Adelaide Medical School
Faculty of Health and Medical Sciences
Eligible to supervise Masters and PhD - email supervisor to discuss availability.
Professor Betty Sallustio
Position: Principal Medical Scientist
Group: Basil Hetzel Institute for Translational Health Research
Department: Clinical Pharmacology
Professor Sallustio is Principal Medical Scientist in the Department of Clinical Pharmacology at the Queen Elizabeth Hospital, where she manages the Therapeutic Drug Monitoring service. She is also Affiliate Professor in the Discipline of Pharmacology at Adelaide University, and has research interests in pharmacogenomics of renal transplantation, the clinical pharmacology of myocardial metabolic agents, and the role of UGTs in bioactivation of drugs.
Professor Sallustio is a long-standing member of the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists, and currently serves as co-chair of its Therapeutic Drug Monitoring working group. She is a Fellow of the Faculty of Science of the Royal College of Pathologists of Australia and is also the secretary of the Special Drugs Working Party of the Australasian Association of Clinical Biochemists.
- My Research
- Grants and Funding
- Professional Activities
Our Research Group
Professor Sallustio leads the Clinical Pharmacology Unit based at the Basil Hetzel Institute for Translational Health Research. The Basil Hetzel Institute for Translational Health Research is part of The Queen Elizabeth Hospital, and researchers work closely with the hospital’s clinical divisions, and have a focus on translational health research, an innovative ‘bench to bedside’ approach in which scientific discoveries can be quickly translated into improved patient care and treatment. The institute offers a range of postgraduate and honours training opportunities each year for PhD, Masters and Honours students.
The Clinical Pharmacology Unit is affiliated with the Discipline of Pharmacology of the University of Adelaide. It provides a clinical therapeutic drug monitoring service coupled with an active research program in the areas of heart disease, kidney transplantation and cancer.
Professor Sallustio’s research interests include drug biotransformation and transport, particularly understanding how inter-individual differences in these processes, either genetic or environmental, impact on drug toxicity and clinical efficacy. She has pursued three main arms of research: i) the role of biotransformation in enhancing drug toxicity, particularly intracellular protein and genetic damage; ii) applying an understanding of variability in the biotransformation and cellular transport of immunosuppressants to improving clinical outcomes in renal transplant recipients; and iii) understanding the role of energetics in heart disease and cancer. This work has been supported by major competitive funding from the National Heart Foundation, the Anti Cancer Foundation, the National Health and Medical Research Council, Cancer Council SA, and the Juvenile Diabetes Research Foundation.
Metabolic Treatments for Heart Disease and Cancer
Altered cellular energy metabolism is an underlying feature of both heart disease and cancer. In heart disease, maladaptive changes in energy utilisation and storage contribute to a decline in myocardial function and structural remodelling. In cancer cells, changes in energy utilisation allow increased cell survival, replication and metastasis. In addition, a number of cancer chemotherapy agents cause myocardial damage. Therefore, it is possible that myocardial metabolic agents designed for treatment of heart disease, may also be useful adjunct therapy in cancer. PhD and Honours projects are available in two broad research areas:
1. Investigating the efficacy of new myocardial metabolic agents in the treatment of heart failure and ischaemic heart disease.
2. Developing new therapies for chemotherapy-induced myocardial toxicity in cancer patients
Individualising Transplantation Therapy
The success of kidney transplantation depends largely on preventing rejection of the new organ, using a combination of immunosuppressant drugs. These drugs have narrow therapeutic indices and can cause renal, gastrointestinal or haematological toxicity. Due to significant variability in their elimination from the body, doses are currently individualised by targeting therapeutic concentrations in blood. Despite this, rejection and toxicity still occur. Our research focuses on understanding immunosuppressant distribution into lymphocytes (the mediators of rejection) and renal tissue (a major site of toxicity), as a means of better predicting individual risk of rejection and damage to the transplanted organ. PhD and Honours projects are available in two broad areas of research:
1. To investigate genetic variability in the pathways of immunosuppressant elimination in both kidney donors and recipients, to determine its impact on intra-renal and intra-lymphocyte exposure to immunosuppressants, and its association with rejection and long-term function of the transplanted kidney.
