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Updated: Jul 10, 2026

Modeling Spontaneous Metastatic Renal Cell Carcinoma (mRCC) in Mice Following Nephrectomy
Published on: April 29, 2014
Sunitinib, sorafenib and mTOR inhibitors in renal cancer
Sinisa Radulovic1, Snezana K Bjelogrlic
1Department of Translational Research, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia. sinisar@ncrc.ac.yu
Abstract:
Understanding the alterations in cellular protein interactions and their relations to genetic mutations that cause renal cell carcinoma (RCC) provides a unique opportunity for the development of disease-specific therapy for patients with advanced forms of this disease. There is substantial evidence of an association between mutation on von Hippel-Lindau (VHL) gene and the earliest stages of tumorigenesis of RCC. The main consequence of VHL loss is the upregulation of downstream proangiogenic factors leading to highly vascular tumors. Overexpression of hypoxia inducible factor (HIF) is also caused by the mammalian target of rapamycin (mTOR), a key component of signaling pathways inside the cell, involved in cell proliferation. The inhibition of proangiogenic factors and mTOR was the main idea behind the development of new targeted agents in advanced RCC. Since December 2005, 3 targeted agents have been approved by the U.S. Food and Drug Administration (FDA) for the treatment of advanced RCC: sorafenib, sunitinib and temsirolimus. Sorafenib and sunitinib are synthetic, orally active agents shown to directly inhibit vascular endothelial growth factor receptors -2 and -3 (VEGFR-2, VEGFR-3) and platelet-derived growth factor receptor beta (PDGFR-beta), while temsirolimus is an mTOR inhibitor. Recent clinical studies form the basis for new guidelines for the treatment of advanced RCC: sorafenib should be used as a second-line treatment, sunitinib as the first-line therapy for good and intermediate-risk patients, and temsirolimus should be considered as first-line treatment for poor-risk patients. Future approaches to targeted therapy should focus on optimizing the use of current active drugs, exploring their combinations or investigating their sequential use. In addition, it is important to define the mechanisms of resistance on their use and to further investigate biomarkers and enhance treatment efficacy for the individual patients. The development of these targeted therapies represents an exciting step forward in the treatment of advanced RCC.
Insights
Targeted therapies like sorafenib, sunitinib, and temsirolimus offer new hope for advanced renal cell carcinoma (RCC) by inhibiting key pathways. Understanding VHL gene mutations and targeted agent mechanisms is crucial for optimizing treatment and overcoming resistance.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Renal cell carcinoma (RCC) tumorigenesis is linked to von Hippel-Lindau (VHL) gene mutations, leading to increased proangiogenic factors and vascular tumors.
- Mammalian target of rapamycin (mTOR) pathway activation, driven by hypoxia-inducible factor (HIF), promotes cell proliferation in RCC.
Purpose of the Study:
- To review the development and current guidelines for targeted agents in advanced RCC treatment.
- To explore future directions in optimizing targeted therapy, including combinations, sequential use, and resistance mechanisms.
Main Methods:
- Review of clinical studies and FDA-approved targeted agents for advanced RCC.
- Analysis of mechanisms of action for sorafenib, sunitinib, and temsirolimus.
- Examination of current treatment guidelines based on patient risk stratification.
Main Results:
- Three targeted agents approved: sorafenib and sunitinib (VEGFR/PDGFR inhibitors) and temsirolimus (mTOR inhibitor).
- Established guidelines recommend sunitinib as first-line for good/intermediate-risk, temsirolimus for poor-risk, and sorafenib as second-line therapy.
- Targeted therapies have significantly advanced advanced RCC treatment.
Conclusions:
- Targeted therapies targeting angiogenesis and mTOR pathways represent a significant advancement in treating advanced RCC.
- Future research should focus on optimizing drug combinations, sequential use, understanding resistance, and identifying biomarkers for personalized treatment.
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