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循环游离 DNA、p53 抗体和 KRAS 基因突变与子宫内膜癌。

Circulating free DNA, p53 antibody and mutations of KRAS gene in endometrial cancer.

机构信息

Department of Obstetrics and Gynecology, Medical University of Bialystok, Bialystok, Poland.

出版信息

Int J Cancer. 2010 Aug 1;127(3):612-21. doi: 10.1002/ijc.25077.

DOI:10.1002/ijc.25077
PMID:19960433
Abstract

This study was conducted to evaluate the significance of circulating free DNA (CFDNA), p53 antibody (p53-Ab) and mutations of KRAS gene in the development of endometrial cancer (EC). A total of 109 patients with EC (87 patients with Type I and 22 patients with Type II) took part in this study. KRAS mutations and CFDNA were detected by means of the PCR-RFLP and enriched by the PCR-RFPL method. ELISA was used to analyze plasma p53-Ab. Tissue expression of P53 protein was evaluated immunohistochemically (IHC). The frequency of KRAS mutations was especially high in Grade 2 of Type I EC. CFDNA was frequently detected in patients with early stage of Type II EC at a low level of grade. It is noteworthy that the p53-Ab positive rate increased in the higher grade of Type I tumors. A significant difference in the number of cases with the p53-Ab was found in the advanced stage of Type I tumors. The frequency of KRAS and p53-Ab correlates with tumor stage only in the Type I EC. Plasma CFDNA and p53-Ab offer a chance to develop a procedure for EC Type II diagnosis. The association between tumor cells related to CFDNA and p53-Ab with Type II tumor suggests that it might potentially serve as a marker in predicting the prognosis and offers a possibility to individualize treatment regimen.

摘要

本研究旨在评估循环游离 DNA (cfDNA)、p53 抗体 (p53-Ab) 和 KRAS 基因突变在子宫内膜癌 (EC) 发展中的意义。共有 109 例 EC 患者(87 例 I 型和 22 例 II 型)参与了这项研究。通过 PCR-RFLP 检测 KRAS 基因突变,通过 PCR-RFPL 法富集 cfDNA。采用 ELISA 法分析血浆 p53-Ab。采用免疫组化 (IHC) 法评估 P53 蛋白的组织表达。I 型 EC 中 2 级的 KRAS 突变频率特别高。cfDNA 在 II 型 EC 早期、分级较低的患者中经常被检测到。值得注意的是,I 型肿瘤中,p53-Ab 阳性率随肿瘤分级的升高而增加。在 I 型肿瘤的晚期,p53-Ab 阳性的病例数有显著差异。KRAS 和 p53-Ab 的频率仅与 I 型 EC 的肿瘤分期相关。血浆 cfDNA 和 p53-Ab 为 II 型 EC 的诊断提供了一个机会。与 cfDNA 和 p53-Ab 相关的肿瘤细胞与 II 型肿瘤的相关性表明,它可能作为预测预后的标志物,并为个体化治疗方案提供了可能。

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