Experimental Oncology Group

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Research Scientists

  • Sara García
  • Carmen Guerra

Post-Doctoral Fellows

  • Juan Carlos López

Graduate Students

  • Domingo Acosta
  • Gonzalo María Aizpurua
  • Oksana Brehey
  • Laura De la Puente
  • Sara Barrambana
  • Ana María Fernández
  • Ana Galván
  • Lucía Lomba
  • Blanca Rosas
  • Pian Sun
  • Elena Zamorano

Technicians

  • Rebeca Barrero
  • Mª Carmen González
  • Silvia Jiménez
  • Alejandra López
  • Marta San Román
  • Raquel Villar

Visiting Scientist

  • Matthias Drosten
  • Mónica Andrea Musteanu

The main thrust of our laboratory is to identify therapeutic strategies against KRAS mutant lung and pancreatic tumours using genetically engineered mouse strains. We recently reported that ablation of KRAS oncogenes induces complete tumour regressions with no signs of tumour resistance. Unfortunately, KRAS inhibitors, either specific for selected mutations or panKRAS inhibitors, only result in partial tumour regressions. Moreover, this limited therapeutic activity is thwarted by the rapid appearance of tumour resistance. Five years ago, we reported that concomitant ablation of two targets involved in KRAS signalling, RAF1 and EGFR, led to the complete disappearance of a limited number of small pancreatic tumours. Yet, most tumours, especially those exhibiting sizes larger than 100 mm3, did not respond to this therapy. We have now identified a third target, STAT3, whose combined ablation with RAF1 and EGFR led to the complete disappearance of all pancreatic tumours regardless of size. More importantly, these mice remained tumour free for up a year. We are now trying to validate this therapeutic strategy using pharmacological approaches with the ultimate goal of translating these results to a clinical scenario.

Recent publications

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