2. To investigate how pregnancy alters the pharmacokinetics of immunosuppressants in renal transplant recipients, and to develop biomarkers that may be used in conjunction with standard monitoring to minimise the risk of nephrotoxicity and graft loss during pregnancy.
Date Position Institution name 2010 Affiliate Associate Professor University of Adelaide 1998 Principal Medical Scientist Queen Elizabeth Hospital, Adelaide
Date Institution name Country Title 1990 Flinders University Australia Ph. D. 1982 University of Adelaide Australia B. Sc.
Date Title Institution name Country 2012 Fellow, Faculty of Science Royal College of Pathologists of Australia —
Year Citation 2017 Chong, C. -R., Imam, H., Sallustio, B., Chirkov, Y., & Horowitz, J. (2017). Perhexiline enhances cGMP- and cAMP-signaling in diabetics independent of insulin sensitization and ACE inhibition. In EUROPEAN HEART JOURNAL Vol. 38 (pp. 1143). OXFORD UNIV PRESS. 2016 Hu, R. (2016). CYP3A5*3 and ABCB1 haplotype 61A-1199G-1236T-2677T/A-3435T are associated with dose-adjusted trough blood tacrolimus concentration in kidney transplant recipients. In ASCEPT-MPGPCR 2016. Melbourne, Australia. 2011 Sallustio, B. C., Noll, B., Coller, J., Somogyi, A., van Gelder, T., Hesselink, D., & Morris, R. G. (2011). LC-MS/MS quantification of tacrolimus concentrations in small samples of kidney and liver tissue. In THERAPEUTIC DRUG MONITORING Vol. 33 (pp. 540). Stuttgart, GERMANY: LIPPINCOTT WILLIAMS & WILKINS. 2009 Licari, J., Somogyi, A., Pierides, J., & Sallustio, B. C. (2009). Comparison of sprague dawley and dark agouti rats as animal models of perhexiline-induced hepatotoxicity. In DRUG METABOLISM REVIEWS Vol. 41 (pp. 128). Baltimore, MD: TAYLOR & FRANCIS INC. 2009 Sallustio, B., Westley, I., Coller, J., Ward, M., Russ, G., & Morris, R. (2009). Frequency of Genetic Polymorphisms in the Promoter (C-24T), Exon 10 (G1249A) and Exon 28 (C3972T) Regions of ABCC2 in Australian Renal Transplant Recipients and Donors. In THERAPEUTIC DRUG MONITORING Vol. 31 (pp. 656-657). Montreal, CANADA: LIPPINCOTT WILLIAMS & WILKINS. 2009 Sallustio, B. C., & Morris, R. (2009). Total bilirubin concentrations in plasma of renal transplant patients may reflect differences in MRP2 inhibition by cyclosporine and tacrolimus. In DRUG METABOLISM REVIEWS Vol. 41 (pp. 77-78). Baltimore, MD: TAYLOR & FRANCIS INC. 2007 Sallustio, B. C., Southwood, H. T., DeGraaf, Y. C., Mackenzie, P. I., Miners, J. O., & Burcham, P. C. (2007). GLUCURONIDATION-DEPENDENT DNA NICKING BY CARBOXYLIC ACID DRUGS IN HEK293 CELLS EXPRESSING HUMAN UDP-GLUCURONOSYLTRANSFERASES. In DRUG METABOLISM REVIEWS Vol. 39 (pp. 144-145). Sendai, JAPAN: TAYLOR & FRANCIS INC. 2007 Westley, I., Morris, R., Evans, A., & Sallustio, B. (2007). Glucuronidation of mycophenolic acid by Wistar and mrp2 deficient TR- rat liver microsomes: Effect of mycophenolate acyl glucuronide, cyclosporin and metabolites AM1, AM1c and AM9. In THERAPEUTIC DRUG MONITORING Vol. 29 (pp. 473-474). Nice, FRANCE: LIPPINCOTT WILLIAMS & WILKINS. 2007 Sallustio, B. C., Davies, B. J., Herbert, M. K., Coller, J. K., Somogyi, A. A., & Milne, R. W. (2007). Steady-state pharmacokinetics of the enantiomers of perhexiline in CYP2D6 extensive and poor metabolisers. In THERAPEUTIC DRUG MONITORING Vol. 29 (pp. 478). Nice, FRANCE: LIPPINCOTT WILLIAMS & WILKINS. 2006 Westley, I., Morris, R., Evans, A., & Sallustio, B. (2006). Mycophenolic acid metabolism in Wistar and Mrp2 transporter deficient TR-rat microsomes.. In ACTA PHARMACOLOGICA SINICA Vol. 27 (pp. 221). BLACKWELL PUBLISHING. 2005 Sallustio, B., Westley, I., Brogen, L., Morris, R., & Evans, A. (2005). Effect of cyclosporin on the hepatic disposition of mycophenolic acid. In THERAPEUTIC DRUG MONITORING Vol. 27 (pp. 251). Louisville, KY: LIPPINCOTT WILLIAMS & WILKINS.
