Clinical Implications of T[beta]RII Expression in Breast Cancer

To explore the relationship between T[beta]RII [type II TGF[beta] (transforming growth factor [beta]) receptor] expression and clinicopathological characteristics, and to evaluate the prognostic significance of T[beta]RII expression in breast cancer. Clinicopathological data and prognostic informati...

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Veröffentlicht in:PloS one 2015-11, Vol.10 (11)
Hauptverfasser: Gao, Ningning, Zhai, Qixi, Li, Yinyan, Huang, Kun, Bian, Donglin, Wang, Xuemei, Liu, Caigang, Xu, Hong, Zhang, Teng
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container_title PloS one
container_volume 10
creator Gao, Ningning
Zhai, Qixi
Li, Yinyan
Huang, Kun
Bian, Donglin
Wang, Xuemei
Liu, Caigang
Xu, Hong
Zhang, Teng
description To explore the relationship between T[beta]RII [type II TGF[beta] (transforming growth factor [beta]) receptor] expression and clinicopathological characteristics, and to evaluate the prognostic significance of T[beta]RII expression in breast cancer. Clinicopathological data and prognostic information of 108 patients with histologically confirmed breast cancer who were surgically treated at China Medical University between January 2007 and September 2008 were reviewed and the association between the clinicopathological characteristics and T[beta]RII expression was analyzed by chi-square test and multivariate analysis. The expression of T[beta]RII was assessed by immunohistochemistry. Of the 108 patients, 60 cases were T[beta]RII positive and 48 cases were negative. There was no significant association between T[beta]RII expression of the patients older than 40 years and that of the younger than 40 years (56.0% vs 50.0%; P = 0.742). The T[beta]RII expression rate was significantly increased in patients with lymph node metastasis compared to those without lymph node metastasis (67.40% vs 46.8%; P = 0.033). Statistically significant relationships were found between increasing tumor clinical stage and high T[beta]RII expression (P = 0.011). T[beta]RII expression was not associated with the expression of ER(estrogen receptor), PR, (progesterone receptor), Her-2 (human epidermal growth factor receptor 2) (P = 0.925,P = 0.861, and P = 0.840, respectively). Patients with high T[beta]RII expression showed poorer 5-year disease-free survival (DFS) compared to those with low expression (66.7% vs 45.6%; P = 0.028) by univariate analysis. Survival analysis demonstrated that T[beta]RII was associated with poor DFS (P = 0.011). Subgroup analysis revealed that T[beta]RII expression was associated with shorter DFS in patients with lymph node metastasis, ER-positive, PR-positive or Her-2-negative tumors (P = 0.006, P = 0.016, P = 0.022, and P = 0.033, respectively). Cox regression analysis revealed that high T[beta]RII expression was related to poor 5-year DFS, and it was an independent factor for predicting the poor outcome for breast cancer patients (P = 0.016). High levels of T[beta]RII expression were associated with lymph node metastasis, increasing tumor clinical stage, and poorer 5-year DFS in patients with breast cancer. T[beta]RII may be a potential prognostic marker for breast cancer.
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Clinicopathological data and prognostic information of 108 patients with histologically confirmed breast cancer who were surgically treated at China Medical University between January 2007 and September 2008 were reviewed and the association between the clinicopathological characteristics and T[beta]RII expression was analyzed by chi-square test and multivariate analysis. The expression of T[beta]RII was assessed by immunohistochemistry. Of the 108 patients, 60 cases were T[beta]RII positive and 48 cases were negative. There was no significant association between T[beta]RII expression of the patients older than 40 years and that of the younger than 40 years (56.0% vs 50.0%; P = 0.742). The T[beta]RII expression rate was significantly increased in patients with lymph node metastasis compared to those without lymph node metastasis (67.40% vs 46.8%; P = 0.033). Statistically significant relationships were found between increasing tumor clinical stage and high T[beta]RII expression (P = 0.011). T[beta]RII expression was not associated with the expression of ER(estrogen receptor), PR, (progesterone receptor), Her-2 (human epidermal growth factor receptor 2) (P = 0.925,P = 0.861, and P = 0.840, respectively). Patients with high T[beta]RII expression showed poorer 5-year disease-free survival (DFS) compared to those with low expression (66.7% vs 45.6%; P = 0.028) by univariate analysis. Survival analysis demonstrated that T[beta]RII was associated with poor DFS (P = 0.011). Subgroup analysis revealed that T[beta]RII expression was associated with shorter DFS in patients with lymph node metastasis, ER-positive, PR-positive or Her-2-negative tumors (P = 0.006, P = 0.016, P = 0.022, and P = 0.033, respectively). Cox regression analysis revealed that high T[beta]RII expression was related to poor 5-year DFS, and it was an independent factor for predicting the poor outcome for breast cancer patients (P = 0.016). High levels of T[beta]RII expression were associated with lymph node metastasis, increasing tumor clinical stage, and poorer 5-year DFS in patients with breast cancer. 