Associate Professor Charles de Bock

Associate Professor Charles de Bock

Conjoint Associate Professor

2006            PhD (Cancer Biology), University of New South Wales, Australia
2000            MSc (Medical Science), First Class, University of Auckland, New Zealand
1998            BSc (Pharmacology), University of Auckland, New Zealand
 

Medicine & Health
School of Clinical Medicine

I joined the Institute in January 2019 to establish a new team to work on one of the most difficult to treat blood cancers in children: T-cell acute lymphoblastic leukaemia (T-ALL). A molecular and cellular biologist with over 10 years’ experience researching blood cancers, with a unique skill set combined with a passion to see my research make a difference in people’s lives.

‘Children with T-ALL are high-risk and so receive a very intensive chemotherapy regimen. Many of these children suf...

E-mail
cdebock@ccia.org.au
Location
Lowy Cancer Research Centre, UNSW Australia PO Box 81 Randwick 2031 Australia

2021    Haematology Society Australia and New Zealand (HSANZ)/ Snowdome Mid-career award

2017    True Colours/VIB 4-day leadership program

2017    Technology transfer and the exploitation of research, KU Leuven. Team awarded 1st place for exploitation plan.

2008    New South Wales (NSW) Office of Science and Medical Research Award for Best Postdoctoral Oral Presentation; ASMR NSW Meeting.

2004    St George Hospital Clinical School “Young Investigator of the Year” 

1998    Fowlds Memorial Prize for most distinguished student in the Medicine and Health Science Faculty, University of Auckland, New Zealand

1997    Senior Prize in Pharmacology, University of Auckland, New Zealand
 

Personalised anti-cancer therapies have the potential to transform cancer treatments. 

We now appreciate that at diagnosis, patients with T-cell leukaemia have more than 10 mutations. Some of these mutations will be sufficient to cause leukaemia, but the role of the majority of these mutations remains unknown. 

My research program is focussed on defining the functional role for mutations found in T-cell acute lymphoblastic leukaemia. We utilise a “functional genomics” approach, that is creating in vitro and in vivo mouse models of T-cell leukaemia using clinically relevant mutations, to identify the key proteins and signalling pathways that should be targeted to control the disease. 

This knowledge on which proteins and mutations are essential to drive the growth and survival of leukaemia cells will significantly improve our ability to use targeted agents based on an individual’s mutation signature.