首页> 美国卫生研究院文献>British Journal of Cancer >Cathepsin-D urokinase plasminogen activator and type-1 plasminogen activator inhibitor in early breast cancer: an immunohistochemical study of prognostic value and relations to tenascin-C and other factors
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Cathepsin-D urokinase plasminogen activator and type-1 plasminogen activator inhibitor in early breast cancer: an immunohistochemical study of prognostic value and relations to tenascin-C and other factors

机译:组织蛋白酶D尿激酶纤溶酶原激活物和1型纤溶酶原激活物抑制剂在早期乳腺癌中的免疫组化研究:预后价值及其与腱生蛋白C和其他因素的关系

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摘要

Cytosolic determinations of cathepsin-D (cath-D), urokinase plasminogen activator (uPA) and its specific inhibitor PAI-1 have shown an association with adverse prognosis in breast cancer. Our aim was to study the distribution of these markers in small axillary node-negative breast carcinomas using immunohistochemistry and relate the semiquantitative results to known prognostic factors, the expression of tenascin-C (Tn-C) in invasion border of the tumour and prognosis. All the 158 women (159 tumours) were treated with breast conserving surgery and postoperative radiotherapy. Cytoplasmic immunoreactivity for cath-D was seen in carcinoma cells in 47% and in stromal cells in 44%. Nearly all tumours expressed uPA and PAI-1, which were categorized to cytoplasmic expression in carcinoma cells and diffuse stromal expression and quantified – / + / ++ / +++ and further dichotomized for purposes of analysis. Expression of uPA and PAI-1 in stromal fibroblasts was recorded as – / +. Cytoplasmic and stromal cell cath-D contents were associated with grade, proliferation, Tn-C expression in the tumour invasion border and the development of distant metastasis. In multivariate analysis stromal cath-D proved to be an independent prognostic factor for metastasis. Stromal expression of uPA was associated with an increased risk of local recurrence; otherwise high levels of uPA did not associate with other prognostic factors nor with prognosis. Fibroblastic expression of PAI-1 showed an association with both local and distant disease recurrence. However, no consistent association between the immunohistochemically quantified uPA and PAI-1 and prognosis was found. In conclusion, immunohistochemical determination of cath-D seems to be a viable method to predict a higher risk of metastasis but not local recurrence in small axillary node-negative breast carcinomas.© 1999 Cancer Research Campaign
机译:组织蛋白酶D(cath-D),尿激酶纤溶酶原激活物(uPA)及其特异性抑制剂PAI-1的胞浆测定显示与乳腺癌不良预后相关。我们的目的是使用免疫组织化学研究这些标志物在小腋窝淋巴结阴性乳腺癌中的分布,并将半定量结果与已知的预后因素,腱鞘蛋白C(Tn-C)在肿瘤侵袭边界中的表达和预后相关联。所有158名妇女(159例肿瘤)均接受了保乳手术和术后放疗。 cath-D的细胞质免疫反应性在癌细胞中占47%,在基质细胞中占44%。几乎所有肿瘤都表达uPA和PAI-1,它们被分类为癌细胞中的胞质表达和弥漫性基质表达,并被定量– / ++ / ++ / ++++,并进一步分为两类进行分析。 uPA和PAI-1在基质成纤维细胞中的表达记录为– / +。细胞质和基质细胞cath-D的含量与肿瘤侵袭边界的分级,增殖,Tn-C表达和远处转移的发生有关。在多变量分析中,基质Cath-D被证明是转移的独立预后因素。 uPA的基质表达与局部复发的风险增加有关。否则,高水平的uPA与其他预后因素或预后均无关。 PAI-1的成纤维细胞表达与局部和远处疾病复发均相关。然而,在免疫组织化学定量的uPA和PAI-1与预后之间没有一致的关联。总之,免疫组化测定cath-D似乎是一种预测小的腋窝淋巴结阴性乳腺癌转移风险更高但局部复发的可行方法。©1999 Cancer Research Campaign

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