| BMC Cancer | |
| Co-expression of parathyroid hormone related protein and TGF-beta in breast cancer predicts poor survival outcome | |
| Research Article | |
| Rongrong Cui1  Xiaoyan Lin1  Zhengyuan Wang1  Cheng Xu1  Hongwei Zhang2  Hongyu He3  Yuan Sheng4  | |
| [1] Department of Breast Surgery, Yangpu Hospital, Tongji University School of Medicine, 200090, Shanghai, China;Department of General Surgery, Zhongshan Hospital, Fudan University, 200032, Shanghai, China;Department of Intensive Care Medicine, Zhongshan Hospital, Fudan University, 200032, Shanghai, China;Department of Thyroid and Breast Surgery, Changhai Hospital, 200433, Shanghai, China; | |
| 关键词: Breast cancer; TGF-β; PTHrP; Prognosis; Survival analysis; | |
| DOI : 10.1186/s12885-015-1873-x | |
| received in 2015-05-20, accepted in 2015-10-30, 发布年份 2015 | |
| 来源: Springer | |
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【 摘 要 】
BackgroundBetter methods to predict prognosis can play a supplementary role in administering individualized treatment for breast cancer patients. Altered expressions of PTHrP and TGF-β have been observed in various types of human cancers. The objective of the current study was to evaluate the association of PTHrP and TGF-β level with the clinicopathological features of the breast cancer patients.MethodsImmunohistochemistry was used to examine PTHrP and TGF-β protein expression in 497 cases of early breast cancer, and Kaplan-Meier method and COX’s Proportional Hazard Model were applied to the prognostic value of PTHrP and TGF-β expression.ResultsBoth over-expressed TGF-β and PTHrP were correlated with the tumor in larger size, higher proportion of axillary lymph node metastasis and later clinical stage. Additionally, the tumors with a high TGF-β level developed poor differentiation, and only TGF-β expression was associated with disease-free survival (DFS) of the breast cancer patients. Followed up for a median of 48 months, it was found that only the patients with negative TGF-β expression had longer DFS (P < 0.05, log-rank test). Nevertheless, those with higher PTHrP expression tended to show a higher rate of bone metastasis (67.6 % vs. 45.8 %, P = 0.019). In ER negative subgroup, those who developed PTHrP positive expression presented poor prognosis (P < 0.05, log-rank test). The patients with both positive TGF-β and PTHrP expression were significantly associated with the high risk of metastases. As indicated by Cox’s regression analysis, TGF-β expression and the high proportion of axillary lymph node metastasis served as significant independent predictors for breast cancer recurrence.ConclusionsTGF-β and PTHrP were confirmed to be involved in regulating the malignant progression in breast cancer, and PTHrP expression, to be associated with bone metastasis as a potential prognostic marker in ER negative breast cancer.
【 授权许可】
CC BY
© Xu et al. 2015
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202311105593225ZK.pdf | 974KB |
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