correlated with histologic grade (p = 0.003), NPI (p = 0.005), p53 (p = 0.038), and Ki67 (p = 0.022). P-cadherin expression showed a strong correlation with recurrence and distant metastasis (p = 0.009), and invasion of the vascular and soft tissues (p = 0.004). Moreover, P-cadherin expression existed in the basal-like and non-basal-like subtypes. During prognosis, P-cadherin expression was associated with decreased disease-free survival in patients (p = 0.009) and overall survival (OS) (p = 0.005). In addition, multivariate analysis showed that tumor grade (p = 0.021), ER (p = 0.015), clinical stage (p = 0.001), and P-cadherin (p = 0.033) were significant predictors of OS. The current data suggest that P-cadherin may be used to distinguish the basal-like subtype and to predict the outcome in view of the relationship with DFS and OS. Furthermore, P-cadherin expression may be useful in making treatment decisions.
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Liu, N., Yu, Q., Liu, T.J. et al. P-cadherin expression and basal-like subtype in breast cancers. Med Oncol 29, 2606–2612 (2012). https://doi.org/10.1007/s12032-012-0218-8
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DOI: https://doi.org/10.1007/s12032-012-0218-8