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Erschienen in: Tumor Biology 6/2010

01.12.2010 | Research Article

Prognostic impact of ERβ and MMP7 expression on overall survival in colon cancer

verfasst von: Yu-Jing Fang, Zhen-Hai Lu, Fang Wang, Xiao-Jun Wu, Li-Ren Li, Li-Yi Zhang, Zhi-Zhong Pan, De-Sen Wan

Erschienen in: Tumor Biology | Ausgabe 6/2010

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Abstract

Estrogen receptor beta (ERβ) is the most highly expressed protein in patients with colon cancer. Matrix metalloproteinase 7 (MMP7) is consistently expressed throughout cancer progression. We have previously shown that endocrine therapy can inhibit MMP7 expression in colon cancer cells. In this study, we aim to identify the prognostic effects and correlation of ERβ and MMP7 in the context of colon cancer. ERβ and MMP7 levels were assessed by immunohistochemistry in normal mucosa and tumoral tissues from 423 patients with stage I-III colon cancer. The Cox proportional hazards regression model was applied to analyze the lifetime data, including overall survival (OS) and cause-specific survival (CSS). The 5-year survival rate was significantly higher in patients with high expression of nuclear ERβ than in patients with low expression (84.3% vs. 63.9%, respectively, p < 0.05). High expression of MMP7 was related to decreased OS (72% vs. 90%, respectively, p = 0.008) and 5-year survival (86.6% vs. 88.8%, respectively, p = 0.005) compared to patients with low expression of MMP7. In the subset of patients with high expression levels of tumoral nuclear ERβ, high expression of MMP7 was related to OS and CSS among colon cancer patients with high expression of ERβ. In conclusion, our results suggest that low expression of ERβ was a risk factor in colon cancer, and high expression of MMP7 was an independent prognostic factor of ERβ-positive patients with colon cancer.
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Metadaten
Titel
Prognostic impact of ERβ and MMP7 expression on overall survival in colon cancer
verfasst von
Yu-Jing Fang
Zhen-Hai Lu
Fang Wang
Xiao-Jun Wu
Li-Ren Li
Li-Yi Zhang
Zhi-Zhong Pan
De-Sen Wan
Publikationsdatum
01.12.2010
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 6/2010
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-010-0082-0

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