Methods for Identifying Risk of Chemotherapy-Induced Cardiotoxicity and Targeted Medical Intervention
AssigneeDetroit R&D, Inc.
InventorHyesook Kim
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AssigneeDetroit R&D, Inc.
InventorHyesook Kim
Estimating the term…
This invention discloses diagnosis of risk of chemotherapy-induced cardiotoxicity by measurement of increased expression of soluble epoxide hydrolase in vitro and in vivo in cells, tissues or animals including measurement of increased levels of soluble epoxide hydrolase metabolites, e.g., 14,15-DHET and 11,12-DHET, in biological fluids. This invention also includes diagnosis of risk of chemotherapy-induced cardiotoxicity by measuring increased levels of oxidative stress in cells, tissues or animals including measurement of increased levels of oxidative stress biomarkers, e.g., 8-isoprostane, in biological fluids. Fatty acid and protein biomarkers to diagnose the risk of chemotherapy-induced cardiotoxicity are detected using various detection methods including mass spectrometry and immunoassay such as ELISA, Western blot analysis or label-free microwell and nanowell technologies. This invention discloses targeted medical intervention for a subject who is at risk or with chemotherapy-induced cardiotoxicity by treating with soluble epoxide hydrolase inhibitor(s) with or without antioxidants to prevent or ameliorate the chemotherapy-induced cardiotoxicity.
A method to identify risk of chemotherapy-induced cardiotoxicity using biomarkers that predict cardiotoxicity by the steps of:
A method to identify sEH-dependent cardiotoxicity after chemotherapy using a metabolite of sEH by the steps of:
Treatment of natural or synthetic soluble epoxide hydrolase inhibitor or a mixture of soluble epoxide hydrolase inhibitors with or without oxidative stress inhibitors to prevent or ameliorate the chemotherapy-induced cardiotoxicity.
A method to measure fatty acids and proteins in biological samples including biological fluids using label-free microwell or nanowell technology by the steps of:
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