Description
The X-linked inhibitor of apoptosis (XIAP) is a member of a family of endogenous caspase inhibitors that act as antiapoptotic factors. XIAP is the most potent caspase inhibitor, blocking both intrinsic and extrinsic apoptotic signals through direct caspase binding. Due to its prominent ability to control cell death and elevated expression in human cancers, XIAP has become an attractive therapeutic target for novel anti-cancer treatment. Small-molecule inhibitors are in various stages of development, from preclinical to phase II clinical trials.
XIAP has an important role in both ovarian cancer as well as in thyroid cancer. This project will explore the efficacy of inhibiting XIAP in combination with targeting a key nuclear receptor in both cancers using unique in vitro systems with innovative technology, novel therapeutic compounds with the ultimate goal of providing an essential pre-clinical, proof of concept approach for translation to the clinic.
Essential criteria:
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords
Cancer; Ovarian Cancer; Thyroid Cancer; Granulosa Cell Tumour; Therapeutics; signalling pathways; transcription factors; nuclear receptors; estrogen; XIAP; apoptosis
School
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research » Molecular and Translational Sciences
Available options
PhD/Doctorate
Honours
BMedSc(Hons)
Time commitment
Full-time
Part-time
Top-up scholarship funding available
No
Physical location
Monash Health Translation Precinct (Monash Medical Centre)
Research webpage
Co-supervisors
Prof
Peter Fuller
Dr
Michael Mond