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本文引用的文献

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A novel approach for microRNA in situ hybridization using locked nucleic acid probes.一种使用锁核酸探针进行 miRNA 原位杂交的新方法。
Sci Rep. 2021 Feb 24;11(1):4504. doi: 10.1038/s41598-021-83888-5.
2
Plasma miR-21, miR-155, miR-10b, and Let-7a as the potential biomarkers for the monitoring of breast cancer patients.血浆 miR-21、miR-155、miR-10b 和 Let-7a 作为监测乳腺癌患者的潜在生物标志物。
Sci Rep. 2018 Dec 19;8(1):17981. doi: 10.1038/s41598-018-36321-3.
3
miRNAs as potential biomarkers in early breast cancer detection following mammography.微小RNA作为乳房X线摄影术后早期乳腺癌检测中的潜在生物标志物。
Cell Biosci. 2016 Jan 26;6:6. doi: 10.1186/s13578-016-0071-0. eCollection 2016.
4
Dysregulation of microRNAs in breast cancer and their potential role as prognostic and predictive biomarkers in patient management.乳腺癌中微小RNA的失调及其在患者管理中作为预后和预测生物标志物的潜在作用。
Breast Cancer Res. 2015 Feb 18;17:21. doi: 10.1186/s13058-015-0526-y.
5
Serum microRNA panel as biomarkers for early diagnosis of colorectal adenocarcinoma.血清微小RNA检测 panel作为结直肠癌早期诊断的生物标志物
Br J Cancer. 2014 Nov 11;111(10):1985-92. doi: 10.1038/bjc.2014.489. Epub 2014 Sep 18.
6
miR-638 mediated regulation of BRCA1 affects DNA repair and sensitivity to UV and cisplatin in triple-negative breast cancer.miR-638介导的BRCA1调控影响三阴性乳腺癌的DNA修复以及对紫外线和顺铂的敏感性。
Breast Cancer Res. 2014 Sep 17;16(5):435. doi: 10.1186/s13058-014-0435-5.
7
Oncogenic microRNAs: miR-155, miR-19a, miR-181b, and miR-24 enable monitoring of early breast cancer in serum.致癌性微小RNA:miR-155、miR-19a、miR-181b和miR-24可用于监测血清中的早期乳腺癌。
BMC Cancer. 2014 Jun 18;14:448. doi: 10.1186/1471-2407-14-448.
8
Different miRNA expression profiles between human breast cancer tumors and serum.人类乳腺癌肿瘤与血清之间不同的微小RNA表达谱。
Front Genet. 2014 May 27;5:149. doi: 10.3389/fgene.2014.00149. eCollection 2014.
9
Increased circulating microRNA-155 as a potential biomarker for breast cancer screening: a meta-analysis.循环中微小RNA-155水平升高作为乳腺癌筛查的潜在生物标志物:一项荟萃分析。
Molecules. 2014 May 16;19(5):6282-93. doi: 10.3390/molecules19056282.
10
microRNA-200c downregulates XIAP expression to suppress proliferation and promote apoptosis of triple-negative breast cancer cells.微小RNA-200c下调X连锁凋亡抑制蛋白表达以抑制三阴性乳腺癌细胞增殖并促进其凋亡。
Mol Med Rep. 2014 Jul;10(1):315-21. doi: 10.3892/mmr.2014.2222. Epub 2014 May 8.

miRNAs 作为早期乳腺癌检测的潜在生物标志物:系统评价。

MiRNAs as potential biomarkers in early breast cancer detection: a systematic review.

机构信息

Polizu Department, Alessandrescu-Rusescu National Institute for Mother and Child Health, Bucharest, Romania.

Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

出版信息

J Med Life. 2024 Jun;17(6):549-554. doi: 10.25122/jml-2024-0322.

DOI:10.25122/jml-2024-0322
PMID:39296436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11407494/
Abstract

Breast cancer remains a significant global health challenge, with high incidence and mortality rates. While mammography has contributed to declining mortality, its limitations in sensitivity and specificity for early detection, particularly in distinguishing between pure atypical ductal hyperplasia (ADH), ductal carcinoma in situ (DCIS), and invasive ductal carcinoma (IDC), highlight the need for more precise tools. Even with core needle biopsy (CNB), conclusive diagnoses often require surgical excision. This underscores the urgency for non-invasive biomarkers to improve early detection and differentiation, potentially reducing invasive procedures. Recent research has shifted focus from mRNA to microRNAs (miRNAs) as promising biomarkers for breast cancer screening. These small non-coding RNAs, which exhibit abnormal expression patterns in breast cancer patients' tissue and serum/plasma, play crucial roles in early breast cancer development by modulating proto-oncogenes or tumor suppressor genes at the post-transcriptional level. Notably, miRNAs such as miR-21, miR-155, and miR-200c are key regulators of cell proliferation and apoptosis, with the potential to distinguish between normal tissue and various stages of breast lesions, including ADH, DCIS, and IDC. Additionally, miRNAs in serum and plasma offer a non-invasive method to differentiate breast cancer stages. This review aims to consolidate current knowledge on early breast lesions and explore the potential of miRNAs as biomarkers for early breast cancer detection, which could enhance risk prediction and reduce reliance on invasive diagnostic procedures.

摘要

乳腺癌仍然是一个重大的全球健康挑战,具有高发病率和死亡率。虽然乳房 X 线照相术有助于降低死亡率,但它在早期检测方面的敏感性和特异性有限,特别是在区分单纯非典型导管增生 (ADH)、导管原位癌 (DCIS) 和浸润性导管癌 (IDC) 方面,突出了需要更精确的工具。即使进行了核心针活检 (CNB),明确的诊断通常仍需要手术切除。这突显了需要非侵入性生物标志物来改善早期检测和区分,从而可能减少侵入性程序。最近的研究已经将重点从 mRNA 转移到 microRNAs (miRNAs),作为乳腺癌筛查的有前途的生物标志物。这些小的非编码 RNA 在乳腺癌患者的组织和血清/血浆中表现出异常表达模式,通过在转录后水平调节原癌基因或肿瘤抑制基因,在早期乳腺癌的发展中发挥关键作用。值得注意的是,miR-21、miR-155 和 miR-200c 等 miRNA 是细胞增殖和凋亡的关键调节剂,有可能区分正常组织和各种乳腺病变阶段,包括 ADH、DCIS 和 IDC。此外,血清和血浆中的 miRNA 提供了一种非侵入性的方法来区分乳腺癌的阶段。本综述旨在整合关于早期乳腺病变的现有知识,并探讨 miRNA 作为早期乳腺癌检测生物标志物的潜力,这可能增强风险预测并减少对侵入性诊断程序的依赖。