miRNA Expression Profiles in Isolated Ventricular Cardiomyocytes: Insights into Doxorubicin-Induced Cardiotoxicity

被引:2
|
作者
Romero, Yohana Dominguez [1 ,2 ]
Ortiz, Gladis Montoya [2 ]
Herran, Susana Novoa [2 ]
Mendez, Jhon Osorio [2 ,3 ]
Grosso, Luis A. Gomez [2 ,4 ]
机构
[1] Univ Nacl Colombia, Fac Sci, Doctorate Biotechnol Program, Bogota 111321, Colombia
[2] Natl Inst Hlth, Mol Physiol Grp, Subdirect Sci & Technol Res, Direct Publ, Bogota 111321, Colombia
[3] Univ Nacl Colombia, Fac Med, Dept Physiol Sci, Master Biochem Program, Bogota 111321, Colombia
[4] Univ Nacl Colombia, Fac Med, Dept Physiol Sci, Bogota 111321, Colombia
关键词
doxorubicin; cardiotoxicity; cardioprotection; miRNAs; KATP; SIRT1; FOXO1; GSK3B; HEART-FAILURE; ELECTROPHYSIOLOGICAL CHANGES; TRANSCRIPTION FACTORS; CELL-DEATH; APOPTOSIS; CYTOSCAPE; CARDIOLIPIN; MECHANISMS; SYNTHASE; ROLES;
D O I
10.3390/ijms25105272
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Doxorubicin (DOX), widely used as a chemotherapeutic agent for various cancers, is limited in its clinical utility by its cardiotoxic effects. Despite its widespread use, the precise mechanisms underlying DOX-induced cardiotoxicity at the cellular and molecular levels remain unclear, hindering the development of preventive and early detection strategies. To characterize the cytotoxic effects of DOX on isolated ventricular cardiomyocytes, focusing on the expression of specific microRNAs (miRNAs) and their molecular targets associated with endogenous cardioprotective mechanisms such as the ATP-sensitive potassium channel (KATP), Sirtuin 1 (SIRT1), FOXO1, and GSK3 beta. We isolated Guinea pig ventricular cardiomyocytes by retrograde perfusion and enzymatic dissociation. We assessed cell morphology, Reactive Oxygen Species (ROS) levels, intracellular calcium, and mitochondrial membrane potential using light microscopy and specific probes. We determined the miRNA expression profile using small RNAseq and validated it using stem-loop qRT-PCR. We quantified mRNA levels of some predicted and validated molecular targets using qRT-PCR and analyzed protein expression using Western blot. Exposure to 10 mu M DOX resulted in cardiomyocyte shortening, increased ROS and intracellular calcium levels, mitochondrial membrane potential depolarization, and changes in specific miRNA expression. Additionally, we observed the differential expression of KATP subunits (ABCC9, KCNJ8, and KCNJ11), FOXO1, SIRT1, and GSK3 beta molecules associated with endogenous cardioprotective mechanisms. Supported by miRNA gene regulatory networks and functional enrichment analysis, these findings suggest that DOX-induced cardiotoxicity disrupts biological processes associated with cardioprotective mechanisms. Further research must clarify their specific molecular changes in DOX-induced cardiac dysfunction and investigate their diagnostic biomarkers and therapeutic potential.
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页数:24
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