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Published in: Journal of Cancer Research and Clinical Oncology 11/2013

01-11-2013 | Original Paper

RUNX3 is a prognostic marker and potential therapeutic target in human breast cancer

Authors: Jin Bai, Hong-Mei Yong, Fei-Fei Chen, Wen-Bo Song, Chen Li, Hui Liu, Jun-Nian Zheng

Published in: Journal of Cancer Research and Clinical Oncology | Issue 11/2013

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Abstract

Purpose

To evaluate the role of RUNX3 in breast cancer pathogenesis, we examined the RUNX3 expression in breast cancer tissues and analyzed the correlation between RUNX3 expression and clinicopathologic variables and patients survival.

Methods

We evaluated the RUNX3 expression by immunohistochemistry using a tissue microarray containing 256 specimens of breast cancer patients. We also studied the role of RUNX3 in cell migration and invasion by performing cell migration and invasion assay. Differential expression of metastasis-related genes after RUNX3 restoration was analyzed using the Human Tumor Metastasis PCR Array.

Results

The RUNX3 expression was significantly correlated with breast cancer histology grade (P = 0.000), and low RUNX3 expression strongly correlated with worse 5-year overall and disease-specific survival rates (P = 0.000 and P = 0.001, respectively). Furthermore, we found that RUNX3 restoration suppressed breast cancer metastasis by controlling cell migration and invasion capacity. Finally, gene expression profiles of RUNX3-549 and Ctrl-549 cells showed matrix metalloproteinase-2 (MMP-2) was the most significant gene among the 84 metastasis-related genes influenced by RUNX3 reintroduction.

Conclusions

Reduced RUNX3 expression is significantly correlated with breast cancer progression and predicts worse survival. RUNX3 regulates breast cancer cell migration and invasion through the MMP-2 pathway.
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Metadata
Title
RUNX3 is a prognostic marker and potential therapeutic target in human breast cancer
Authors
Jin Bai
Hong-Mei Yong
Fei-Fei Chen
Wen-Bo Song
Chen Li
Hui Liu
Jun-Nian Zheng
Publication date
01-11-2013
Publisher
Springer Berlin Heidelberg
Published in
Journal of Cancer Research and Clinical Oncology / Issue 11/2013
Print ISSN: 0171-5216
Electronic ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-013-1498-x

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