Efecto sobre el endotelio linfático de la hipoxia tumoral e inhibición de la producción de vegf por flavonoides

  1. Ansó Monclús, Elena
unter der Leitung von:
  1. Juan José Martínez de Irujo Doktorvater

Universität der Verteidigung: Universidad de Navarra

Fecha de defensa: 19 von Dezember von 2008

Gericht:
  1. María Jesús López Zabalza Präsidentin
  2. María Josefa Pajares Villandiego Sekretär/in
  3. María Mercedes Garayoa Berrueta Vocal
  4. Maria Isabel Marzo Rubio Vocal
  5. Ignacio José Encio Martínez Vocal
Fachbereiche:
  1. (FC) Bioquímica y Genética

Art: Dissertation

Teseo: 107391 DIALNET

Zusammenfassung

Vascular endothelial growth factor (VEGF) is an important angiogenic and lymphangiogenic factor highly stimulated by hypoxia. We studied the effect of conditioned media obtained from H157 tumoral lung cancer cells incubated under normoxia (21% O2) or hypoxia (1% O2) on lymphatic endothelial cells (LECs). Gene expression was highly repressed in treated LECs and those related to cell adhesion and angiogenesis were highly perturbed. Functional assays concluded that hypoxic H157 conditioned medium induced LEC proliferation, and cellular adhesion to collagens I and IV, but not to laminin or fibronectin. However, conditioned media did not affect to the adhesion tumoral cells to LECs. On the other hand, we studied the effect of flavonoids on the production of VEGF stimulated by hypoxia. Fisetin, apigenin and luteolin were the most active compounds and hydroxyl substitutions at 3, 5, 7 and 4¿ were important for inhibition of VEGF production under hypoxic conditions. Moreover, our data showed that apoptotic flavonoids induced te phosphorylation of ERK 1/2. Finally, we demonstrated that the mechanism of action of these compounds involved a transcriptional regulation of VEGF gene that were independent of HIF- á expression.