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Synergistic miRNA Combinations Mitigate Doxorubicin-Induced Cardiotoxicity: Are We Ready for Clinical Translation?

作者信息

Sepúlveda Pilar

机构信息

Regenerative Medicine and Heart Transplantation Unit, Health Research Institute Hospital la Fe, Valencia, Spain; Hospital Universitari i Politècnic La Fe, Valencia, Spain; Department of Pathology, University of Valencia, Valencia, Spain; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares, Carlos III Institute of Health, Madrid, Spain.

出版信息

JACC CardioOncol. 2025 Jun;7(4):411-413. doi: 10.1016/j.jaccao.2025.04.002.

DOI:10.1016/j.jaccao.2025.04.002
PMID:40537189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12228129/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b08/12228129/63742d3a5077/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b08/12228129/63742d3a5077/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b08/12228129/63742d3a5077/ga1.jpg

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本文引用的文献

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2
Modeling Cardiotoxicity in Pediatric Oncology Patients Using Patient-Specific iPSC-Derived Cardiomyocytes Reveals Downregulation of Cardioprotective microRNAs.使用患者特异性诱导多能干细胞衍生的心肌细胞对儿科肿瘤患者的心脏毒性进行建模,揭示了心脏保护微小RNA的下调。
Antioxidants (Basel). 2023 Jul 3;12(7):1378. doi: 10.3390/antiox12071378.
3
MicroRNA-4732-3p Is Dysregulated in Breast Cancer Patients with Cardiotoxicity, and Its Therapeutic Delivery Protects the Heart from Doxorubicin-Induced Oxidative Stress in Rats.
微小RNA-4732-3p在患有心脏毒性的乳腺癌患者中表达失调,其治疗性递送可保护大鼠心脏免受阿霉素诱导的氧化应激损伤。
Antioxidants (Basel). 2022 Sep 30;11(10):1955. doi: 10.3390/antiox11101955.
4
Novel antisense therapy targeting microRNA-132 in patients with heart failure: results of a first-in-human Phase 1b randomized, double-blind, placebo-controlled study.针对心力衰竭患者的新型靶向微小RNA-132反义疗法:首例人体1b期随机、双盲、安慰剂对照研究结果
Eur Heart J. 2021 Jan 7;42(2):178-188. doi: 10.1093/eurheartj/ehaa898.
5
A Three-Way Combinatorial CRISPR Screen for Analyzing Interactions among Druggable Targets.一种用于分析可成药靶点之间相互作用的三向组合CRISPR筛选
Cell Rep. 2020 Aug 11;32(6):108020. doi: 10.1016/j.celrep.2020.108020.
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