@article {7618,
	title = {High MET expression is an adverse prognostic factor in patients with triple-negative breast cancer},
	journal = {British Journal of Cancer},
	volume = {108},
	year = {2013},
	note = {Cited By :26Export Date: 21 February 2017},
	month = {2013},
	pages = {1100 - 1105},
	abstract = {Background: The mesenchymal-epithelial transition (MET) pathway is frequently altered in tumours. The purpose of our study was to determine the prognostic value of tumour MET expression levels in patients with triple-negative breast cancer (TNBC), in order to strengthen the rationale for targeted therapy of TNBC using MET inhibitors. Methods: We determined expression of MET in formalin-fixed paraffin-embedded surgical specimens of TNBC by immunohistochemistry. Recurrence-free and overall survival was analysed with Cox models adjusted for clinical and pathological factors.Results:Immunostaining for MET was classified as high in 89 of 170 (52\%) tumours. MET expression was more frequently observed in G3 carcinomas (P=0.02) but was not significantly associated to any of the other clinical or pathological parameters. High MET expression predicted shorter survival of the patients. Multivariate Cox proportional hazards regression analyses identified MET to be an independent prognostic factor for recurrence (adjusted hazard ratio (HR) for recurrence 3.43; 95\% confidence interval (CI) 1.65-7.12; P=0.001) and death (adjusted HR for death 3.74; 95\% CI 1.65-8.46; P=0.002). Conclusion: These results provide further evidence that the MET pathway could be exploited as a target for TNBC. {\textcopyright} 2013 Cancer Research UK. All rights reserved.},
	keywords = {Biomarkers, MET, Prognosis, triple-negative breast cancer},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84875418041\&doi=10.1038\%2fbjc.2013.31\&partnerID=40\&md5=2477ac92678526c58988ffbb7c349f66},
	author = {Zagouri, F. and Bago-Horvath, Z. and R{\"o}ssler, F. and Brandstetter, A. and Bartsch, R. and Papadimitriou, C.A. and Dimitrakakis, C. and Tsigginou, A. and Papaspyrou, I. and Giannos, A. and Dimopoulos, M.-A. and Filipits, M.}
}
