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Updated: May 17, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Metabolism of kidney cancer: from the lab to clinical practice
Sunil Sudarshan1, Jose A Karam, James Brugarolas
1Department of Urology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. sudarshan@uab.edu
Context:
There is increasing evidence for the role of altered metabolism in the pathogenesis of renal cancer.
Objective:
This review characterizes the metabolic effects of genes and signaling pathways commonly implicated in renal cancer.
Evidence Acquisition:
A systematic review of the literature was performed using PubMed. The search strategy included the following terms: renal cancer, metabolism, HIF, VHL.
Evidence Synthesis:
Significant progress has been made in the understanding of the metabolic derangements present in renal cancer. These findings have been derived through translational, in vitro, and in vivo studies. To date, the most well-characterized metabolic features of renal cancer are linked to von Hippel-Lindau (VHL) loss. VHL loss and the ensuing increase in the expression of hypoxia-inducible factor affect several metabolic pathways, including glycolysis and oxidative phosphorylation. Collectively, these changes promote a glycolytic metabolic phenotype in renal cancer. In addition, other histologic subtypes of renal cancer are also notable for metabolic derangements that are directly related to the causative genes.
Conclusions:
Current knowledge of the genetics of renal cancer has led to significant understanding of the metabolism of this malignancy. Further studies of the metabolic basis of renal cell carcinoma should provide the foundation for the development of new treatment approaches and development of novel biomarkers.
Insights
Altered metabolism drives renal cancer development. Understanding these metabolic changes, particularly those linked to von Hippel-Lindau (VHL) loss and hypoxia-inducible factor (HIF), is key to new treatments.
Area of Science:
- Oncology
- Molecular Biology
- Metabolic Research
Background:
- Growing evidence links metabolic alterations to renal cancer pathogenesis.
- Understanding these metabolic shifts is crucial for comprehending kidney cancer development.
Purpose of the Study:
- To review the metabolic impacts of genes and signaling pathways frequently involved in renal cancer.
- To synthesize current knowledge on renal cancer metabolism.
Main Methods:
- Systematic literature review using PubMed.
- Search terms included: renal cancer, metabolism, HIF, VHL.
Main Results:
- Renal cancer metabolism is increasingly understood through translational, in vitro, and in vivo studies.
- Von Hippel-Lindau (VHL) loss is a key driver, increasing hypoxia-inducible factor (HIF) and promoting a glycolytic phenotype.
- Metabolic derangements are also observed in other renal cancer subtypes, linked to causative genes.
Conclusions:
- Genetic insights into renal cancer have significantly advanced our understanding of its metabolism.
- Further research into the metabolic basis of renal cell carcinoma can inform novel therapies and biomarkers.
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