Clinical and Translational Oncology

, Volume 12, Issue 1, pp 15–21

Molecular basis for the treatment of renal cell carcinoma

  • Cristina Suárez
  • Rafael Morales
  • Eva Muñoz
  • Jordi Rodón
  • Claudia M. Valverde
  • Joan Carles
Educational Series

DOI: 10.1007/s12094-010-0461-4

Cite this article as:
Suárez, C., Morales, R., Muñoz, E. et al. Clin Transl Oncol (2010) 12: 15. doi:10.1007/s12094-010-0461-4

Abstract

Renal cell carcinoma (RCC) is a heterogeneous malignancy whose incidence rate has notably increased in recent years without any evident reason. Traditionally, RCC has been resistant to classic treatments (chemotherapy, radiotherapy and hormonal therapy), with only a small percentage of patients benefiting from cytokine therapy. Different hereditary syndromes have been associated with RCC, Von Hippel Lindau (VHL) being the most important syndrome. Understanding key molecular pathways implicated in the tumorigenesis of RCC has crystallised in the development of more effective therapies. Specifically, drugs targeting VEGF (bevacizumab, sunitinib, sorafenib, axitinib, pazopanib) and PI3K-mTOR (temsirolimus and everolimus) have become the cornerstone of renal cancer treatment.

Keywords

Renal cell carcinomaMolecular basisTargeted therapiesKey pathways

Copyright information

© Feseo 2010

Authors and Affiliations

  • Cristina Suárez
    • 1
  • Rafael Morales
    • 1
  • Eva Muñoz
    • 1
  • Jordi Rodón
    • 1
  • Claudia M. Valverde
    • 1
  • Joan Carles
    • 1
  1. 1.Department of Medical OncologyVall d’Hebrón University HospitalBarcelonaSpain