Abstract |
Chemotherapy related cardiotoxicity is now becoming one of the biggest hurdles for the prognosis of cancer patients. Therapeutically delivering protective small RNAs holds promise for the cardiotoxicity prevention and therapy. However, heart is intrinsically refractory to the nanoparticle-mediated drug delivery. In this study, we found that the exosome-mediated miRNA delivery into the heart could be significantly augmented with the aid of ultrasound targeted microbubble destruction (UTMD). Moreover, we found that UTMD assisted exosomal miR-21 delivery into the heart significantly decreased the cell death, and restored the cardiac function in a doxorubicin induced cardiotoxicity mouse model. Our study here not only provides a promising strategy to protect the heart from the chemotherapy related cardiotoxicity, but also sheds light on gene therapy of other heart diseases.
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Authors | Wenqi Sun, Ping Zhao, Yonggang Zhou, Changyang Xing, Lianbi Zhao, Zhelong Li, Lijun Yuan |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 532
Issue 1
Pg. 60-67
(10 29 2020)
ISSN: 1090-2104 [Electronic] United States |
PMID | 32828538
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2020 Elsevier Inc. All rights reserved. |
Chemical References |
- Antibiotics, Antineoplastic
- Cardiotonic Agents
- MIRN21 microRNA, mouse
- MicroRNAs
- Doxorubicin
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Topics |
- Animals
- Antibiotics, Antineoplastic
(toxicity)
- Apoptosis
- Cardiotonic Agents
(administration & dosage)
- Cardiotoxicity
(pathology, physiopathology, prevention & control)
- Cell Death
- Disease Models, Animal
- Doxorubicin
(toxicity)
- Drug Delivery Systems
- Echocardiography, Doppler, Pulsed
- Exosomes
- Heart Function Tests
- Humans
- Male
- Mice
- Mice, Inbred C57BL
- MicroRNAs
(administration & dosage, genetics)
- Microbubbles
- Ultrasonics
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