2004 Westley, I., Sallustio, B., Morris, R., Evans, A., & Brogan, L. (2004). Cyclosporin-mycophenolate drug interaction: Role of Mrp2. In DRUG METABOLISM REVIEWS Vol. 36 (pp. 61). Vancouver, CANADA: TAYLOR & FRANCIS INC. 2004 Sallustio, B., DeGraaf, Y., & Burcham, P. (2004). Detection of UGT-dependent DNA damage in mammalian cells. In DRUG METABOLISM REVIEWS Vol. 36 (pp. 236). Vancouver, CANADA: TAYLOR & FRANCIS INC. 2001 Sallustio, B., Weekley, J., & Burcham, P. (2001). Clofibric acid glucuronide-induced DNA strand nicking: role of hydroxyl radical formation. In TOXICOLOGY Vol. 164 (pp. 103). ELSEVIER SCI IRELAND LTD. 1983 SALLUSTIO, B., MEFFIN, P., BROOKS, P., & WING, L. (1983). PREDNISOLONE DISPOSITION AS A FUNCTION OF DOSE AND ORAL-CONTRACEPTIVE USE. In CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY Vol. 10 (pp. 667). BLACKWELL SCIENCE.
Year Citation 2015 Dom, Z., Westley, I., Coller, J., Somogyi, A., & Sallustio, B. (2015). Multidrug Resistance-Associated Protein 2 (MRP2/ABCC2) haplotypes significantly affect the pharmacokinetics of mycophenolic acid in renal transplant recipients. Poster session presented at the meeting of Abstracts of the 2015 Golden Helix Symposium - Next Generation Pharmacogenomics, as published in Public Health Genomics. Karger.
2015 Dom, Z. M., Coller, J., Carroll, R., Somogyi, A., & Sallustio, B. (2015). Intra-Lymphocyte Concentrations of Mycophenolic Acid Correlate With the Incidence of Early Graft Rejection in Renal Transplant Recipients. Poster session presented at the meeting of AMERICAN JOURNAL OF TRANSPLANTATION. Philadelphia, PA: WILEY-BLACKWELL. 2014 Westley, I. S., Licari, G., Watts, R. W., & Sallustio, B. C. (2014). IDENTIFICATION OF ALTERED PROTEIN BINDING OF DEXAMETHASONE IN THE PRESENCE OF SUGAMMADEX. Poster session presented at the meeting of DRUG METABOLISM REVIEWS. Toronto, CANADA: INFORMA HEALTHCARE. 2013 Sallustio, B., Noll, B., Coller, J., & Somogyi, A. (2013). Association Between Intra-Renal P-gp Expression and Cyclosporine Concentrations in Renal Transplantation. Poster session presented at the meeting of THERAPEUTIC DRUG MONITORING. Salt Lake City, UT: LIPPINCOTT WILLIAMS & WILKINS. 2013 Dom, M. Z., Coller, J., Somogyi, A., & Sallustio, B. (2013). Impact of Recipient and Donor Multidrug Resistance Protein 2 Genetic Variability on Mycophenolic Acid Pharmacokinetics Following Kidney Transplantation. Poster session presented at the meeting of THERAPEUTIC DRUG MONITORING. Salt Lake City, UT: LIPPINCOTT WILLIAMS & WILKINS. 2012 Westley, I., Bezak, E., Sjostedt, S., Sallustio, B., & Licari, G. (2012). Investigation of the Role of Acid Sphingomyelinase in the Bystander Effects of Breast Cancer Cell Irradiation. Poster session presented at the meeting of EUROPEAN JOURNAL OF CANCER. Barcelona, SPAIN: ELSEVIER SCI LTD.
