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Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy

Kidney cancer is the 7th most prevalent form of cancer in the United States with the vast majority of cases being classified as renal cell carcinoma (RCC). Multiple targeted therapies have been developed to treat RCC, but efficacy and resistance remain a challenge. In recent years, the modulation of...

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Detalles Bibliográficos
Autores principales: Jones, Trace M., Carew, Jennifer S., Nawrocki, Steffan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281213/
https://www.ncbi.nlm.nih.gov/pubmed/32392870
http://dx.doi.org/10.3390/cancers12051185
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author Jones, Trace M.
Carew, Jennifer S.
Nawrocki, Steffan T.
author_facet Jones, Trace M.
Carew, Jennifer S.
Nawrocki, Steffan T.
author_sort Jones, Trace M.
collection PubMed
description Kidney cancer is the 7th most prevalent form of cancer in the United States with the vast majority of cases being classified as renal cell carcinoma (RCC). Multiple targeted therapies have been developed to treat RCC, but efficacy and resistance remain a challenge. In recent years, the modulation of autophagy has been shown to augment the cytotoxicity of approved RCC therapeutics and overcome drug resistance. Inhibition of autophagy blocks a key nutrient recycling process that cancer cells utilize for cell survival following periods of stress including chemotherapeutic treatment. Classic autophagy inhibitors such as chloroquine and hydroxychloroquine have been introduced into phase I/II clinical trials, while more experimental compounds are moving forward in preclinical development. Here we examine the current state and future directions of targeting autophagy to improve the efficacy of RCC therapeutics.
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spelling pubmed-72812132020-06-15 Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy Jones, Trace M. Carew, Jennifer S. Nawrocki, Steffan T. Cancers (Basel) Review Kidney cancer is the 7th most prevalent form of cancer in the United States with the vast majority of cases being classified as renal cell carcinoma (RCC). Multiple targeted therapies have been developed to treat RCC, but efficacy and resistance remain a challenge. In recent years, the modulation of autophagy has been shown to augment the cytotoxicity of approved RCC therapeutics and overcome drug resistance. Inhibition of autophagy blocks a key nutrient recycling process that cancer cells utilize for cell survival following periods of stress including chemotherapeutic treatment. Classic autophagy inhibitors such as chloroquine and hydroxychloroquine have been introduced into phase I/II clinical trials, while more experimental compounds are moving forward in preclinical development. Here we examine the current state and future directions of targeting autophagy to improve the efficacy of RCC therapeutics. MDPI 2020-05-07 /pmc/articles/PMC7281213/ /pubmed/32392870 http://dx.doi.org/10.3390/cancers12051185 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jones, Trace M.
Carew, Jennifer S.
Nawrocki, Steffan T.
Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy
title Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy
title_full Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy
title_fullStr Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy
title_full_unstemmed Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy
title_short Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy
title_sort therapeutic targeting of autophagy for renal cell carcinoma therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281213/
https://www.ncbi.nlm.nih.gov/pubmed/32392870
http://dx.doi.org/10.3390/cancers12051185
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