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1.
J Cardiovasc Pharmacol Ther ; 23(5): 387-398, 2018 09.
Article in English | MEDLINE | ID: mdl-29706106

ABSTRACT

Pazopanib is an approved treatment for renal cell carcinoma and a second-line treatment for nonadipocytic soft-tissue sarcoma. However, its clinical efficacy is limited by its cardiovascular side effects. Pazopanib and other vascular endothelial growth factor receptor tyrosine kinase inhibitors have been associated with the development of hypertension, QT interval prolongation, and other cardiovascular events; however, these mechanisms are largely unknown. Gaining a deeper understanding of these mechanisms is essential for the development of appropriate surveillance strategies and possible diagnostic biomarkers to allow us to monitor patients and modulate therapy prior to significant cardiac insult. This approach will be vital in keeping patients on these life-saving therapies and may be applicable to other tyrosine kinase inhibitors as well. In this review, we provide a comprehensive overview of the preclinical and clinical side effects of pazopanib with a focus on the mechanisms responsible for its toxicity to the cardiovascular system.


Subject(s)
Angiogenesis Inhibitors/adverse effects , Carcinoma, Renal Cell/drug therapy , Cardiovascular Diseases/chemically induced , Cardiovascular System/drug effects , Kidney Neoplasms/drug therapy , Pyrimidines/adverse effects , Sarcoma/drug therapy , Soft Tissue Neoplasms/drug therapy , Sulfonamides/adverse effects , Angiogenesis Inhibitors/pharmacokinetics , Animals , Carcinoma, Renal Cell/pathology , Cardiovascular Diseases/diagnosis , Cardiovascular Diseases/physiopathology , Cardiovascular System/physiopathology , Humans , Indazoles , Kidney Neoplasms/pathology , Pyrimidines/pharmacokinetics , Risk Assessment , Risk Factors , Sarcoma/pathology , Soft Tissue Neoplasms/pathology , Sulfonamides/pharmacokinetics , Treatment Outcome
2.
Life Sci ; 192: 278-285, 2018 Jan 01.
Article in English | MEDLINE | ID: mdl-29128512

ABSTRACT

Spectrins are large, flexible proteins comprised of α-ß dimers that are connected head-to-head to form the canonical heterotetrameric spectrin structure. Spectrins were initially believed to be exclusively found in human erythrocytic membrane and are highly conserved among different species. ßII spectrin, the most common isoform of non-erythrocytic spectrin, is found in all nucleated cells and forms larger macromolecular complexes with ankyrins and actins. Not only is ßII spectrin a central cytoskeletal scaffolding protein involved in preserving cell structure but it has also emerged as a critical protein required for distinct physiologic functions such as posttranslational localization of crucial membrane proteins and signal transduction. In the heart, ßII spectrin plays a vital role in maintaining normal cardiac membrane excitability and proper cardiac development during embryogenesis. Mutations in ßII spectrin genes have been strongly linked with the development of serious cardiac disorders such as congenital arrhythmias, heart failure, and possibly sudden cardiac death. This review focuses on our current knowledge of the role ßII spectrin plays in the cardiovascular system in health and disease and the potential future clinical implications.


Subject(s)
Heart Diseases/genetics , Heart Diseases/physiopathology , Heart/physiology , Spectrin/genetics , Spectrin/physiology , Animals , Heart/embryology , Heart Diseases/metabolism , Humans
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