Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy

被引:34
作者
Jones, Trace M. [1 ,2 ]
Carew, Jennifer S. [1 ,2 ]
Nawrocki, Steffan T. [1 ,2 ]
机构
[1] Dept Med, Div Translat & Regenerat Med, Tucson, AZ 85724 USA
[2] Univ Arizona, Canc Ctr, Tucson, AZ 85724 USA
关键词
renal cell carcinoma; autophagy; hydroxychloroquine; chloroquine; ROC-325; INTERFERON ALPHA-2A; DOUBLE-BLIND; INHIBITOR; CANCER; SURVIVAL; EVEROLIMUS; LYSOSOMES; APOPTOSIS; PHOSPHORYLATION; INTERLEUKIN-2;
D O I
10.3390/cancers12051185
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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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页数:16
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