首页> 外文期刊>Japanese journal of clinical oncology. >Association between cyclooxygenase-2 and matrix metalloproteinase-2 expression in non-small cell lung cancer.
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Association between cyclooxygenase-2 and matrix metalloproteinase-2 expression in non-small cell lung cancer.

机译:非小细胞肺癌中环氧合酶2和基质金属蛋白酶2表达之间的关联。

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摘要

BACKGROUND: Cyclooxygenase-2 (COX-2) contributes to invasiveness of cancer through activation of several matrix metalloproteinases (MMPs). Matrix metalloproteinase-2 (MMP-2) is a proteolytic enzyme that degrades the extracellular matrix, and has been linked to invasion and metastasis. This study aims to assess the correlation of the COX-2 expression and the MMP-2 expression in patients with non-small cell lung cancer (NSCLC). METHODS: We analyzed the protein expressions of COX-2 and MMP-2 by immunohistochemical staining on the tissue array specimens from 204 patients with completely resected NSCLC. A <10% immunostaining of the cancer cells was considered negative, while >10% was considered positive. RESULTS: The COX-2 expression was positive in 68.1% and that of the MMP-2 was positive in 45.6%. The positive expression rate of MMP-2 (52.5%) in the positive COX-2 group was higher than that in the negative COX-2 group (30.8%, P = 0.004). Furthermore, the MMP-2 expression was associated with lymph node involvement, the tumor stage and the histological type. The patients with a positive MMP-2 expression showed a reduced survival (P = 0.048). CONCLUSIONS: The COX-2 expression is associated with the MMP-2 expression in NSCLC patients: the latter may also be associated with tumor progression and reduced survival in NSCLC patients.
机译:背景:环氧合酶2(COX-2)通过激活几种基质金属蛋白酶(MMP)促进癌症的侵袭。基质金属蛋白酶2(MMP-2)是一种蛋白水解酶,可降解细胞外基质,并与侵袭和转移有关。这项研究旨在评估非小细胞肺癌(NSCLC)患者中COX-2表达和MMP-2表达的相关性。方法:采用免疫组织化学方法对204例完全切除的NSCLC患者的组织样本进行免疫组织化学染色,分析COX-2和MMP-2的蛋白表达。癌细胞的<10%免疫染色被认为是阴性的,而> 10%被认为是阳性的。结果:COX-2表达阳性率为68.1%,MMP-2表达阳性率为45.6%。阳性COX-2组中MMP-2的阳性表达率(52.5%)高于阴性COX-2组(30.8%,P = 0.004)。此外,MMP-2表达与淋巴结受累,肿瘤分期和组织学类型有关。 MMP-2表达阳性的患者生存率降低(P = 0.048)。结论:NSCLC患者的COX-2表达与MMP-2表达有关;后者也可能与NSCLC患者的肿瘤进展和生存期降低有关。

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