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dc.contributor.authorKim, Minkyoung
dc.contributor.supervisorMarco Falascaen_US
dc.date.accessioned2021-07-14T05:39:08Z
dc.date.available2021-07-14T05:39:08Z
dc.date.issued2020en_US
dc.identifier.urihttp://hdl.handle.net/20.500.11937/84527
dc.description.abstract

This PhD thesis discusses the novel therapeutic target of PDAC, which is GPR35. For the first time, we have characterized its diverse roles controlling apoptosis, autophagy, cell cycle arrests, migration and invasion in PDAC cells. In addition, this work provides its related signalling pathways which are AKT and HIF-1. Our investigation of GPR35 in PDAC has contributed to suggest a new therapeutic strategy to cure pancreatic cancer patients.

en_US
dc.publisherCurtin Universityen_US
dc.titleThe role of G protein-coupled receptor 35 in pancreatic canceren_US
dc.typeThesisen_US
dcterms.educationLevelPhDen_US
curtin.departmentCurtin Medical Schoolen_US
curtin.accessStatusOpen accessen_US
curtin.facultyHealth Sciencesen_US


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