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[血管生成拟态与卵巢癌临床病理特征及预后的相关性]

[Correlation of vasculogenic mimicry with clinicopathologic features and prognosis of ovarian carcinoma].

作者信息

Gao Yan, Zhao Xiu-lan, Gu Qiang, Wang Jun-yan, Zhang Shi-wu, Zhang Dan-fang, Wang Xing-hui, Zhao Nan, Gao Yu-tong, Sun Bao-cun

机构信息

Department of Pathology, Tianjin Medical University, Tianjin 300070, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2009 Sep;38(9):585-9.

Abstract

OBJECTIVE

To explore the existence of vasculogenic mimicry (VM) in ovarian carcinoma and its correlationship with the clinicopathologic features and prognosis of the tumor.

METHODS

A total of 84 ovarian carcinoma cases were collected with complete clinical and prognostic data. CD31 immunohistochemistry and PAS special stain were used to investigate VM in the tumor tissue. Immunohistochemical staining of VEGF, MMP-2, MMP-9, E-cadherin, beta-catenin, and Vimentin were used to explore the pathogenesis of VM.

RESULTS

Totally 36 of 84 cases exhibited evidence of VM. FIGO classification, pathologic grades and histological types were significantly different between the VM and non-VM groups. Expression of VEGF, MMP-2, MMP-9, E-cadherin and beta-catenin were higher in the VM group than in the non-VM group. Kaplan-Meier survival curve analysis showed that cases of the VM group had a lower survival rate than that of the non-VM group (P = 0.04).

CONCLUSIONS

Vasculogenic mimicry exists in ovarian carcinoma. Ovarian carcinomas with a high grade malignancy have a high incidence of VM formation, a higher incidence of metastases and a lower survival rate. High expression of MMP-2 and MMP-9 may contribute to the formation of VM in the ovarian cancer.

摘要

目的

探讨卵巢癌中血管生成拟态(VM)的存在情况及其与肿瘤临床病理特征和预后的相关性。

方法

收集84例具有完整临床和预后资料的卵巢癌病例。采用CD31免疫组织化学和PAS特殊染色法检测肿瘤组织中的VM。采用VEGF、MMP-2、MMP-9、E-钙黏蛋白、β-连环蛋白和波形蛋白的免疫组织化学染色法探讨VM的发病机制。

结果

84例病例中共有36例显示有VM证据。VM组与非VM组之间的国际妇产科联盟(FIGO)分期、病理分级和组织学类型有显著差异。VM组中VEGF、MMP-2、MMP-9、E-钙黏蛋白和β-连环蛋白的表达高于非VM组。Kaplan-Meier生存曲线分析显示,VM组病例的生存率低于非VM组(P = 0.04)。

结论

卵巢癌中存在血管生成拟态。恶性程度高的卵巢癌VM形成发生率高、转移发生率高且生存率低。MMP-2和MMP-9的高表达可能有助于卵巢癌中VM的形成。

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