Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies

A significantly increased level of the reactive oxygen species (ROS) scavenger glutathione (GSH) has been identified as a hallmark of renal cell carcinoma (RCC). The proposed mechanism for increased GSH levels is to counteract damaging ROS to sustain the viability and growth of the malignancy. Here,...

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Main Authors: Yi Xiao, David Meierhofer
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/15/3672
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spelling doaj-81b74c9c88bc4bfca5f9d4600e8065a12020-11-25T01:54:18ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-07-012015367210.3390/ijms20153672ijms20153672Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for TherapiesYi Xiao0David Meierhofer1Max Planck Institute for Molecular Genetics, Ihnestraße 63-73, 14195 Berlin, GermanyMax Planck Institute for Molecular Genetics, Ihnestraße 63-73, 14195 Berlin, GermanyA significantly increased level of the reactive oxygen species (ROS) scavenger glutathione (GSH) has been identified as a hallmark of renal cell carcinoma (RCC). The proposed mechanism for increased GSH levels is to counteract damaging ROS to sustain the viability and growth of the malignancy. Here, we review the current knowledge about the three main RCC subtypes, namely clear cell RCC (ccRCC), papillary RCC (pRCC), and chromophobe RCC (chRCC), at the genetic, transcript, protein, and metabolite level and highlight their mutual influence on GSH metabolism. A further discussion addresses the question of how the manipulation of GSH levels can be exploited as a potential treatment strategy for RCC.https://www.mdpi.com/1422-0067/20/15/3672Renal cell carcinoma (RCC)reactive oxygen species (ROS)glutathione (GSH) metabolismcancer therapyclear cell RCCpapillary RCCchromophobe RCC
collection DOAJ
language English
format Article
sources DOAJ
author Yi Xiao
David Meierhofer
spellingShingle Yi Xiao
David Meierhofer
Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies
International Journal of Molecular Sciences
Renal cell carcinoma (RCC)
reactive oxygen species (ROS)
glutathione (GSH) metabolism
cancer therapy
clear cell RCC
papillary RCC
chromophobe RCC
author_facet Yi Xiao
David Meierhofer
author_sort Yi Xiao
title Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies
title_short Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies
title_full Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies
title_fullStr Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies
title_full_unstemmed Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies
title_sort glutathione metabolism in renal cell carcinoma progression and implications for therapies
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-07-01
description A significantly increased level of the reactive oxygen species (ROS) scavenger glutathione (GSH) has been identified as a hallmark of renal cell carcinoma (RCC). The proposed mechanism for increased GSH levels is to counteract damaging ROS to sustain the viability and growth of the malignancy. Here, we review the current knowledge about the three main RCC subtypes, namely clear cell RCC (ccRCC), papillary RCC (pRCC), and chromophobe RCC (chRCC), at the genetic, transcript, protein, and metabolite level and highlight their mutual influence on GSH metabolism. A further discussion addresses the question of how the manipulation of GSH levels can be exploited as a potential treatment strategy for RCC.
topic Renal cell carcinoma (RCC)
reactive oxygen species (ROS)
glutathione (GSH) metabolism
cancer therapy
clear cell RCC
papillary RCC
chromophobe RCC
url https://www.mdpi.com/1422-0067/20/15/3672
work_keys_str_mv AT yixiao glutathionemetabolisminrenalcellcarcinomaprogressionandimplicationsfortherapies
AT davidmeierhofer glutathionemetabolisminrenalcellcarcinomaprogressionandimplicationsfortherapies
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