子宫内膜癌中胰岛素样生长因子 II mrna 结合蛋白 3 (IMP3) 的表达与预后和形态学因素的关系。

Silas Otero Reis Salum, Eduardo Batista Candido, Maria Aparecida Custódio Domingues, Elida Paula Benquique Ojopi, Ângela Favorito Santarem Tonon, Agnaldo Lopes da Silva-Filho
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引用次数: 0

摘要

目的:子宫内膜癌(EC)是一种异质性疾病,复发率在 15% 到 20% 之间。区分预后较差的病例在一定程度上是为了缩短预后较好病例的手术分期时间。本研究旨在评估EC中胰岛素样生长因子II mRNA结合蛋白3(IMP3)表达与预后和形态学因素之间的关联:这项回顾性、横断面分析研究包括79例EC患者(70例子宫内膜样癌(EEC)和9例浆液性癌(SC))和74例良性子宫内膜对照组。通过基于免疫组化的 TMA(组织芯片)评估了 IMP3 的表达,并将结果与形态学和预后因素(包括 claudins 3 和 4、雌激素和孕激素受体、TP53 和 KI67)相关联:结果:在两种程度上,IMP3在SC中的表达均明显高于在EEC中的表达(p结论:IMP3的表达与较差的预后相关:IMP3的表达与所研究的较差预后因素有关。这些发现表明,IMP3可能是EC预后较差的潜在生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of insulin-like growth factor II mrna-binding protein 3 (IMP3) expression with prognostic and morphological factors in endometrial cancer.

Objective: Endometrial cancer (EC) is a heterogeneous disease with recurrence rates ranging from 15 to 20%. The discrimination of cases with a worse prognosis aims, in part, to reduce the length of surgical staging in cases with a better prognosis. This study aimed to evaluate the association between Insulin-like growth factor II mRNA-binding protein 3 (IMP3) expression and prognostic and morphological factors in EC.

Methods: This retrospective, cross-sectional, analytical study included 79 EC patients - 70 endometrioid carcinoma (EEC) and 9 serous carcinoma (SC) - and 74 benign endometrium controls. IMP3 expression was evaluated by immunohistochemistry-based TMA (Tissue Microarray), and the results were associated with morphological and prognostic factors, including claudins 3 and 4, estrogen and progesterone receptors, TP53, and KI67.

Results: IMP3 expression was significantly higher in SC compared to EEC in both extent (p<0.001) and intensity (p=0.044). It was also significantly associated with worse prognostic factors, including degree of differentiation (p=0.024, p<0.001), staging (p<0.001; p<0.001) and metastasis (p=0.002; p<0.001). IMP3 expression was also significant in extent (p=0.002) in endometrial tumors compared with controls. In addition, protein TP53 and KI67 showed significant associations in extent and intensity, respectively.

Conclusion: IMP3 expression was associated with worse prognostic factors studied. These findings suggest that IMP3 may be a potential biomarker for EC poorer prognosis.

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