Honorary Professor John Hooper
Honorary Professor

John Hooper

Email: 

Background

1991-94 BSc Honours I (Chemistry) University of Queensland, University Medal

1995-99 PhD (Cancer Pathology) University of Queensland

1999-00 Post-Doctoral Fellow, Queensland University of Technology

2001-03 NHMRC CJ Martin/RG Menzies Fellow, Scripps Research Institute, San Diego, CA, USA

2003-05 NHMRC CJ Martin/RG Menzies Fellow, Queensland University of Technology

2005-09 NHMRC RD Wright Fellow, Queensland University of Technology

2010-15 Associate Professor, Mater Research Institute, The University of Queensland

2012-16 ARC Future Fellow, Mater Research Institute, The University of Queensland

2016- Professor of Cancer Biology, Mater Research Institute, The University of Queensland

Availability

Honorary Professor John Hooper is:
Available for supervision

Fields of research

Biomedical and Clinical Sciences Cancer cell biology Cancer diagnosis Cancer therapy (excl. chemotherapy and radiation therapy) Oncology and carcinogenesis

Research interests

  • Cancers of the urological system, gynaecological system and gastrointestinal tract

    Our focus is on the identification and evaluation of molecular targets and biomarkers of cancer. As much as possible our research employs disease relevant models that incorporate patient tumours. We have developed a successful R&D pipeline to identify cell surface receptors that are enriched in cancer for the purpose of targeting them for delivery of radiation and cytotoxins for cancer detection and treatment. This has culminated in a PET-CT imaging clinical trial evaluating a new radio-imaging agent to guide targeted therapy for ovarian and bladder cancer. My team is expert in generating and employing in vitro, ex vivo and mouse models of cancer, using patient specimens for much of this work. We have extensive experience in cell and molecular biology, protein analysis, including generation, purification and characterisation of recombinant proteins from insect and mammalian cells, enzymology, wide field fluorescent and confocal microscopy of live and fixed specimens, flow cytometry analysis and fluorescent activated cell sorting, bioluminescent and PET/CT imaging of mouse models of cancer, and histological and immunohistochemical analysis of mouse xenografts and patient tumours. We also have expertise in radio- and cytotoxin-labelling of biomolecules using these for detection and treatment of cancer in preclinical models. Our discovery and translational research activities are supported by close collaborations with medical specialists involved in treatment and diagnosis of cancer at Mater, Royal Brisbane and Women’s, Wesley, and Princess Alexandra Hospitals.

Research impacts

My major research contributions are in the identification and evaluation of molecular targets and biomarkers for cancers of the ovary, pancreas, prostate and bowel. At a molecular level my focus is on cell surface receptors, proteolytic enzymes, intracellular signal transducers, mediators of metabolism and protein post-translational modifications. Most recently we have developed a successful R&D pipeline to identify cell surface receptors that are enriched in cancer for the purpose of targeting them for delivery of radiation and cytotoxins for cancer detection and treatment. This has culminated in phase 1 PET-CT imaging clinical trials evaluating the safety and tumour/normal biodistribution of a new radio-imaging agent to guide targeted therapy for ovarian and bladder cancer. My team is expert in generating and employing in vitro, ex vivo and mouse models of cancer, using patient specimens for much of this work. We have extensive experience in cell and molecular biology, protein analysis, including generation, purification and characterisation of recombinant proteins from insect and mammalian cells, enzymology, wide field fluorescent and confocal microscopy of live and fixed specimens, flow cytometry analysis and fluorescent activated cell sorting, bioluminescent and PET/CT imaging of mouse models of cancer, and histological and immunohistochemical analysis of mouse xenografts and patient tumours. We also have expertise in radio- and cytotoxin-labelling of biomolecules using these for detection and treatment of cancer in preclinical models. Our discovery and translational research activities are supported by close collaborations with medical specialists involved in treatment and diagnosis of cancer at Mater, Royal Brisbane and Women’s, Wesley, and Princess Alexandra Hospitals. To date my research has attracted ~$17M in funding, producing 4 patents and 128 papers.

Search Professor John Hooper’s works on UQ eSpace

165 works between 1999 and 2025
All (165) Journal Article (123) Book Chapter (6) Conference Publication (34) Other Outputs (2)

121 - 140 of 165 works

2012

Journal Article

The cell surface glycoprotein CUB domain-containing protein 1 (CDCP1) contributes to epidermal growth factor receptor-mediated cell migration

Dong, Ying, He, Yaowu, de Boer, Leonore, Stack, M. Sharon, Lumley, John W., Clements, Judith A. and Hooper, John D. (2012). The cell surface glycoprotein CUB domain-containing protein 1 (CDCP1) contributes to epidermal growth factor receptor-mediated cell migration. Journal of Biological Chemistry, 287 (13), 9792-9803. doi: 10.1074/jbc.M111.335448

The cell surface glycoprotein CUB domain-containing protein 1 (CDCP1) contributes to epidermal growth factor receptor-mediated cell migration

2012

Book Chapter

Kallikrein-related peptidases (KLKs), Proteinase-mediated signaling and proteinase-activated receptors (PARs)

Hollenberg, Morley D., Hooper, John D., Darmoul, Dalila and Oikonomopoulou, Katerina (2012). Kallikrein-related peptidases (KLKs), Proteinase-mediated signaling and proteinase-activated receptors (PARs). Characterization, regulation, and interactions within the protease web. (pp. 373-398) Berlin, Germany: De Gruyter Mouton.

