Free Radical Biology and Medicine, Journal Year: 2024, Volume and Issue: 223, P. 224 - 236
Published: Aug. 6, 2024
Language: Английский
Free Radical Biology and Medicine, Journal Year: 2024, Volume and Issue: 223, P. 224 - 236
Published: Aug. 6, 2024
Language: Английский
Frontiers in Molecular Biosciences, Journal Year: 2023, Volume and Issue: 10
Published: Aug. 3, 2023
Doxorubicin (DOX) is an extensively used chemotherapeutic agent that can cause severe and frequent cardiotoxicity, which limits its clinical application. Although there have been extensive researches on the cardiotoxicity caused by DOX, still a lack of effective treatment. It necessary to understand molecular mechanism DOX-induced search for new therapeutic targets do not sacrifice their anticancer effects. Mitochondria are considered be main target DOX. The imbalance mitochondrial dynamics characterized increased fission inhibited fusion often reported in result excessive ROS production, energy metabolism disorders, cell apoptosis, various other problems. Also, disorder related tumorigenesis. Surprisingly, recent studies show targeting proteins such as DRP1 MFN2 only defend against but also enhance or impair effect. Herein, we summarize cardiac injury. Furthermore, provide overview current pharmacological non-pharmacological interventions involved alleviate damage
Language: Английский
Citations
18Biomedicines, Journal Year: 2023, Volume and Issue: 11(5), P. 1500 - 1500
Published: May 22, 2023
Mitochondria are the main site of intracellular synthesis ATP, which provides energy for various physiological activities cell. Cardiomyocytes have a high density mitochondria and mitochondrial damage is present in variety cardiovascular diseases. In this paper, we describe cardiomyopathy, congenital heart disease, coronary myocardial ischemia-reperfusion injury, failure, drug-induced cardiotoxicity, context key roles cardiac development homeostasis. Finally, discuss current therapeutic strategies aimed at alleviating impairment-related dysfunction, including pharmacological strategies, gene therapy, replacement transplantation. It hoped that will provide new ideas treatment
Language: Английский
Citations
17Small, Journal Year: 2024, Volume and Issue: 20(30)
Published: March 3, 2024
Abstract Doxorubicin (DOX) is widely used as a chemotherapeutic agent for both hematologic and solid tumors reasonable candidate glioma treatment. However, its effectiveness hindered by significant toxicity drug resistance. Moreover, the presence of blood–brain barrier (BBB) brings crucial challenge to therapy. In response, GSH‐responsive actively targeted nanoprodrug delivery system (cRGD/PSDOX‐Cur@NPs) are developed. this system, disulfide bond‐bridged DOX prodrug (PEG‐SS‐DOX) designed release specifically in high glutathione (GSH) tumor environment, markedly reducing cardiotoxicity associated with DOX. To further address resistance, curcumin, serving P‐glycoprotein (P‐gp) inhibitor, effectively increased cellular concentration. Consequently, cRGD/PSDOX‐Cur@NPs exhibited synergistic anti‐tumor effects vitro. Furthermore, vivo experiments validated superior BBB penetration brain‐targeting abilities cRGD/PSDOX‐Cur@NPs, showcasing remarkable potential treating subcutaneous orthotopic gliomas. This research underscores that presents novel approach inhibiting while addressing resistance systemic toxicity.
Language: Английский
Citations
8International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 275, P. 133424 - 133424
Published: June 28, 2024
Language: Английский
Citations
8Free Radical Biology and Medicine, Journal Year: 2024, Volume and Issue: 223, P. 224 - 236
Published: Aug. 6, 2024
Language: Английский
Citations
8