子宫内膜癌预后分子生物标志物研究进展。

Journal of cancer research & therapy Pub Date : 2019-12-01 Epub Date: 2019-12-03 DOI:10.14312/2052-4994.2019-3
J Edgardo Hernández, Ailyn González-Montiel, Jesús C Ceb Allos-Villalva, David Cantú, Salim Barquet, Anny Olivares-Mundo, Luis A Herrera, Diddier Prada
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引用次数: 8

摘要

背景:子宫内膜癌(EC)是全球第四大最常见的女性恶性肿瘤,也是发达国家最常见的妇科癌症。子宫内膜样亚型经常规治疗预后良好;然而,复发降低了总生存率。目的:描述有关可能预测EC总生存期(OS)、无复发生存期(RFS)和癌症特异性生存期(CSS)的潜在分子生物标志物的最相关证据。方法:在PUBMED中搜索子宫内膜癌、分子生物标志物和生存率。我们选择了2000年1月至2016年12月期间发表的关于子宫内膜癌、分子生物标志物和生存分析的英文原创文章。结果:一些分子预后生物标志物已经在子宫内膜癌妇女的生存和治疗反应方面进行了研究;激素受体、microrna和其他分子已成为潜在有用的生物标志物,包括HER2、p21、HE4、PTEN、p27、ANCCA和ANXA2。结论:在评估OS、RFS和CSS时使用生物标志物需要大量的试验来扩大我们对子宫内膜癌变的理解。一些分子标记与EC的高肿瘤分级和晚期临床阶段显著相关,因此,当联合使用时可能具有累加效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prognostic molecular biomarkers in endometrial cancer: A review.

Prognostic molecular biomarkers in endometrial cancer: A review.

Prognostic molecular biomarkers in endometrial cancer: A review.

Prognostic molecular biomarkers in endometrial cancer: A review.

Background: Endometrial cancer (EC) is the fourth most common malignancy in women worldwide and the most common gynecological cancer in developed countries. The endometrioid subtype has an excellent prognosis with conventional treatment; however, recurrence reduces overall survival.

Objective: Describe the most relevant evidence regarding selected potential molecular biomarkers that may predict overall survival (OS), relapse-free survival (RFS), and cancer-specific survival (CSS) in EC.

Methods: An exhaustive search was performed in PUBMED with the search terms endometrial cancer, molecular biomarker, and survival. We selected original articles written in English about endometrial cancer, molecular biomarkers, and that included survival analysis published between January 2000 and December 2016.

Results: Several molecular prognostic biomarkers have been studied in terms of survival and therapeutic response in women with endometrial cancer; hormone receptors, microRNAs, and other molecules have emerged as potentially useful biomarkers, including HER2, p21, HE4, PTEN, p27, ANCCA, and ANXA2.

Conclusions: The use of biomarkers in the assessment of OS, RFS, and CSS requires large trials to expand our understanding of endometrial carcinogenesis. Several molecular markers are significantly associated with a high tumor grade and advanced clinical stage in EC and, therefore, could have additive effects when combined.

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