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Clinicopathological data and prognostic information of 108 patients with histologically confirmed breast cancer who were surgically treated at China Medical University between January 2007 and September 2008 were reviewed and the association between the clinicopathological characteristics and T[beta]RII expression was analyzed by chi-square test and multivariate analysis. The expression of T[beta]RII was assessed by immunohistochemistry. Of the 108 patients, 60 cases were T[beta]RII positive and 48 cases were negative. There was no significant association between T[beta]RII expression of the patients older than 40 years and that of the younger than 40 years (56.0% vs 50.0%; P = 0.742). The T[beta]RII expression rate was significantly increased in patients with lymph node metastasis compared to those without lymph node metastasis (67.40% vs 46.8%; P = 0.033). Statistically significant relationships were found between increasing tumor clinical stage and high T[beta]RII expression (P = 0.011). T[beta]RII expression was not associated with the expression of ER(estrogen receptor), PR, (progesterone receptor), Her-2 (human epidermal growth factor receptor 2) (P = 0.925,P = 0.861, and P = 0.840, respectively). Patients with high T[beta]RII expression showed poorer 5-year disease-free survival (DFS) compared to those with low expression (66.7% vs 45.6%; P = 0.028) by univariate analysis. Survival analysis demonstrated that T[beta]RII was associated with poor DFS (P = 0.011). Subgroup analysis revealed that T[beta]RII expression was associated with shorter DFS in patients with lymph node metastasis, ER-positive, PR-positive or Her-2-negative tumors (P = 0.006, P = 0.016, P = 0.022, and P = 0.033, respectively). Cox regression analysis revealed that high T[beta]RII expression was related to poor 5-year DFS, and it was an independent factor for predicting the poor outcome for breast cancer patients (P = 0.016). High levels of T[beta]RII expression were associated with lymph node metastasis, increasing tumor clinical stage, and poorer 5-year DFS in patients with breast cancer. 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Clinicopathological data and prognostic information of 108 patients with histologically confirmed breast cancer who were surgically treated at China Medical University between January 2007 and September 2008 were reviewed and the association between the clinicopathological characteristics and T[beta]RII expression was analyzed by chi-square test and multivariate analysis. The expression of T[beta]RII was assessed by immunohistochemistry. Of the 108 patients, 60 cases were T[beta]RII positive and 48 cases were negative. There was no significant association between T[beta]RII expression of the patients older than 40 years and that of the younger than 40 years (56.0% vs 50.0%; P = 0.742). The T[beta]RII expression rate was significantly increased in patients with lymph node metastasis compared to those without lymph node metastasis (67.40% vs 46.8%; P = 0.033). Statistically significant relationships were found between increasing tumor clinical stage and high T[beta]RII expression (P = 0.011). T[beta]RII expression was not associated with the expression of ER(estrogen receptor), PR, (progesterone receptor), Her-2 (human epidermal growth factor receptor 2) (P = 0.925,P = 0.861, and P = 0.840, respectively). Patients with high T[beta]RII expression showed poorer 5-year disease-free survival (DFS) compared to those with low expression (66.7% vs 45.6%; P = 0.028) by univariate analysis. Survival analysis demonstrated that T[beta]RII was associated with poor DFS (P = 0.011). Subgroup analysis revealed that T[beta]RII expression was associated with shorter DFS in patients with lymph node metastasis, ER-positive, PR-positive or Her-2-negative tumors (P = 0.006, P = 0.016, P = 0.022, and P = 0.033, respectively). Cox regression analysis revealed that high T[beta]RII expression was related to poor 5-year DFS, and it was an independent factor for predicting the poor outcome for breast cancer patients (P = 0.016). High levels of T[beta]RII expression were associated with lymph node metastasis, increasing tumor clinical stage, and poorer 5-year DFS in patients with breast cancer. T[beta]RII may be a potential prognostic marker for breast cancer.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0141412</doi></addata></record>
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subjects Breast cancer
Gene expression
Genetic aspects
Health aspects
Prognosis
Properties
Transforming growth factors
title Clinical Implications of T[beta]RII Expression in Breast Cancer
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