Research Project
Grant-in-Aid for Research Activity Start-up
(1) JNK-mTORC1 pathway is activated in intestinal tumors developed in ApcD716 mutant mice. Experiments using intestinal organoid culture established from wild-type and ApcD716 mutant mice suggest that the JNK-mTORC1 pathway is activated by extracellular signals, rather than via cell autonomous mechanisms.(2) cis-ApcD716/Smad4 compound mutant mice develop tumors that show local invasion. Changes in the composition of intestinal microbiota by antibiotics administration affected colorectal tumorigenesis in cis-ApcD716/Smad4 mutant mice.