Kren L, Goncharuk V N, Krenová Z, Stratil D, Hermanová M, Skricková J, Sheehan C E, Ross J S
University Hospital Brno, Czech Republic.
Cesk Patol. 2006 Jan;42(1):16-9.
Matrix metalloproteinases (MMP's) 3, 10 and 11 (also known as stromelysins 1, 2 and 3, respectively), and matrix metalloproteinase 7 (also known as matrilysin), produced by stromal fibroblast-like cells in the vicinity of various malignancies, are suspected to have an ability to degrade components of extracellular matrix, thus promoting spread of the tumor. MMP's also have been found in epithelial tumor cells in various cancers. Tissue sections from 95 cases of non-small cell lung cancer (NSCLC) were immunostained with antibodies against MMP 3, MMP 10 and MMP 11 and sections from 99 cases of NSCLC were immunostained with an antibody against MMP 7. Cytoplasmic immunoreactivity in the tumor cells was semiquantitatively scored for intensity and distribution and correlated with tumor type, tumor grade, stage, tumor size, lymph node positivity, metastasis and survival. Overexpression of MMP 10 and MMP 11 correlated with higher grade for NSCLC (p = 0.029 and p = 0.016, respectively), and also in a subset of adenocarcinomas (AC) (p = 0.015 and p = 0.009, respectively). Also, MMP 10 and MMP 11 correlated with lymph node involvement in NSCLC (p = 0.025 and p = 0.027 respectively). No correlation was found for MMP 3. Overexpression of MMP-7 correlated with tumor stage (p = 0.0001) and was associated with adverse clinical outcome (p = 0.0001) in NSCLC and also in separate squamous cell carcinoma (SCC) (p = 0.003) and AC (p = 0.004) tumor groups.
基质金属蛋白酶(MMP)3、10和11(分别也称为基质溶解素1、2和3)以及基质金属蛋白酶7(也称为基质溶素),由各种恶性肿瘤附近的基质成纤维细胞样细胞产生,被怀疑具有降解细胞外基质成分的能力,从而促进肿瘤扩散。在各种癌症的上皮肿瘤细胞中也发现了MMP。用抗MMP 3、MMP 10和MMP 11的抗体对95例非小细胞肺癌(NSCLC)的组织切片进行免疫染色,并用抗MMP 7的抗体对99例NSCLC的组织切片进行免疫染色。对肿瘤细胞中的细胞质免疫反应性进行强度和分布的半定量评分,并与肿瘤类型、肿瘤分级、分期、肿瘤大小、淋巴结阳性、转移和生存率相关联。MMP 10和MMP 11的过表达与NSCLC的高分级相关(分别为p = 0.029和p = 0.016),在腺癌(AC)亚组中也是如此(分别为p = 0.015和p = 0.009)。此外,MMP 10和MMP 11与NSCLC中的淋巴结受累相关(分别为p = 0.025和p = 0.027)。未发现MMP 3有相关性。MMP - 7的过表达与肿瘤分期相关(p = 0.0001),并且与NSCLC以及单独的鳞状细胞癌(SCC)(p = 0.003)和AC(p = 0.004)肿瘤组的不良临床结局相关(p = 0.0001)。