2020
DOI: 10.1016/j.biopha.2020.110709
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microRNAs associated to anthracycline-induced cardiotoxicity in women with breast cancer: A systematic review and pathway analysis

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Cited by 28 publications
(22 citation statements)
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“…Upregulation of let-7a can predict the occurrence of cardiotoxicity ( 102 ). The downregulation of the expression of let-7f, a family member of let-7, signified the appearance of cardiac dysfunction because of its good correlation with N-terminal pro-B type natriuretic peptide (NT-proBNP) ( 98 , 103 ). In addition to the let-7 family, miR-1 is another important biomarker, and has also been used as a clinical indicator.…”
Section: Mirnas and Membrane Transportmentioning
confidence: 99%
“…Upregulation of let-7a can predict the occurrence of cardiotoxicity ( 102 ). The downregulation of the expression of let-7f, a family member of let-7, signified the appearance of cardiac dysfunction because of its good correlation with N-terminal pro-B type natriuretic peptide (NT-proBNP) ( 98 , 103 ). In addition to the let-7 family, miR-1 is another important biomarker, and has also been used as a clinical indicator.…”
Section: Mirnas and Membrane Transportmentioning
confidence: 99%
“…miRNAs in serum can be easily obtained and detected using miRNA sequencing methods ( 10 , 75 , 76 ). Therefore, miRNAs have been investigated as non-invasive biomarkers for the early diagnosis of DIC ( 77 ). Table 2 summarizes the clinical significance of miRNAs and their potential roles in DIC.…”
Section: Mirnas For the Diagnosis And Prognosis Of Doxorubicin-induced Cardiomyopathymentioning
confidence: 99%
“…Most myomiRs are expressed both in heart and skeletal muscle: miR-1, miR-133a, miR-133b, miR-486, and miR-499 [56], while some are only expressed in one muscle tissue: cardiospecific miR-208a and skeletal muscle-specific miR-206 [57]. Evidence illustrates that the dysregulation of myomiRs, along with metabolism-related miRNAs, was correlated to adverse cardiac remodelling and toxicity in both preclinical and clinical studies (for review, see Pellegrini et al [22], Pereira et al [58], and Riggeri et al [59]). In neonatal cardiac rat models, the doxorubicin-induced upregulation of miR-146a facilitated cell death in myocytes by targeting ErbB4 and therefore caused cardiotoxicity [60].…”
Section: Cardiorespiratory Toxicitymentioning
confidence: 99%
“…A systematic review for breast cancer patients suggested that let-7, miR-20a, and miR-210 may serve as biomarkers for anthracycline-based cardiotoxicity during chemotherapy [58]. In the rat model treated with doxorubicin at increasing doses, the level of cTnT was significantly elevated in the 18mg/kg dose.…”
Section: Othersmentioning
confidence: 99%