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Serous and mucinous ovarian tumors express different profiles of MMP-2, -7, -9, MT1-MMP, and TIMP-1 and -2

机译:浆液性和粘液性卵巢肿瘤表达不同的MMP-2,-7,-9,MT1-MMP,TIMP-1和-2

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Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) play key roles in tumorigenesis, but little is known of their expression according to mucinous or serous type. This study aimed to evaluate the immunohistochemical expression of MMP-2, -7, -9, MT1-MMP, TIMP-1 and -2 in these tumors. A tissue microarray was set up including 99 serous (25 benign, 27 borderline, 47 malignant) and 79 mucinous (25 benign, 44 borderline, 10 malignant) ovarian tumors. Immunostaining results were scored by using the HSCORE and assessed by univariate, unsupervised hierarchical clustering and multidimensional scaling analyses. Epithelial expression of MMP-2, -7, -9, MT1-MMP, TIMP-2, but not TIMP-1, was higher in serous than mucinous tumors. Stromal expression of MMP-7 was higher in serous tumors. Alterations in MT1-MMP, MMP-7 and -9 were found in malignant serous tumors, while benign and borderline tumors shared similar expressions. By unsupervised hierarchical clustering analysis, mucinous and serous tumors were better differentiated by epithelial than stromal MMP and TIMP immunolabelling. By multidimensional scaling analysis, the expressions of MMPs and TIMPs were scattered in serous tumors and homogeneous for mucinous tumors. In conclusion, our results support the differential expression in MMPs and TIMPs of ovarian tumors according to serous or mucinous histology.
机译:基质金属蛋白酶(MMPs)及其组织抑制剂(TIMPs)在肿瘤发生中起关键作用,但根据粘液或浆液类型对其表达的了解甚少。这项研究旨在评估在这些肿瘤中MMP-2,-7,-9,MT1-MMP,TIMP-1和-2的免疫组织化学表达。建立了组织微阵列,其包括99个浆液性(25个良性,27个交界性,47个恶性)和79个粘液性(25个良性,44个交界性,10个恶性)卵巢肿瘤。使用HSCORE对免疫染色结果进行评分,并通过单变量,无监督分层聚类和多维比例分析进行评估。浆液性肿瘤中MMP-2,-7,-9,MT1-MMP,TIMP-2而不是TIMP-1的上皮表达高于粘液性肿瘤。 MMP-7的基质表达在浆液性肿瘤中较高。在恶性浆液性肿瘤中发现了MT1-MMP,MMP-7和-9的改变,而良性和交界性肿瘤的表达相似。通过无监督的分级聚类分析,上皮性粘液性和浆液性肿瘤比基质MMP和TIMP免疫标记更好地分化。通过多维标度分析,MMPs和TIMPs的表达在浆液性肿瘤中散在分布,而对于粘液性肿瘤则均匀。总之,我们的结果支持根据浆液性或粘液性组织学在卵巢肿瘤MMP和TIMPs中的差异表达。

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