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微小RNA-10b作为转移性乳腺癌的临床标志物和治疗靶点

miR-10b as a Clinical Marker and a Therapeutic Target for Metastatic Breast Cancer.

作者信息

Halim Alan, Kim Bryan, Kenyon Elizabeth, Moore Anna

机构信息

Precision Health Program, Michigan State University, East Lansing, MI, USA.

Department of Radiology, College of Human Medicine, Michigan State University, East Lansing, MI, USA.

出版信息

Technol Cancer Res Treat. 2025 Jan-Dec;24:15330338251339256. doi: 10.1177/15330338251339256. Epub 2025 May 21.

DOI:10.1177/15330338251339256
PMID:40397123
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12099151/
Abstract

Despite advances in cancer detection and treatment, metastatic breast cancer continues to carry a poor prognosis due to the lack of diagnostic and therapeutic resources that are specific to the metastatic process. MicroRNA-10b (miR-10b) is a small, noncoding RNA that is the focus of many studies due to its unique role as a driver of metastasis. The pathways it is involved in and the properties it confers have been reviewed previously and, collectively, are suggestive of the potential of miR-10b as a clinical marker and as a therapeutic target specific to metastatic disease. With the goal of application of our understanding of miR-10b to the clinic, in this mini-review, we highlight the studies that support the utility of miR-10b for these translational purposes.

摘要

尽管在癌症检测和治疗方面取得了进展,但由于缺乏针对转移过程的诊断和治疗资源,转移性乳腺癌的预后仍然很差。微小RNA-10b(miR-10b)是一种小的非编码RNA,由于其作为转移驱动因子的独特作用而成为许多研究的焦点。它所涉及的途径及其赋予的特性此前已有综述,总体而言,提示了miR-10b作为临床标志物和转移性疾病特异性治疗靶点的潜力。为了将我们对miR-10b的理解应用于临床,在本综述中,我们重点介绍了支持miR-10b用于这些转化目的的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4734/12099151/f6656e3e39e1/10.1177_15330338251339256-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4734/12099151/f6656e3e39e1/10.1177_15330338251339256-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4734/12099151/f6656e3e39e1/10.1177_15330338251339256-fig1.jpg

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本文引用的文献

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Circulating miR-10b, soluble urokinase-type plasminogen activator receptor, and plasminogen activator inhibitor-1 as predictors of non-small cell lung cancer progression and treatment response.循环 miR-10b、可溶性尿激酶型纤溶酶原激活物受体和纤溶酶原激活物抑制剂-1 作为非小细胞肺癌进展和治疗反应的预测指标。
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Organotypic 3D Cell-Architecture Impacts the Expression Pattern of miRNAs-mRNAs Network in Breast Cancer SKBR3 Cells.器官型3D细胞结构影响乳腺癌SKBR3细胞中miRNA-mRNA网络的表达模式。
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Circulating microRNAs can predict chemotherapy-induced toxicities in patients being treated for primary breast cancer.
循环 microRNAs 可预测原发性乳腺癌患者化疗引起的毒性。
Breast Cancer Res Treat. 2023 Nov;202(1):73-81. doi: 10.1007/s10549-023-07033-8. Epub 2023 Aug 4.
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MicroRNA: trends in clinical trials of cancer diagnosis and therapy strategies.微小 RNA:癌症诊断和治疗策略临床试验的趋势。
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Co-administration of temozolomide (TMZ) and the experimental therapeutic targeting miR-10b, profoundly affects the tumorigenic phenotype of human glioblastoma cells.替莫唑胺(TMZ)与靶向miR-10b的实验性治疗药物联合使用,会对人胶质母细胞瘤细胞的致瘤表型产生深远影响。
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Enhancing the Management of Metastatic Tumors by Robust Co-Delivery of 5-Fluorouracil/MicroRNA-10b Inhibitor Using EGFR-Targeted Nanovehicles.利用 EGFR 靶向纳米载体实现 5-氟尿嘧啶/微小 RNA-10b 抑制剂的稳健共递药,增强转移性肿瘤的管理。
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