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Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics

The antineoplastic platinum complexes cisplatin and its analogues are widely used in the chemotherapy of a variety of human malignancies, and are especially active against several types of cancers. Nedaplatin is a second-generation platinum complex with reduced nephrotoxicity. However, their use com...

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Autores principales: Uehara, Takeki, Yamate, Jyoji, Torii, Mikinori, Maruyama, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Toxicologic Pathology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234610/
https://www.ncbi.nlm.nih.gov/pubmed/22272048
http://dx.doi.org/10.1293/tox.24.87
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author Uehara, Takeki
Yamate, Jyoji
Torii, Mikinori
Maruyama, Toshiyuki
author_facet Uehara, Takeki
Yamate, Jyoji
Torii, Mikinori
Maruyama, Toshiyuki
author_sort Uehara, Takeki
collection PubMed
description The antineoplastic platinum complexes cisplatin and its analogues are widely used in the chemotherapy of a variety of human malignancies, and are especially active against several types of cancers. Nedaplatin is a second-generation platinum complex with reduced nephrotoxicity. However, their use commonly causes nephrotoxicity due to a lack of tumor tissue selectivity. Several recent studies have provided significant insights into the molecular and histopathological events associated with nedaplatin nephrotoxicity. In this review, we summarize findings concerning the renal histopathology and molecular pathogenesis induced by antineoplastic platinum complexes, with a particular focus on the comparative nephrotoxicity of cisplatin and nedaplatin in rats.
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spelling pubmed-32346102012-01-23 Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics Uehara, Takeki Yamate, Jyoji Torii, Mikinori Maruyama, Toshiyuki J Toxicol Pathol Review The antineoplastic platinum complexes cisplatin and its analogues are widely used in the chemotherapy of a variety of human malignancies, and are especially active against several types of cancers. Nedaplatin is a second-generation platinum complex with reduced nephrotoxicity. However, their use commonly causes nephrotoxicity due to a lack of tumor tissue selectivity. Several recent studies have provided significant insights into the molecular and histopathological events associated with nedaplatin nephrotoxicity. In this review, we summarize findings concerning the renal histopathology and molecular pathogenesis induced by antineoplastic platinum complexes, with a particular focus on the comparative nephrotoxicity of cisplatin and nedaplatin in rats. The Japanese Society of Toxicologic Pathology 2011-06-30 2011-06 /pmc/articles/PMC3234610/ /pubmed/22272048 http://dx.doi.org/10.1293/tox.24.87 Text en ©2011 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Review
Uehara, Takeki
Yamate, Jyoji
Torii, Mikinori
Maruyama, Toshiyuki
Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics
title Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics
title_full Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics
title_fullStr Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics
title_full_unstemmed Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics
title_short Comparative Nephrotoxicity of Cisplatin and Nedaplatin: Mechanisms and Histopathological Characteristics
title_sort comparative nephrotoxicity of cisplatin and nedaplatin: mechanisms and histopathological characteristics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234610/
https://www.ncbi.nlm.nih.gov/pubmed/22272048
http://dx.doi.org/10.1293/tox.24.87
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