The overexpressed microRNAs miRs-182, 155, 493, 454 and U6 snRNA, and underexpressed let-7c, miR-328 and miR-451a as potential biomarkers in invasive breast cancer and their clinicopathological significance.

IF 2.5 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2024-08-12 DOI:10.1159/000540863
Luděk Záveský, Eva Jandáková, Vit Weinberger, Luboš Minář, Milada Kohoutová, Adela Tefr Faridova, Ondrej Slanar
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引用次数: 0

Abstract

Introduction Breast cancer comprises the leading cause of cancer-related death in women. MicroRNAs (miRNAs) have emerged as important factors with concern to carcinogenesis and have potential for use as biomarkers. Methods This study provides a comprehensive evaluation of the microRNA expression in invasive breast carcinoma of no special type tissues compared with benign tissues via large-scale screening and the candidate-specific validation of 15 miRNAs and U6 snRNA applying qPCR and the examination of clinicopathological data. Results Of the six downregulated miRNAs, let-7c was identified as the most promising miRNA biomarker and its lower expression was linked with Ki-67 positivity, luminal B versus luminal A samples, multifocality, lymph-node metastasis and inferior PFS. Of the 9 upregulated sncRNAs, the data on U6 snRNA, miR-493 and miR-454 highlighted their potential oncogenic functions. An elevated U6 snRNA expression was associated with the tumor grade, Ki-67 positivity, luminal B versus A samples, lymph-node metastasis and worsened PFS (and OS) outcomes. An elevated miR-454 expression was detected in higher grades, Ki-67 positive and luminal B versus A samples. Higher miR-493 levels were noted for the tumor stage (and grade) and worse patient outcomes (PFS, OS). The data also suggested that miR-451a and miR-328 may have tumor suppressor roles, and miR-182 and miR-200c pro-oncogenic functions, while the remaining sncRNAs did not evince any significant associations. Conclusion We showed particular microRNAs and U6 snRNA as differentially expressed between tumors and benign tissues and associated with clinicopathological parameters thus potentially corresponding with important roles in breast carcinogenesis. Their importance should be further investigated and evaluated in follow-up studies to reveal their potential in clinical practice.

作为浸润性乳腺癌潜在生物标志物的过表达 microRNA miRs-182、155、493、454 和 U6 snRNA,以及表达不足的 let-7c、miR-328 和 miR-451a 及其临床病理学意义。
导言 乳腺癌是女性因癌症死亡的主要原因。微 RNA(miRNA)已成为致癌的重要因素,并有可能用作生物标志物。方法 本研究通过对 15 个 miRNA 和 U6 snRNA 进行大规模筛选和候选特异性验证,并应用 qPCR 和临床病理数据检查,全面评估了无特殊类型浸润性乳腺癌组织与良性组织相比的 microRNA 表达情况。结果 在6个下调的miRNA中,let-7c被确定为最有希望的miRNA生物标志物,其较低的表达与Ki-67阳性、管腔B样本与管腔A样本、多灶性、淋巴结转移和较差的PFS有关。在9个上调的sncRNA中,有关U6 snRNA、miR-493和miR-454的数据强调了它们潜在的致癌功能。U6 snRNA表达的升高与肿瘤分级、Ki-67阳性、管腔B样本相对于A样本、淋巴结转移以及PFS(和OS)结果恶化有关。在分级较高、Ki-67 阳性和管腔 B 与管腔 A 样本中检测到 miR-454 表达升高。在肿瘤分期(和分级)和患者预后(PFS、OS)较差的情况下,miR-493水平较高。数据还表明,miR-451a 和 miR-328 可能具有肿瘤抑制作用,miR-182 和 miR-200c 具有促癌功能,而其余的 sncRNAs 则没有发现任何显著的关联。结论 我们发现某些 microRNA 和 U6 snRNA 在肿瘤和良性组织之间有差异表达,并与临床病理参数相关,因此可能在乳腺癌发生过程中发挥重要作用。应在后续研究中进一步调查和评估它们的重要性,以揭示它们在临床实践中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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