Cellular model systems to study cardiovascular injury from chemotherapy.
Hananeh FonoudiMaged M CostantinePublished in: Journal of thrombosis and thrombolysis (2020)
In spite of all the efforts for generating efficient pharmacological treatment options for cancer patients, the unwanted side effect of these substances on the cardiovascular system is becoming a major issue for cancer survivors. The fast pacing oncology field necessitate the quest for more accurate and reliable preclinical screenings. hiPSCs derived cardiomyocytes, endothelial and vascular smooth muscle cells provide unlimited source of physiologically relevant cells that could be used in the screening platforms. Cells derived from hiPSCs can measure drug induced alterations to different aspect of the heart including electrophysiology, contractility and structure. In this review, we will give an overview of the different in vivo and in vitro preclinical drug safety screenings. In following sections, we will focus on hiPSCs derived cardiomyocytes, endothelial and vascular smooth muscle cells and present the current knowledge of the application of these cells in unicellular cardiotoxicity assays. In the final part, we will focus on cardiac organoids as multi cell type platform and their role in cardiotoxicity screening of the chemotherapeutic drugs.
Keyphrases
- vascular smooth muscle cells
- induced apoptosis
- drug induced
- cell cycle arrest
- liver injury
- angiotensin ii
- healthcare
- endoplasmic reticulum stress
- heart failure
- oxidative stress
- squamous cell carcinoma
- endothelial cells
- cell death
- high throughput
- radiation therapy
- left ventricular
- stem cells
- young adults
- signaling pathway
- cell therapy
- mesenchymal stem cells
- drinking water
- atrial fibrillation
- single cell
- bone marrow