Human tumor xenografts are phenocopies of the originating patient cancer and keep their clonal and spatial architecture despite being grown in heavily immunodeficient mice.
I will show some recent and unpublished work from my laboratory that unravels:
These data demonstrate the potential of using human cancer xenografts to characterize the fundamental biology of tumor ecosystems, including how these are initiated and maintained, with obvious implications for the study of dormancy, metastases and therapy resistance.