Wu Chun-Ying, Wu Ming-Shiang, Chiang En-Pei, Chen Yi-Ju, Chen Chien-Jen, Chi Nai-Hui, Shih Ying-Ting, Chen Gran-Hum, Lin Jaw-Town
Graduate Institute of Clinical Medicine, College of Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Clin Cancer Res. 2007 Apr 1;13(7):2054-60. doi: 10.1158/1078-0432.CCR-06-2299.
Matrix metalloproteinase-9 (MMP-9) in blood is a promising new tumor marker. The aims of the present study are to compare the usefulness of plasma and serum MMP-9 levels for predicting gastric cancer development, invasion, and survival.
In this nested case-control study, 114 gastric cancer patients and 87 healthy controls were enrolled. MMP-9 levels and activities were quantitatively measured by ELISA assay and zymography. The results were compared with the occurrence, clinicopathologic features, and outcomes of gastric cancer patients. The follow-up time for all patients was at least 5 years.
Serum MMP-9 levels were significantly higher than plasma MMP-9 levels. Both plasma and serum MMP-9 levels correlated significantly with active MMP-9 identified by zymography (P = 0.002 and P = 0.048, respectively). Plasma MMP-9 level was significantly elevated in gastric cancer patients when compared with control subjects (P < 0.001). Serum MMP-9 levels did not differ between the groups. Receiver-operator characteristics analysis showed the values of sensitivity (82.5%) and specificity (65.5%) at the maximum accuracy for plasma MMP-9 at >or=60 ng/mL (P < 0.001). Elevated plasma MMP-9 correlated significantly with lymph node metastasis [odds ratio (OR), 3.43; P = 0.019], lymphatic invasion (OR, 7.58; P = 0.009), and venous invasion (OR, 4.14; P = 0.033). Patients with elevated plasma MMP-9 levels had poorer survival rates than those with normal plasma MMP-9 levels (P = 0.038). Serum MMP-9 level did not correlate well with gastric cancer-invasive phenotypes or survival.
Our results suggest plasma MMP-9 level is a better marker than serum MMP-9 level for predicting gastric cancer development and progression.
血液中的基质金属蛋白酶-9(MMP-9)是一种很有前景的新型肿瘤标志物。本研究的目的是比较血浆和血清MMP-9水平在预测胃癌发生、侵袭及生存方面的效用。
在这项巢式病例对照研究中,纳入了114例胃癌患者和87例健康对照者。采用酶联免疫吸附测定(ELISA)法和酶谱分析法对MMP-9水平及活性进行定量测定。将结果与胃癌患者的发病情况、临床病理特征及预后进行比较。所有患者的随访时间至少为5年。
血清MMP-9水平显著高于血浆MMP-9水平。血浆和血清MMP-9水平均与酶谱分析法鉴定的活性MMP-9显著相关(分别为P = 0.002和P = 0.048)。与对照受试者相比,胃癌患者的血浆MMP-9水平显著升高(P < 0.001)。两组间血清MMP-9水平无差异。受试者工作特征分析显示,血浆MMP-9≥60 ng/mL时,在最大准确度下的灵敏度值为82.5%,特异度值为65.5%(P < 0.001)。血浆MMP-9升高与淋巴结转移[比值比(OR),3.43;P = 0.019]、淋巴管侵袭(OR,7.58;P = 0.009)及静脉侵袭(OR,4.14;P = 0.033)显著相关。血浆MMP-9水平升高的患者生存率低于血浆MMP-9水平正常的患者(P = 0.038)。血清MMP-9水平与胃癌侵袭性表型或生存率的相关性不佳。
我们的结果表明,对于预测胃癌的发生和进展而言,血浆MMP-9水平是比血清MMP-9水平更好的标志物。