Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer

Abstract Cardiotoxic manifestation associated with breast cancer treatment by anthracycline regimen increases patients’ susceptibility to myocardial injury, reduction in left ventricular ejection fraction and complications associated with heart failure. There is currently no standardized, minimally...

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Autores principales: Hari Vishal Lakhani, Sneha S. Pillai, Mishghan Zehra, Benjamin Dao, Maria Tria Tirona, Ellen Thompson, Komal Sodhi
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/43f4b838effc46a2b3b54fd017e269af
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spelling oai:doaj.org-article:43f4b838effc46a2b3b54fd017e269af2021-12-02T14:26:20ZDetecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer10.1038/s41598-021-87209-82045-2322https://doaj.org/article/43f4b838effc46a2b3b54fd017e269af2021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-87209-8https://doaj.org/toc/2045-2322Abstract Cardiotoxic manifestation associated with breast cancer treatment by anthracycline regimen increases patients’ susceptibility to myocardial injury, reduction in left ventricular ejection fraction and complications associated with heart failure. There is currently no standardized, minimally invasive, cost effective and clinically verified procedure to monitor cardiotoxicity post-anthracycline therapy initiation, and to detect early onset of irreversible cardiovascular complications. This study aims to create a panel of novel biomarkers and circulating miRNAs associated with cardiotoxicity, further assessing their correlation with cardiac injury specific markers, troponin I and T, and demonstrate the development of cardiac dysfunction in breast cancer patients. Blood obtained from West Virginian females clinically diagnosed with breast cancer and receiving anthracyclines showed upregulated level of biomarkers and circulating miRNAs after 3 and 6 months of chemotherapy initiation with increased levels of cardiac troponin I and T. These biomarkers and miRNAs significantly correlated with elevated troponins. Following 6 months of anthracycline-regimens, 23% of the patient population showed cardiotoxicity with reduced left ventricular ejection fraction. Our results support the clinical application of plasma biomarkers and circulating miRNAs to develop a panel for early diagnosis of chemotherapy related cardiac dysfunction which will enable early detection of disease progression and management of irreversible cardiac damage.Hari Vishal LakhaniSneha S. PillaiMishghan ZehraBenjamin DaoMaria Tria TironaEllen ThompsonKomal SodhiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hari Vishal Lakhani
Sneha S. Pillai
Mishghan Zehra
Benjamin Dao
Maria Tria Tirona
Ellen Thompson
Komal Sodhi
Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer
description Abstract Cardiotoxic manifestation associated with breast cancer treatment by anthracycline regimen increases patients’ susceptibility to myocardial injury, reduction in left ventricular ejection fraction and complications associated with heart failure. There is currently no standardized, minimally invasive, cost effective and clinically verified procedure to monitor cardiotoxicity post-anthracycline therapy initiation, and to detect early onset of irreversible cardiovascular complications. This study aims to create a panel of novel biomarkers and circulating miRNAs associated with cardiotoxicity, further assessing their correlation with cardiac injury specific markers, troponin I and T, and demonstrate the development of cardiac dysfunction in breast cancer patients. Blood obtained from West Virginian females clinically diagnosed with breast cancer and receiving anthracyclines showed upregulated level of biomarkers and circulating miRNAs after 3 and 6 months of chemotherapy initiation with increased levels of cardiac troponin I and T. These biomarkers and miRNAs significantly correlated with elevated troponins. Following 6 months of anthracycline-regimens, 23% of the patient population showed cardiotoxicity with reduced left ventricular ejection fraction. Our results support the clinical application of plasma biomarkers and circulating miRNAs to develop a panel for early diagnosis of chemotherapy related cardiac dysfunction which will enable early detection of disease progression and management of irreversible cardiac damage.
format article
author Hari Vishal Lakhani
Sneha S. Pillai
Mishghan Zehra
Benjamin Dao
Maria Tria Tirona
Ellen Thompson
Komal Sodhi
author_facet Hari Vishal Lakhani
Sneha S. Pillai
Mishghan Zehra
Benjamin Dao
Maria Tria Tirona
Ellen Thompson
Komal Sodhi
author_sort Hari Vishal Lakhani
title Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer
title_short Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer
title_full Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer
title_fullStr Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer
title_full_unstemmed Detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in West-Virginian population with breast cancer
title_sort detecting early onset of anthracyclines-induced cardiotoxicity using a novel panel of biomarkers in west-virginian population with breast cancer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/43f4b838effc46a2b3b54fd017e269af
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