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Tyrosine Kinase Inhibitor Induced Proteinuria - A Review. | LitMetric

Tyrosine Kinase Inhibitor Induced Proteinuria - A Review.

Drug Res (Stuttg)

Department of Medical Oncology, Amrita Health Science Campus, Amrita Vishwa Vidyapeetham, Ponekkara, Kochi, India.

Published: October 2024

AI Article Synopsis

  • Tyrosine Kinase Inhibitors (TKIs) are drugs that disrupt protein kinases' signaling pathways, crucial for tumor cell growth and proliferation, and are commonly used to treat various cancers like colon, breast, kidney, and lung.
  • These inhibitors can be utilized alone or alongside other targeted therapies for better treatment outcomes.
  • However, TKIs may lead to proteinuria in some patients due to issues like dysfunction of the split diaphragm and acute tubular necrosis, which the paper reviews in terms of TKI action mechanisms, associated risks, and management strategies.

Article Abstract

Tyrosine Kinase inhibitor (TKI) is a class of drugs that interfere with protein kinases' signal transduction pathways through an array of inhibitory mechanisms. Tyrosine kinases (TK) have an inevitable role in downstream signal transduction and the proliferation of tumour cells. Hence, tyrosine kinase inhibitors (TKIs) are frequently employed as anti-neoplastic agents in the treatment of colon, breast, kidney, and lung cancers. They can be used as single or combination therapy with other targeted therapies. It is understood that TKIs pose a risk of developing proteinuria in some patients as it can primarily result in dysfunction of the split diaphragm, constriction or blockage of capillary lumens mediated by the basement membrane, acute interstitial nephritis, or acute tubular necrosis. This paper reviews the mechanism of action of TKIs, the pathophysiological mechanism of TKI-induced proteinuria, and its management Fig. 1.

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Source
http://dx.doi.org/10.1055/a-2423-3533DOI Listing

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