P20

Targeting KMT9 to reprogramme immune cells in the tumour immune microenvironment in prostate cancer

Project Summary

In P20N, we plan to uncover KMT9-dependent immune escape mechanisms in prostate cancer. We will investigate whether KMT9 inhibitors alone or with CXCR2 inhibitors reprogram immune cells and block tumour growth in Pten/Trp53-KO prostates. Moreover, we will explore whether KMT9 loss enhances anti-PD-1-based immunotherapy (Aim 1). We will also investigate whether KMT9 controls immune cell populations in Pten and Pten/Smad4-KO prostates (Aim 2). In addition, we plan to identify the kinase-dependent signalling mechanism regulating translocation of KMT9 to the nucleus during prostate tumourigenesis (Aim 3)

  • 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