Prognostic value of protein tyrosine kinase 6 (PTK6) for long-term survival of breast cancer patients

被引:46
作者
Aubele, M. [1 ]
Walch, A. K. [1 ]
Ludyga, N. [1 ]
Braselmann, H. [2 ]
Atkinson, M. J. [3 ,4 ]
Luber, B. [5 ]
Auer, G. [6 ]
Tapio, S. [3 ]
Cooke, T. [7 ]
Bartlett, J. M. S. [8 ]
机构
[1] Helmholtz Zentrum Munchen, Inst Pathol, German Res Ctr Environm Hlth, D-85764 Neuherberg, Germany
[2] Helmholtz Ctr Munich, German Res Ctr Environm Hlth, Inst Mol Radiat Biol, D-85764 Neuherberg, Germany
[3] Helmholtz Ctr Munich, German Res Ctr Environm Hlth, Inst Radiat Biol, D-85764 Neuherberg, Germany
[4] Tech Univ Munich, Klin Strahlentherapie, D-81675 Munich, Germany
[5] Tech Univ Munich, Inst Pathol, D-81675 Munich, Germany
[6] Karolinska Hosp & Inst, Dept Pathol & Oncol, S-17176 Stockholm, Sweden
[7] Glasgow Royal Infirm, Univ Dept Surg, Glasgow G31 2ER, Lanark, Scotland
[8] Western Gen Hosp, Canc Res Ctr, Endocrine Canc Grp, Edinburgh EH4 2XR, Midlothian, Scotland
关键词
PTK6 (BRK); breast cancer; prognosis; MAPK; Sam68; PTEN;
D O I
10.1038/sj.bjc.6604660
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The cytoplasmic tyrosine kinase PTK6 (BRK) shows elevated expression in approximately two-thirds of primary breast tumours, and is implicated in EGF receptor-dependent signalling and epithelial tumorigenesis. Using immunohistochemistry, we performed a retrospective study on 426 archival breast cancer samples from patients with long-term follow-up and compared the protein expression levels of PTK6, the HER receptors, Sam68 (a substrate of PTK6), and signalling proteins including MAP kinase (MAPK), phosphorylated MAPK (P-MAPK), and PTEN. We show that PTK6 expression is of significant prognostic value in the outcome of breast carcinomas. In multivariate analysis, the disease-free survival of patients of >= 240 months was directly associated with the protein expression level of PTK6 (P <= 0.001), but was also inversely associated with nodal status (P <= 0.001) and tumour size (P <= 0.01). PTK6 expression in tumour tissue significantly correlated (P <= 0.05) with the expression of PTEN, MAPK, P-MAPK, and Sam68. To investigate whether these correlations may be due to molecular interactions between PTK6 and these proteins, we used protein extracts from the T47D cell line for immunoprecipitation and western blot analysis. By this, interactions could be demonstrated between PTK6 and MAPK, P-MAPK, HER2/neu, HER3, HER4, PTEN, and Sam68. On the basis of these results, we suggest that PTK6 may serve as a future target for the development of novel treatments in breast cancer.
引用
收藏
页码:1089 / 1095
页数:7
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