首页> 外文期刊>Respiratory medicine >Determination of the serum matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) in patients with either advanced small-cell lung cancer or non-small-cell lung cancer prior to treatment.
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Determination of the serum matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) in patients with either advanced small-cell lung cancer or non-small-cell lung cancer prior to treatment.

机译:治疗前对晚期小细胞肺癌或非小细胞肺癌患者的血清基质金属蛋白酶9(MMP-9)和基质金属蛋白酶1组织抑制剂(TIMP-1)的测定。

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This study was undertaken to examine the relationship between circulating matrix metalloproteinase (MMP-9) and tissue inhibitor of matrix metalloproteinase (TIMP-1) in our patients with either advanced small-cell lung cancer (SCLC) or non-small-cell lung cancer (NSCLC) prior to treatment. Thirty-one male and female patients with either stage III or IV NSCLC and 17 with either stage III or IV SCLC were compared to 117 age matched non-smoking controls of both sexes. Prior to any treatment of the patient, a baseline serum sample was obtained from each of the patients for the determination of circulating MMP-9 and TIMP-1 by ELISA. The results indicate that both MMP-9 and TIMP-1 are elevated in the serum of lung cancer patients when compared to the controls. This observation was true for both SCLC and NSCLC. However, the mean values for both MMP-9 and TIMP-1 in the two tumors were not different from each other. The natural physiological relationship between MMP-9 and the inhibitor TIMP-1 was lost in both SCLC and NSCLC, indicative of abnormal alterations by the tumor. The data from this study suggests that advanced lung cancer does alter the normal circulatory pattern of MMP-9 and TIMP-1. This could aid in the processes of tumor invasion and/or metastasis.
机译:这项研究旨在检查我们的晚期小细胞肺癌(SCLC)或非小细胞肺癌患者的循环基质金属蛋白酶(MMP-9)和组织金属蛋白酶组织抑制剂(TIMP-1)之间的关系(NSCLC)治疗之前。将31名患有III期或IV期NSCLC的男性和女性患者以及17名患有III期或IV期SCLC的男性患者与117名年龄匹配的非吸烟对照者进行了比较。在对患者进行任何治疗之前,从每个患者中获取基线血清样本,以通过ELISA测定循环MMP-9和TIMP-1。结果表明,与对照组相比,肺癌患者血清中的MMP-9和TIMP-1均升高。对于SCLC和NSCLC来说,这一观察都是正确的。然而,两种肿瘤中MMP-9和TIMP-1的平均值互不相同。 MLC-9和抑制剂TIMP-1之间的自然生理关系在SCLC和NSCLC中均消失,表明肿瘤异常改变。这项研究的数据表明,晚期肺癌确实会改变MMP-9和TIMP-1的正常循环模式。这可能有助于肿瘤侵袭和/或转移的过程。

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