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基质金属蛋白酶2的过表达预示早期非小细胞肺癌的预后不良。

Overexpression of matrix metalloproteinase 2 predicts unfavorable outcome in early-stage non-small cell lung cancer.

作者信息

Passlick B, Sienel W, Seen-Hibler R, Wöckel W, Thetter O, Mutschler W, Pantel K

机构信息

Department of Surgery, Chirurgische Klinik und Poliklinik Klinikum Innenstadt, Ludwig-Maximilians University, Munich, Germany.

出版信息

Clin Cancer Res. 2000 Oct;6(10):3944-8.

PMID:11051242
Abstract

This prospective study was performed to assess the impact of matrix metalloproteinase (MMP) 2 expression on the clinical course of patients with operable non-small cell lung cancer (NSCLC). Specimens of 193 consecutive patients with completely resected NSCLC were examined for MMP-2 expression by immunohistochemical staining with a polyclonal antibody. Homogeneous immunostaining of cancer cells was considered positive and heterogeneous, or no staining was considered negative concerning overexpression of MMP-2. Four specimens were excluded from further analyses because of unspecific staining. The median follow-up period was 71.5 months (range, 12-120 months). Overexpression of MMP-2 was observed in 64 (33.9%) of 189 patients and did not correlate with clinicopathoiogical parameters. In patients without lymph node involvement (pN0 stage) MMP-2 overexpression was an independent prognostic parameter for unfavorable outcome: Log-rank analysis showed a significant association of MMP-2 overexpression with shortened cancer-related survival (P = 0.04) and disease-free survival (P = 0.03). Multivariate regression analysis confirmed MMP-2 overexpression as predictor of shortened cancer-related survival in NSCLC without lymph node involvement (P = 0.005, relative risk, 2.6). The present study revealed that MMP-2 overexpression predicts a poor prognosis in early-stage NSCLC. Therefore, it might be worth investigating the role of MMP inhibitors as adjuvant therapeutic agents in NSCLC.

摘要

本前瞻性研究旨在评估基质金属蛋白酶(MMP)2表达对可手术切除的非小细胞肺癌(NSCLC)患者临床病程的影响。采用多克隆抗体免疫组织化学染色法,对193例连续的完全切除NSCLC患者的标本进行MMP-2表达检测。癌细胞的均匀免疫染色被视为阳性,而异质性或无染色则被视为MMP-2过表达阴性。由于非特异性染色,4份标本被排除在进一步分析之外。中位随访期为71.5个月(范围12 - 120个月)。189例患者中有64例(33.9%)观察到MMP-2过表达,且其与临床病理参数无关。在无淋巴结转移(pN0期)的患者中,MMP-2过表达是不良预后的独立预测参数:对数秩分析显示MMP-2过表达与缩短的癌症相关生存期(P = 0.04)和无病生存期(P = 0.03)显著相关。多因素回归分析证实MMP-2过表达是无淋巴结转移的NSCLC患者癌症相关生存期缩短的预测指标(P = 0.005,相对风险2.6)。本研究表明,MMP-2过表达预示早期NSCLC预后不良。因此,研究MMP抑制剂作为NSCLC辅助治疗药物的作用可能是值得的。

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