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miR-34 在癌症药物耐药性中的作用。

The role of miR-34 in cancer drug resistance.

机构信息

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Cancer and Inflammation Research, Institute for Molecular Medicine, University of Southern Denmark, Odense, Denmark.

出版信息

J Cell Physiol. 2020 Oct;235(10):6424-6440. doi: 10.1002/jcp.29640. Epub 2020 Feb 16.


DOI:10.1002/jcp.29640
PMID:32064620
Abstract

Resistance to conventional chemotherapy remains a major cause of cancer relapse and cancer-related deaths. Therefore, there is an urgent need to overcome resistance barriers. To improve cancer treatment approaches, it is critical to elucidate the basic mechanisms underlying drug resistance. Increasingly, the mechanisms involving micro-RNAs (miRNAs) are studied because miRNAs are also considered practical therapeutic options due to high degrees of specificity, efficacy, and accuracy, as well as their ability to target multiple genes at the same time. Years of research have firmly established miR-34 as a key tumor suppressor miRNA whose target genes are involved in drug resistance mechanisms. Indeed, numerous articles show that low levels of circulating miR-34 or tumor-specific miR-34 expression are associated with poor response to chemotherapy. In addition, elevation of inherently low miR-34 levels in resistant cancer cells effectively restores sensitivity to chemotherapeutic agents. Here, we review this literature, also highlighting some contradictory observations. In addition, we discuss the potential utility of miR-34 expression as a predictive biomarker for chemotherapeutic drug response. Although caution needs to be exercised, miR-34 is emerging as a biomarker that could improve cancer precision medicine.

摘要

对常规化疗的耐药性仍然是癌症复发和癌症相关死亡的主要原因。因此,迫切需要克服耐药性障碍。为了改进癌症治疗方法,阐明耐药性的基本机制至关重要。由于 miRNA 具有高度的特异性、疗效和准确性,并且能够同时靶向多个基因,因此越来越多的研究涉及 miRNA 的机制。多年的研究已经明确确立了 miR-34 作为关键的肿瘤抑制 miRNA,其靶基因参与耐药机制。事实上,许多文章表明,循环 miR-34 水平低或肿瘤特异性 miR-34 表达水平低与对化疗反应不佳有关。此外,在耐药癌细胞中升高固有低水平的 miR-34 可有效恢复对化疗药物的敏感性。在这里,我们回顾了这方面的文献,同时也强调了一些相互矛盾的观察结果。此外,我们还讨论了 miR-34 表达作为化疗药物反应预测生物标志物的潜在用途。尽管需要谨慎行事,但 miR-34 作为一种生物标志物正在出现,它可以改善癌症精准医学。

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引用本文的文献

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Redesigning miR-34a: structural and chemical advances in the therapeutic development of an miRNA anti-cancer agent.

Biochem Soc Trans. 2025-8-4

[2]
m6A reader IGF2BP2-stabilized lncRNA LHX1-DT inhibits renal cell carcinoma (RCC) cell proliferation and invasion by sponging miR-590-5p.

NPJ Precis Oncol. 2025-6-17

[3]
Nanoliposomes as nonviral vectors in cancer gene therapy.

MedComm (2020). 2024-6-25

[4]
Mapping the function of MicroRNAs as a critical regulator of tumor-immune cell communication in breast cancer and potential treatment strategies.

Front Cell Dev Biol. 2024-4-25

[5]
is a promising prognostic, immunological, and therapeutic biomarker in human tumors.

Biochem Biophys Rep. 2024-5-1

[6]
The microRNA-34 Family and Its Functional Role in Lung Cancer.

Am J Clin Oncol. 2024-9-1

[7]
Joint global and local interpretation method for CIN status classification in breast cancer.

Heliyon. 2024-2-28

[8]
The Expression of miR-34c-5p Induces G0/G1 Cell Cycle Arrest and Apoptosis in SW480 Colon Cancer Cell.

Iran J Pharm Res. 2023-6-18

[9]
Restoring microRNA-34a overcomes acquired drug resistance and disease progression in human breast cancer cell lines via suppressing the ABCC1 gene.

Breast Cancer Res Treat. 2024-2

[10]
MicroRNA-34 Family in Cancers: Role, Mechanism, and Therapeutic Potential.

Cancers (Basel). 2023-9-26

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