Matrix metalloproteinase-13 expression is associated with bone marrow microinvolvement and prognosis in non-small cell lung cancer

被引:69
作者
Hsu, Chung-Ping
Shen, Gwan-Han
Ko, Jiunn-Liang
机构
[1] Taichung Vet Gen Hosp, Dept Surg, Div Thorac Surg, Taichung, Taiwan
[2] Taichung Vet Gen Hosp, Dept Med, Div Chest Med, Taichung, Taiwan
[3] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
[4] Chung Shang Med Univ, Inst Med & Mol Toxicol, Taichung, Taiwan
关键词
matrix metalloproteinase; bone marrow microinvolvement; non-small cell lung cancer;
D O I
10.1016/j.lungcan.2006.01.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our previous study demonstrated that bone marrow microinvolvement (BMM) is an epiphenomenon of tumor progression rather than a prognostic factor in non-small cell lung cancer. We hypothesize that an increase in mesenchymal. transition power in epithetial tumor cells by up-regulation of the matrix metalloproteinases (MMPs) may contribute to the existence of BMM and poorer prognosis. Hereby we conducted a prospective study of BMM and MMPs expression in a cohort of 57 non-small cell lung cancer patients. Bone aspirates were examined by immunohistochemical stains. Expressions of MMPs were checked by Human MMP primer set kit (Maxim Biotech, USA). Correlations between the MMPs expression and BMM, nodal metastasis, and prognosis were examined. Cox model analysis was used to identify independent prognostic factors. Though positive BMM was identified in 38 (66.7%) of the patients, none of the clinicopathological factors, including sex, age, cell types, tumor differentiation, nodal metastasis and TNM status of the tumor, was related to BMM by the tumor cells. Up-regulation was observed in a broad spectrum of MMPs with the exception of MMP-3. However, only MMP-13 expression correlated with the existence of BMM (p=0.006). Univariate analysis revealed MMP-3, MMP-7 and MMP-13 as negative prognostic factors. Cox model analysis revealed T-status, cell differentiation, and MMP-13 expression of the tumor as independent prognostic factors. The overall 5-year survival rate of the patients was 36.8%. The existence of BMM itself did not influence the prognosis (p = 0.109), however, patients with positive MMP-13 expression (N = 34) had a poorer 5-year survival rate of 26.5% (p = 0.025). In summary, non-small cell lung cancer cells with MMP-13 expression, despite of BMM status, tend to shed and aggregate in the bone marrow, which is subsequently reflected in a poorer survival rate. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:349 / 357
页数:9
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