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Updated: May 11, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
How far is the horizon? From current targets to future drugs in advanced renal cancer
Stephan Kruck1, Axel S Merseburger, Arnulf Stenzl
1Department of Urology, Eberhard-Karls-University Tuebingen, Hoppe-Seyler Strasse 3, 72076, Tuebingen, Germany, Stephan.Kruck@med.uni-tuebingen.de.
Purpose:
The proliferative control of renal cell cancer (RCC) via vascular endothelial growth factor and mammalian target of rapamycin inhibition by targeted agents has substantially improved survival rates for RCC patients with metastatic (m) disease. However, the management of mRCC remains challenging because some patients are primarily refractory to the approved targeted agents and most therapies eventually fail because of the development of an intractable drug resistance. Tumor progression is closely related to a persistent or restored proliferation via direct and indirect oncogenic signals. Although the elucidation of cancer cell proliferation in the "-omics era" has revealed an enormous number of new potential targets, a comprehensive overview of the different pathways that might serve as new drug targets has become increasingly complex.
Methods/Results:
This review highlights the well-trodden pathways in mRCC that are inhibited by targeting agents and describes innovative modes of action within these pathways that are currently not targeted but are under exploration in clinical studies. Additionally, this paper highlights as future drug targets the components of tumor metabolism that supply the tumor cells with nutrition.
Conclusions:
These fundamental insights into RCC proliferation as a key driver of progression are urgently needed to overcome the currently improved but still limited targeted drug success.
Insights
Targeted therapies improve survival for metastatic renal cell cancer (mRCC) but face resistance. New strategies targeting tumor metabolism and novel pathways are crucial for overcoming drug resistance in mRCC.
Area of Science:
- Oncology
- Cancer Biology
Background:
- Metastatic renal cell cancer (mRCC) management improved with targeted agents inhibiting vascular endothelial growth factor and mammalian target of rapamycin.
- Drug resistance and primary refractoriness remain significant challenges in mRCC treatment.
- Tumor progression in mRCC is driven by persistent or restored cancer cell proliferation via oncogenic signaling.
Purpose of the Study:
- To review established targeted pathways in mRCC.
- To explore innovative therapeutic strategies within these pathways currently under clinical investigation.
- To identify tumor metabolism components as potential future drug targets for mRCC.
Main Methods:
- Literature review of targeted agents and pathways in mRCC.
- Analysis of current clinical studies exploring novel therapeutic approaches.
- Identification of emerging targets in tumor metabolism.
Main Results:
- Established targeted agents inhibit key proliferative pathways in mRCC.
- Innovative therapeutic strategies targeting existing pathways are under clinical evaluation.
- Tumor metabolism components are emerging as promising targets for future mRCC therapies.
Conclusions:
- Understanding RCC proliferation is essential for improving targeted drug efficacy.
- Overcoming drug resistance in mRCC requires exploring novel targets and pathways.
- Targeting tumor metabolism offers a promising avenue for future mRCC treatment strategies.
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