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Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy

Renal transplantation (RT) is the best option for patients with end-stage renal disease, but the half-life is limited to a decade due to progressive deterioration of renal function and transplant failure from chronic allograft nephropathy (CAN), which is the leading cause of transplant loss. Extensi...

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Detalles Bibliográficos
Autores principales: Shrestha, Badri Man, Haylor, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058292/
https://www.ncbi.nlm.nih.gov/pubmed/24971332
http://dx.doi.org/10.1155/2014/482438
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author Shrestha, Badri Man
Haylor, John
author_facet Shrestha, Badri Man
Haylor, John
author_sort Shrestha, Badri Man
collection PubMed
description Renal transplantation (RT) is the best option for patients with end-stage renal disease, but the half-life is limited to a decade due to progressive deterioration of renal function and transplant failure from chronic allograft nephropathy (CAN), which is the leading cause of transplant loss. Extensive research has been done to understand the pathogenesis, the biological pathways of fibrogenesis, and potential therapeutic targets for the prevention and treatment of CAN. Despite the advancements in the immunosuppressive agents and patient care, CAN continues to remain an unresolved problem in renal transplantation. The aim of this paper is to undertake a comprehensive review of the literature on the pathogenesis, biological pathways of RT fibrogenesis, and potential therapeutic targets for the prevention and therapy of CAN.
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spelling pubmed-40582922014-06-26 Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy Shrestha, Badri Man Haylor, John Biomed Res Int Review Article Renal transplantation (RT) is the best option for patients with end-stage renal disease, but the half-life is limited to a decade due to progressive deterioration of renal function and transplant failure from chronic allograft nephropathy (CAN), which is the leading cause of transplant loss. Extensive research has been done to understand the pathogenesis, the biological pathways of fibrogenesis, and potential therapeutic targets for the prevention and treatment of CAN. Despite the advancements in the immunosuppressive agents and patient care, CAN continues to remain an unresolved problem in renal transplantation. The aim of this paper is to undertake a comprehensive review of the literature on the pathogenesis, biological pathways of RT fibrogenesis, and potential therapeutic targets for the prevention and therapy of CAN. Hindawi Publishing Corporation 2014 2014-05-27 /pmc/articles/PMC4058292/ /pubmed/24971332 http://dx.doi.org/10.1155/2014/482438 Text en Copyright © 2014 B. M. Shrestha and J. Haylor. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Shrestha, Badri Man
Haylor, John
Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy
title Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy
title_full Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy
title_fullStr Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy
title_full_unstemmed Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy
title_short Biological Pathways and Potential Targets for Prevention and Therapy of Chronic Allograft Nephropathy
title_sort biological pathways and potential targets for prevention and therapy of chronic allograft nephropathy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058292/
https://www.ncbi.nlm.nih.gov/pubmed/24971332
http://dx.doi.org/10.1155/2014/482438
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