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Projekt Druckansicht

Die Rolle des Plazentaren Gens PEG10 im Rahmen der neuroendokrinen Transdifferenzierung des Prostatakarzinoms

Antragsteller Dr. Alexander Kretschmer
Fachliche Zuordnung Reproduktionsmedizin, Urologie
Förderung Förderung von 2015 bis 2017
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 269895856
 
Erstellungsjahr 2018

Zusammenfassung der Projektergebnisse

The project initially termed “The Role Of Placental Gene PEG10 During Transdifferentiation Into Neuroendocrine Prostate Cancer” was modified before the start of my research fellowship, because of the development of the project between the time of my application and the time of the start of the research fellowship. The resulting project was termed “Characterization of stress-induced tunneling nanotubes and their support of treatment adaptation in prostate cancer”. Here, we define roles of tunneling nanotubes (TNTs), a newly identified stress-induced structure for intercellular communication, in stress adaptation and treatment resistance in prostate cancer (PCa). Androgen receptor (AR) blockade and metabolic stress induce TNTs in PCa, but not in normal prostatic epithelial and osteoblast cells. Co-culture assays reveal enhanced TNT formation between stressed and unstressed PCa cells as well as from stressed PCa to osteoblasts. Stress chaperones clusterin (CLU), YB-1 and Hsp27 localize within TNTs, and CLU-containing particles are transported bi-directionally via TNTs. TNT formation was attenuated by PI3K inhibition and also by silencing CLU or YB-1. AR splice variant V7, which is induced by AR antagonism and help mediate resistance to AR pathway inhibition, enhances TNT formation and rescues loss of CLU- or YB-1-repressed TNT formation. Disruption of TNT sensitizes PCa to AR blockade- or metabolic stress-induced cell death. These data identify induction of TNT formation by PCa cells for intercellular communication of stress-associated material to confer survival.

Projektbezogene Publikationen (Auswahl)

 
 

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