Metabolic reprogramming in clear cell renal cell carcinoma

被引:362
|
作者
Wettersten, Hiromi I. [1 ]
Abu Aboud, Omran [2 ]
Lara, Primo N., Jr. [3 ]
Weiss, Robert H. [2 ]
机构
[1] Univ Calif San Diego, Sanford Consortium Regenerat Med, Room 4810,2880 Torrey Pines Scen Dr, La Jolla, CA 92037 USA
[2] Univ Calif Davis, Div Nephrol, Genome & Biomed Sci Facil, Room 6311,451 Hlth Sci Dr, Davis, CA 95616 USA
[3] Univ Calif Davis, Comprehens Canc Ctr, 4501 X St,Suite 3003, Sacramento, CA 95817 USA
关键词
POSITRON-EMISSION-TOMOGRAPHY; TUMOR-SUPPRESSOR LKB1; FATTY-ACID SYNTHASE; KIDNEY CANCER; ARGININOSUCCINATE SYNTHETASE; GLUTAMINE-METABOLISM; ARGININE DEPRIVATION; FDG-PET/CT; INDOLEAMINE 2,3-DIOXYGENASE; P53-INDUCIBLE REGULATOR;
D O I
10.1038/nrneph.2017.59
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Research in many cancers has uncovered changes in metabolic pathways that control tumour energetics and biosynthesis, so-called metabolic reprogramming. Studies in clear cell renal cell carcinoma (ccRCC) have been particularly revealing, leading to the concept that ccRCC is a metabolic disease. ccRCC is generally accompanied by reprogramming of glucose and fatty acid metabolism and of the tricarboxylic acid cycle. Metabolism of tryptophan, arginine and glutamine is also reprogrammed in many ccRCCs, and these changes provide opportunities for new therapeutic strategies, biomarkers and imaging modalities. In particular, metabolic reprogramming facilitates the identification of novel and repurposed drugs that could potentially be used to treat ccRCC, which when metastatic has currently limited long-term treatment options. Further research and dissemination of these concepts to nephrologists and oncologists will lead to clinical trials of therapeutics specifically targeted to tumour metabolism, rather than generally toxic to all proliferating cells. Such novel agents are highly likely to be more effective and to have far fewer adverse effects than existing drugs.
引用
收藏
页码:410 / 419
页数:10
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