Novel molecular biomarkers of cancer therapy-induced cardiotoxicity in adult population: a scoping review
Primer Autor |
Riffo-Campos, Angela L.
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Co-autores |
Cartas-Espinel, Irene
Telechea-Fernandez, Marcelino
Manterola Delgado, Carlos
Avila Barrera, Andres
Saavedra Cuevas, Nicolas
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Título |
Novel molecular biomarkers of cancer therapy-induced cardiotoxicity in adult population: a scoping review
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Editorial |
WILEY PERIODICALS, INC
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Revista |
ESC HEART FAILURE
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Lenguaje |
en
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Resumen |
Aim Cancer treatments are associated with cardiotoxic events that predispose to cardiac pathology and compromise the survival of patients, making necessary the identification of new molecular biomarkers to detect cardiotoxicity. This scoping review aims to identify the available evidence on novel molecular biomarkers associated with cardiotoxicity in the adult population undergoing cancer therapy. Methods and results The databases Medline, Web of Science, Scopus, and Embase were screened for the identification of published studies until 23 August 2020, searching for novel molecular biomarkers reported in cancer therapy-related cardiac dysfunction in adult patients. A total of 42 studies that met the eligibility criteria were included. Fourteen studies reported 44 new protein biomarkers, 18 studies reported 57 new single nucleotide polymorphism biomarkers, and 11 studies reported 171 new gene expression profiles associated with cardiotoxicity. Data were extracted for 272 novel molecular biomarkers reported and evaluated in 7084 cancer patients, of which only 13 were identified in more than one study (MPO, sST2, GDF-15, TGF-B1, rs1056892, rs1883112, rs4673, rs13058338, rs1695, miR-1, miR-25-3p, miR-34a-5p, and miR-423-5p), showing values for area under the curve > 0.73 (range 0.74-0.85), odds ratio 0.26-7.17, and hazard ratio 1.28-1.80. Conclusions Multiple studies presented a significant number of novel molecular biomarkers as promising predictors for risk assessment of cardiac dysfunction related to cancer therapy, but the characteristics of the studies carried out and the determinations applied do not allow suggesting the clinical use of these molecular biomarkers in the assessment of cancer therapy-induced cardiotoxicity.
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Tipo de Recurso |
artículo de revisión
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Description |
This work was supported by the Chilean ANID/Fondecyt-Postdoctorado No. 3180486 (A.L.R.-C), and Grants ANID/Doctorado Nacional No. 21150650 (I.C.-E.) and supported by the Universidad de La Frontera, project DI22-0014 (A.L.R.-C and I.C.-E.).
Este trabajo fue apoyado por la ANID/Fondecyt-Postdoctorado de Chile No. 3180486 (A.L.R.-C), y Becas ANID/Doctorado Nacional No. 21150650 (I.C.-E.) y apoyado por la Universidad de La Frontera, proyecto DI22-0014 ( A.L.R.-C e I.C.-E.).
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doi |
10.1002/ehf2.13735
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Formato Recurso |
PDF
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Palabras Claves |
Cardiotoxicity
Molecular biomarkers
LVEF
CTRCD
Cancer therapy
Cardio-oncology/onco-cardiology
DOXORUBICIN-INDUCED CARDIOTOXICITY
GENOME-WIDE ASSOCIATION
T-CELL THERAPY
MULTIPLE BIOMARKERS
CARDIAC TOXICITY
HEART-FAILURE
POLYMORPHISM
MANAGEMENT
RISK
HER2
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Ubicación del archivo | |
Categoría OCDE |
Sistemas cardíacos y cardiovasculares
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Materias |
Cardiotoxicidad
Biomarcadores moleculares
FEVI
CTRCD
Terapia contra el cáncer
Cardiooncología/oncocardiología
CARDIOTOXICIDAD INDUCIDA POR DOXORUBICINA
ASOCIACIÓN DE TODO EL GENOMA
TERAPIA DE CÉLULAS T
BIOMARCADORES MÚLTIPLES
TOXICIDAD CARDIACA
INSUFICIENCIA CARDÍACA
POLIMORFISMO
MANEJO
RIESGO
HER2
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Título de la cita (Recomendado-único) |
Novel molecular biomarkers of cancer therapy-induced cardiotoxicity in adult population: a scoping review
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Página de inicio (Recomendado-único) |
1651
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Página final (Recomendado-único) |
1665
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Identificador del recurso (Mandatado-único) |
artículo de revisión
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Versión del recurso (Recomendado-único) |
version publicada
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License |
CC BY-NC 4.0
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Condición de la licencia (Recomendado-repetible) |
CC BY-NC 4.0
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Derechos de acceso |
acceso abierto
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Access Rights |
acceso abierto
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Referencia del Financiador (Mandatado si es aplicable-repetible) |
ANID-FONDECYT 3180486
ANID-FONDECYT 21150650
UFRO DI22-0014
ANID FONDECYT 3180486
ANID FONDECYT 21150650
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Id de Web of Science |
WOS:000766005500001
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