P19

Focal adhesion kinase (FAK) dependent immune escape in hepatocellular carcinoma

Project Summary

In P19 we plan to evaluate the role of oncogenic Focal Adhesion Kinase (FAK) signalling as a common and targetable driver of immune escape in Hepatocellular carcinoma (HCC). Using Imaging Mass Cytometry and FAK gain and loss of-function models we will determine the key immune effector components affected by FAK-mediated immune escape (Aim 1). Aim 2 is dedicated to the identification of the driving pathways and mediators of this immune escape. In Aim 3 we will assess the therapeutic potential of targeting FAK for overcoming resistance to immune checkpoint inhibition in HCC.

  • P01Blaeschke / Zeiser
  • P02Greten
  • P03Köhler / Briquez
  • P05Apostolova / Kierdorf
  • P07Prinz
  • P08Frew
  • P10Heikenwälder / Hofmann
  • P12Duyster / Kolter
  • P14Brummer
  • P15Minguet
  • P17Ruess / Bengsch
  • P18Hoefflin / Sevenich
  • P19Hofmann / Röhlen
  • P20Metzger
  • P21Böttcher
  • P22Feuchtinger / Maas-Bauer
  • P23Ingelfinger / Sevenich
  • P24Vinnakota / Wertheimer
  • P25Pahl / Rizzi
  • S1Börries / Köttgen / Schell
  • S2Reichardt / Talvard-Balland
  • INFBinder
  • ZZeiser
  • IRTGBörries
  • P16EErlacher
  • P06EGroß
  • P04EIllert
  • P13ENyström / Kiritsi
  • P05 1.FPCabezas-Wallscheid
  • S01 1.FPSchilling