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表皮生长因子受体、E-钙黏蛋白和基质金属蛋白酶-9 在卵巢上皮性癌中的免疫组织化学表达及其与患者死亡的关系。

Immunohistochemical expression of epidermal growth factor receptor, E-cadherin, and matrix metalloproteinase-9 in ovarian epithelial cancer and relation to patient deaths.

机构信息

Faculty of Medicine, Department of Pathology, Tanta University, Tanta, Egypt.

出版信息

Ann Diagn Pathol. 2010 Dec;14(6):387-95. doi: 10.1016/j.anndiagpath.2010.05.005. Epub 2010 Aug 14.

DOI:10.1016/j.anndiagpath.2010.05.005
PMID:21074685
Abstract

Ovarian cancer is the most frequent cause of death from gynecologic cancer in the world. Current prognostic factors do not allow reliable prediction of response to chemotherapy and survival for individual ovarian cancer patients. Epidermal growth factor receptor (EGFR), E-cadherin, and matrix metalloproteinase (MMP)-9 are frequently studied in cancer; but their prognostic value in ovarian carcinoma remains unclear. In this study, we investigated the immunohistochemical expression of EGFR, E-cadherin, and MMP-9 in 120 cases of ovarian epithelial carcinoma; their relation to each other; their relation to histologic type, grade, and stage; and their relation to death rates after 3years of follow-up. Our results show that EGFR and MMP-9 were overexpressed extensively in high grades and advanced stages especially in nonserous carcinomas. E-cadherin was gradually lost in advanced cancers. There was a positive relation between the 3 antibodies and between them and the death rates. There is a strong relationship between EGFR and MMP-9, and this relation may occur by affecting E-cadherin. The present study provides a rationale for evaluating drugs that target these new pathways that may be promising in ovarian cancer treatment.

摘要

卵巢癌是全球妇科癌症死亡的最常见原因。目前的预后因素不能可靠地预测个别卵巢癌患者对化疗的反应和生存。表皮生长因子受体(EGFR)、E-钙黏蛋白和基质金属蛋白酶(MMP)-9 在癌症中经常被研究;但它们在卵巢癌中的预后价值仍不清楚。在这项研究中,我们研究了 120 例卵巢上皮癌中 EGFR、E-钙黏蛋白和 MMP-9 的免疫组织化学表达;它们之间的关系;它们与组织学类型、分级和分期的关系;以及与 3 年随访后死亡率的关系。我们的结果表明,EGFR 和 MMP-9 在高级别和晚期,特别是在非浆液性癌中广泛过表达。E-钙黏蛋白在晚期癌症中逐渐丢失。这 3 种抗体之间以及它们与死亡率之间存在正相关关系。EGFR 和 MMP-9 之间存在很强的关系,这种关系可能通过影响 E-钙黏蛋白而发生。本研究为评估针对这些新途径的药物提供了依据,这些药物可能在卵巢癌治疗中具有广阔的前景。

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