Research Funding (last 5 years)
|Year||Amount||Funding Body, Chief Investigators, Project Title|
2012 - 2013
|$130,000||National Heart Foundation - Grant-in-aid: BC Sallustio, JD Horowitz, JA Kennedy, MP Frenneaux, “Utility of (+)- and (-)-perhexiline as model compounds for the development of new myocardial metabolic agents”.|
|2014 - 2015||$150,000||Adelaide Research and Innovation, Commercial funding from Heat Metabolics Ltd. BC Sallustio.|
|2016||$75,000||Cancer SA – Beat Cancer Project: BC Sallustio, A Evdokiou, JD Horowitz, “Prevention of heart damage during anthracycline cancer chemotherapy”.|
|2017||$302,000||University of Adelaide Equipment Round 2016. AA Somogyi, BC Sallustio, JK Coller, M Hutchinson, D Barratt.|
|2018-2020||$327,214||NHMRC – Project Grant (APP1145776), BC Sallustio, A Evdokiou, JD Horowitz, “Prevention of heart damage during anthracycline cancer chemotherapy”.|
As an affiliate of the Discipline of Pharmacology Professor Sallustio contributes to both undergraduate and postgraduate teaching. She teaches aspects of drug metabolism and personalised medicine in PHARM 3011 - Drug Development and Therapeutics, and supervises both Honours and PhD students enrolled in the discipline.
Current Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 2019 Principal Supervisor Using Pharmacokinetic Principles to Improve the Safety of Tacrolimus in Kidney Transplant Recipients Doctor of Philosophy Doctorate Full Time Miss Mirabel Alonge
Past Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 2015 - 2019 Co-Supervisor Genetics of Tacrolimus Pharmacokinetics and Kidney Transplant Outcomes Doctor of Philosophy Doctorate Full Time Ms Rong Hu 2012 - 2017 Principal Supervisor A Pharmacological Approach Towards Myocardial Protection: New Perspectives in Acute and Chronic Cardiac Disease Doctor of Philosophy Doctorate Full Time Miss Cher-Rin Chong 2011 - 2017 Principal Supervisor Mycophenolic Acid Pharmacokinetics and Clinical Outcomes in Renal Transplantation: Effect of ABCC2 Haplotype Analysis and Distribution into Lymphocytes and Kidney Doctor of Philosophy Doctorate Full Time Mr Zaipul Izwan Md Dom 2007 - 2013 Principal Supervisor The Stereoselective Pharmacodynamics of the Enantiomers of Perherhexiline Doctor of Philosophy Doctorate Part Time Dr Johnny Licari 2003 - 2008 Principal Supervisor The Stereoselective Pharmacokinetics of the Enantiomers of Perhexiline in Poor and Extensive Metabolisers of the Cytochrome P450 2D6 Doctor of Philosophy Doctorate Full Time Mr Benjamin Davies
Date Role Committee Institution Country 2015 - ongoing Member Organising Committee, ANZ Therapeutic Drug Monitoring — Australia 2012 - ongoing Co-Chair ASCEPT-APSA TDM Satellite Meeting, Therapeutic Drug Monitoring Fundamentals and Emerging Trends – Focus on Antimicrobials, School of Pharmacy University of Sydney Australia 2011 - ongoing Secretary Australasian Association of Clinical Biochemists - Special Drugs Working Party — Australia 2011 - ongoing Co-Chair Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists - Therapeutic Drug Monitoring Group — Australia 2009 - 2013 Council International Association of Therapeutic Drug Monitoring and Clinical Toxicology — Australia 2009 - ongoing Chair Adelaide Pharmacology Group — Australia 2005 - ongoing Member Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists - Pharmacogenetics Special Interest Group — Australia 2002 - ongoing Board Member Adelaide Pharmacology Group — Australia 1994 - ongoing Member Ethics of Human Research Committee – Scientific Review The Queen Elizabeth Hospital Australia
Date Role Membership Country 1992 - ongoing Member International Association for Therapeutic Drug Monitoring and Clinical Toxicology (IATDMCT). Australia 1990 - 2011 Member International Society for the Study of Xenobiotics (ISSX) Australia 1989 - ongoing Member South Australian Medical Scientists Association Australia 1982 - ongoing Member Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists (ASCEPT). Australia
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