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Association of cyclooxygenase-2 and matrix metalloproteinase-2 expression in human breast cancer

机译:乳腺癌中环氧合酶2和基质金属蛋白酶2表达的关联

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摘要

Expression of cyclooxygenase-2 (COX-2) and matrix metalloproteinase-2 (MMP-2) associates with reduced survival in human breast cancer. COX-2 may be directly involved with mammary carcinogenesis, since expression of COX-2 is sufficient for formation of breast tumors in transgenic mice, and COX-2 selective inhibitors can suppress tumorigenesis in rodent models of breast cancer. MMP-2 is an extracellular matrix degrading proteolytic enzyme that bas been linked to invasion and metastasis. A direct link between COX-2 and MMP-2 may exist, since inhibition of COX-2 activity can result in reduction of MMP-2 expression and activity. In this study we analyzed protein expression of COX-2 and MMP-2 in tissue array specimens of 278 invasive breast cancers by immunohistochemistry. Immunopositivity of these two markers was correlated with each other and with various clinicopathological parameters including survival. We found high COX-2 expression in 30% and high MMP-2 expression in 83% of the breast cancer specimens, and there was a positive association between the expression of these two factors (p=0.003). It was especially evident that whenever COX-2 expression was high, MMP-2 expression was almost invariably high (95%). Furthermore, high expression of either COX-2 or MMP-2 associated with decreased disease specific survival when compared with the COX-2 or MPP-2 low group (p=0.026 and p=0.021, respectively). Taken together, our results indicate that expression of COX-2 protein is associated with expression of MMP-2 protein in human breast cancer and that both COX-2 and MMP-2 are markers of poor prognosis in breast cancer.
机译:环氧合酶2(COX-2)和基质金属蛋白酶2(MMP-2)的表达与人类乳腺癌的生存期缩短有关。由于COX-2的表达足以在转基因小鼠中形成乳腺肿瘤,而COX-2选择性抑制剂可以抑制乳腺癌啮齿动物模型中的肿瘤发生,因此COX-2可能直接与乳腺癌变有关。 MMP-2是一种细胞外基质降解蛋白水解酶,与入侵和转移有关。 COX-2和MMP-2之间可能存在直接联系,因为抑制COX-2活性可能导致MMP-2表达和活性降低。在这项研究中,我们通过免疫组织化学分析了278例浸润性乳腺癌的组织样本中COX-2和MMP-2的蛋白表达。这两种标记物的免疫阳性相互之间以及与包括生存在内的各种临床病理学参数相关。我们发现30%的乳腺癌标本中COX-2高表达,而83%的乳腺癌标本中MMP-2高表达,这两个因子的表达呈正相关(p = 0.003)。特别明显的是,每当COX-2表达高时,MMP-2表达几乎总是高(95%)。此外,与低COX-2或MPP-2低组相比,COX-2或MMP-2的高表达与疾病特异性生存率降低相关(分别为p = 0.026和p = 0.021)。两者合计,我们的结果表明,COX-2蛋白的表达与人乳腺癌中MMP-2蛋白的表达有关,并且COX-2和MMP-2都是乳腺癌预后不良的标志。

著录项

  • 来源
    《Breast Cancer Research and Treatment》 |2005年第3期|215-220|共6页
  • 作者单位

    Department of Pathology Helsinki University Central HospitalMolecular and Cancer Biology Research Program Biomedicum Helsinki University of Helsinki;

    Department of Oncology and Radiotherapy University of Oulu and Oulu University Hospital;

    Department of Oncology Helsinki University Central Hospital;

    Molecular and Cancer Biology Research Program Biomedicum Helsinki University of HelsinkiDepartment of Oncology Helsinki University Central Hospital;

    Department of Pathology Helsinki University Central HospitalDepartment of Surgery Helsinki University Central Hospital;

    Department of Pathology Helsinki University Central HospitalMolecular and Cancer Biology Research Program Biomedicum Helsinki University of Helsinki;

    Department of Oncology and Radiotherapy University of Oulu and Oulu University Hospital;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    breast cancer; cyclooxygenase-2; matrix metalloproteinase-2; prognosis; survival;

    机译:乳腺癌;环氧合酶-2;基质金属蛋白酶-2;预后;生存期;

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