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Updated: Jun 14, 2026

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
Kinase targets in renal-cell carcinomas: reassessing the old and discovering the new
Kyle A Furge1, Jeffrey P MacKeigan, Bin T Teh
1Laboratory of Computational Biology, Van Andel Research Institute, Grand Rapids, MI, USA.
Abstract:
Renal-cell carcinoma is a heterogeneous group of tumours that arise in the adult kidneys. Irrespective of the type of renal tumour, traditional chemotherapeutic and radiation-based therapies have been largely ineffective at treating advanced tumours, with long-term survival being very low. Molecularly-targeted inhibitors of protein kinases are effective in delaying progression of advanced renal tumours. These therapies revolve around inhibition of the vascular endothelial growth factor receptor tyrosine kinase and the mammalian target of rapamycin serine or threonine kinase signalling pathways. The genetic complexity of renal tumours revealed by gene-expression profiling and other molecular-genetic technologies indicate that inhibition of additional kinase-associated pathways could also prevent renal tumour growth. In this review, we discuss the use of molecularly-targeted kinase inhibitors in the treatment of renal-cell carcinoma and identify the next generation of kinase inhibitors that show promise for treatment.
Insights
Molecularly-targeted kinase inhibitors show promise for treating advanced renal-cell carcinoma (RCC). These therapies target key signaling pathways, offering improved progression delay compared to traditional treatments.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Renal-cell carcinoma (RCC) is a diverse kidney tumor group with poor outcomes from traditional therapies.
- Advanced RCC demonstrates limited response to chemotherapy and radiation, necessitating novel treatment strategies.
- Molecularly-targeted inhibitors have emerged as effective treatments for advanced RCC.
Purpose of the Study:
- To review the current use of molecularly-targeted kinase inhibitors in renal-cell carcinoma treatment.
- To explore the genetic complexity of renal tumors and identify new therapeutic targets.
- To highlight next-generation kinase inhibitors with potential for improved RCC treatment.
Main Methods:
- Review of scientific literature on kinase inhibitors and renal-cell carcinoma.
- Analysis of gene-expression profiling and molecular-genetic data in renal tumors.
- Discussion of targeted therapies focusing on vascular endothelial growth factor receptor (VEGFR) and mammalian target of rapamycin (mTOR) pathways.
Main Results:
- Molecularly-targeted kinase inhibitors, particularly those inhibiting VEGFR and mTOR pathways, are effective in delaying advanced RCC progression.
- Genetic complexity of RCC suggests that targeting additional kinase pathways could further inhibit tumor growth.
- Current targeted therapies offer improved outcomes over traditional treatments for advanced renal tumors.
Conclusions:
- Molecularly-targeted kinase inhibitors represent a significant advancement in managing advanced renal-cell carcinoma.
- Further research into novel kinase targets and inhibitors is crucial for enhancing RCC treatment efficacy.
- The future of RCC treatment lies in personalized therapies that exploit the molecular intricacies of the disease.
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