| Literature DB >> 26860342 |
Anupam Agarwal1, Zheng Dong2, Raymond Harris3, Patrick Murray4, Samir M Parikh5, Mitchell H Rosner6, John A Kellum7, Claudio Ronco8.
Abstract
In this article, we review the current evidence for the cellular and molecular mechanisms of AKI, focusing on epithelial cell pathobiology and related cell-cell interactions, using ischemic AKI as a model. Highlighted are the clinical relevance of cellular and molecular targets that have been investigated in experimental models of ischemic AKI and how such models might be improved to optimize translation into successful clinical trials. In particular, development of more context-specific animal models with greater relevance to human AKI is urgently needed. Comorbidities that could alter patient susceptibility to AKI, such as underlying diabetes, aging, obesity, cancer, and CKD, should also be considered in developing these models. Finally, harmonization between academia and industry for more clinically relevant preclinical testing of potential therapeutic targets and better translational clinical trial design is also needed to achieve the goal of developing effective interventions for AKI.Entities:
Keywords: acute renal failure; kidney; pathophysiology of renal disease and progression
Mesh:
Year: 2016 PMID: 26860342 PMCID: PMC4849836 DOI: 10.1681/ASN.2015070740
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121