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三阴性乳腺癌的新型预后和预测性微小RNA靶点

Novel prognostic and predictive microRNA targets for triple-negative breast cancer.

作者信息

Turashvili Gulisa, Lightbody Elizabeth D, Tyryshkin Kathrin, SenGupta Sandip K, Elliott Bruce E, Madarnas Yolanda, Ghaffari Abdi, Day Andrew, Nicol Christopher J B

机构信息

Kingston Health Sciences Centre, Kingston, Ontario, Canada.

Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.

出版信息

FASEB J. 2018 May 29:fj201800120R. doi: 10.1096/fj.201800120R.

Abstract

Triple-negative breast cancers (TNBCs) account for ∼25% of all invasive carcinomas and represent a large subset of aggressive, high-grade tumors. Despite current research focused on understanding the genetic landscape of TNBCs, reliable prognostic and predictive biomarkers remain limited. Although dysregulated microRNAs (miRNAs) have emerged as key players in many cancer types, the role of miRNAs in TNBC disease progression is unclear. We performed miRNA profiling of 51 TNBCs by next-generation sequencing to reveal differentially expressed miRNAs. A total of 228 miRNAs were identified. Three miRNAs (miR-224-5p, miR-375, and miR-205-5p) separated the tumors based on basal status. Six miRNAs (high let-7d-3p, miR-203b-5p, and miR-324-5p; low miR-30a-3p, miR-30a-5p, and miR-199a-5p) were significantly associated with decreased overall survival (OS) and 5 miRNAs (high let-7d-3p; low miR-30a-3p, miR-30a-5p, miR-30c-5p, and miR-128-3p) with decreased relapse-free survival (RFS). On multivariate analysis, high expression of let-7d-3p and low expression of miR-30a were independent predictors of decreased OS and RFS. High expression of miR-95-3p was significantly associated with decreased OS and RFS in patients treated with anthracycline-based chemotherapy. Five miRNAs (let-7d-3p, miR-30a-3p, miR-30c-5p, miR-128-3p, and miR-95-3p) were validated by quantitative RT-PCR. Our findings unveil novel prognostic and predictive miRNA targets for TNBC, including a miRNA signature that predicts patient response to anthracycline-based chemotherapy. This may improve clinical management and/or lead to the development of novel therapies.-Turashvili, G., Lightbody, E. D., Tyryshkin, K., SenGupta, S. K., Elliott, B. E., Madarnas, Y., Ghaffari, A., Day, A., Nicol, C. J. B. Novel prognostic and predictive microRNA targets for triple-negative breast cancer.

摘要

三阴性乳腺癌(TNBC)占所有浸润性癌的约25%,是侵袭性高级别肿瘤的一个很大的子集。尽管目前的研究集中在了解TNBC的基因图谱,但可靠的预后和预测生物标志物仍然有限。虽然失调的微小RNA(miRNA)已成为许多癌症类型中的关键因素,但miRNA在TNBC疾病进展中的作用尚不清楚。我们通过下一代测序对51例TNBC进行了miRNA谱分析,以揭示差异表达的miRNA。共鉴定出228种miRNA。三种miRNA(miR-224-5p、miR-375和miR-205-5p)根据基底状态区分肿瘤。六种miRNA(高let-7d-3p、miR-203b-5p和miR-324-5p;低miR-30a-3p、miR-30a-5p和miR-199a-5p)与总生存期(OS)降低显著相关,五种miRNA(高let-7d-3p;低miR-30a-3p、miR-30a-5p、miR-30c-5p和miR-128-3p)与无复发生存期(RFS)降低相关。多变量分析显示,let-7d-3p高表达和miR-30a低表达是OS和RFS降低的独立预测因素。在接受蒽环类化疗的患者中,miR-95-3p高表达与OS和RFS降低显著相关。通过定量RT-PCR验证了五种miRNA(let-7d-3p、miR-30a-3p、miR-30c-5p、miR-128-3p和miR-95-3p)。我们的研究结果揭示了TNBC新的预后和预测性miRNA靶点,包括一种预测患者对蒽环类化疗反应的miRNA特征。这可能会改善临床管理和/或导致新疗法的开发。-图拉什维利,G.,莱特博迪,E.D.,季里什金,K.,森古普塔,S.K.,埃利奥特,B.E.,马达纳斯,Y.,加法里,A.,戴,A.,尼科尔,C.J.B.三阴性乳腺癌新的预后和预测性微小RNA靶点。

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