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Updated: Jun 9, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Epigenetics of renal cell carcinoma: the path towards new diagnostics and therapeutics
Mark R Morris1, Eamonn R Maher
1Renal Molecular Oncology Group, Medical and Molecular Genetics, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK. m.r.morris@bham.ac.uk.
Abstract:
Aberrant DNA methylation, in particular promoter hypermethylation and transcriptional silencing of tumor suppressor genes, has an important role in the development of many human cancers, including renal cell carcinoma (RCC). Indeed, apart from mutations in the well studied von Hippel-Lindau gene (VHL), the mutation frequency rates of known tumor suppressor genes in RCC are generally low, but the number of genes found to show frequent inactivation by promoter methylation in RCC continues to grow. Here, we review the genes identified as epigenetically silenced in RCC and their relationship to pathways of tumor development. Increased understanding of RCC epigenetics provides new insights into the molecular pathogenesis of RCC and opportunities for developing novel strategies for the diagnosis, prognosis and management of RCC.
Insights
Aberrant DNA methylation silences tumor suppressor genes in renal cell carcinoma (RCC). This review explores epigenetically silenced genes in RCC, offering new diagnostic and therapeutic strategies.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Aberrant DNA methylation, specifically promoter hypermethylation, leads to tumor suppressor gene silencing and is implicated in human cancers.
- Renal cell carcinoma (RCC) development involves epigenetic alterations, with increasing identification of silenced genes beyond mutations in known genes like VHL.
- Understanding the epigenetic landscape of RCC is crucial for deciphering its molecular pathogenesis.
Purpose of the Study:
- To review genes epigenetically silenced in renal cell carcinoma (RCC).
- To examine the relationship between these silenced genes and tumor development pathways.
- To highlight the potential of epigenetic insights for novel RCC diagnostic, prognostic, and management strategies.
Main Methods:
- Literature review of genes identified as epigenetically silenced in RCC.
- Analysis of the role of these genes in tumor development pathways.
- Synthesis of current understanding of RCC epigenetics.
Main Results:
- A growing number of genes are found to be inactivated by promoter methylation in RCC.
- Epigenetic silencing contributes significantly to RCC pathogenesis, complementing genetic mutations.
- Specific pathways involved in RCC development are linked to these epigenetically silenced genes.
Conclusions:
- Epigenetic silencing of tumor suppressor genes is a key mechanism in RCC development.
- Further understanding of RCC epigenetics provides novel avenues for clinical applications.
- Targeting epigenetic modifications may offer new therapeutic strategies for renal cell carcinoma.
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