Kallikrein-related peptidases (KLKs), Proteinase-mediated signaling and proteinase-activated receptors (PARs)

2012

Book Chapter

Kallikrein-related peptidases (KLKs), Proteinase-mediated Signalling and Proteinase-activated receptors (PARs)

Hollenberg, M.D. and Hooper, John David (2012). Kallikrein-related peptidases (KLKs), Proteinase-mediated Signalling and Proteinase-activated receptors (PARs). Kallikrein-related peptidases Volume 1, Characterization, regulation, and interactions within the protease web. (pp. 373-398) edited by Viktor Magdolen, Christian Sommerhoff, Hans Fritz and Manfred Schmitt. Berlin Germany: DeGruyter.

Kallikrein-related peptidases (KLKs), Proteinase-mediated Signalling and Proteinase-activated receptors (PARs)

2012

Book Chapter

Endogenous strategies for steroidogenesis and androgen signalling in prostate cancer cells

Bennett, Nigel C., Hooper, John and Gobe, Glenda C. (2012). Endogenous strategies for steroidogenesis and androgen signalling in prostate cancer cells. Androgens: production, functions and disorders. (pp. 99-114) edited by Berkley F. Thompson and Devon J. Robinson. New York, NY, United States: Nova Science Publishers.

Endogenous strategies for steroidogenesis and androgen signalling in prostate cancer cells

2012

Journal Article

Evaluation of antibodies directed against human protease-activated receptor-2

Adams, Mark N., Pagel, Charles N., Mackie, Eleanor J. and Hooper, John D. (2012). Evaluation of antibodies directed against human protease-activated receptor-2. Naunyn-Schmiedeberg's Archives of Pharmacology, 385 (9), 861-873. doi: 10.1007/s00210-012-0783-6

Evaluation of antibodies directed against human protease-activated receptor-2

2011

Journal Article

Cellular settings mediating Src substrate switching between focal adhesion kinase tyrosine 861 and CUB-domain-containing protein 1 (CDCP1) tyrosine 734

Wortmann, Andreas, He, Yaowu, Christensen, Melinda E., Linn, Mayla, Lumley, John W., Pollock, Pamela M., Waterhouse, Nigel J. and Hooper, John D. (2011). Cellular settings mediating Src substrate switching between focal adhesion kinase tyrosine 861 and CUB-domain-containing protein 1 (CDCP1) tyrosine 734. Journal of Biological Chemistry, 206 (49), 42303-42315. doi: 10.1074/jbc.M111.227462

Cellular settings mediating Src substrate switching between focal adhesion kinase tyrosine 861 and CUB-domain-containing protein 1 (CDCP1) tyrosine 734

2011

Journal Article

The role of palmitoylation in signalling, cellular trafficking and plasma membrane localization of protease-activated receptor-2

Adams, Mark N., Christensen, Melinda E., He, Yaowu, Waterhouse, Nigel J. and Hooper, John D. (2011). The role of palmitoylation in signalling, cellular trafficking and plasma membrane localization of protease-activated receptor-2. PLoS One, 6 (11) e28018, 1-14. doi: 10.1371/journal.pone.0028018

The role of palmitoylation in signalling, cellular trafficking and plasma membrane localization of protease-activated receptor-2

2011

Journal Article

Structure, function and pathophysiology of protease activated receptors

Adams, Mark N., Ramachandran, Rithwik, Yau, Mei-Kwan, Suen, Jacky Y., Fairlie, David P., Hollenberg, Morley D. and Hooper, John D. (2011). Structure, function and pathophysiology of protease activated receptors. Pharmacology and Therapeutics, 120 (3), 248-282. doi: 10.1016/j.pharmthera.2011.01.003

Structure, function and pathophysiology of protease activated receptors

2010

Journal Article

Proteolysis-induced N-terminal ectodomain shedding of the integral membrane glycoprotein CUB domain-containing protein 1 (CDCP1) is accompanied by tyrosine phosphorylation of its C-terminal domain and recruitment of Src and PKC delta

He, Yaowu, Wortmann, Andreas, Burke, Les J., Reid, Janet C., Adams, Mark N., Abdul-Jabbar, Ibtissam, Quigley, James P., Leduc, Richard, Kirchhofer, Daniel and Hooper, John D. (2010). Proteolysis-induced N-terminal ectodomain shedding of the integral membrane glycoprotein CUB domain-containing protein 1 (CDCP1) is accompanied by tyrosine phosphorylation of its C-terminal domain and recruitment of Src and PKC delta. Journal of Biological Chemistry, 285 (34), 26162-26173. doi: 10.1074/jbc.M109.096453

Proteolysis-induced N-terminal ectodomain shedding of the integral membrane glycoprotein CUB domain-containing protein 1 (CDCP1) is accompanied by tyrosine phosphorylation of its C-terminal domain and recruitment of Src and PKC delta

2010

Journal Article

The cutting edge: Membrane-anchored serine protease activities in the pericellular microenvironment

Antalis, Toni M., Buzza, Marguerite S., Hodge, Kathryn M., Hooper, John D. and Netzel-Arnett, Sarah (2010). The cutting edge: Membrane-anchored serine protease activities in the pericellular microenvironment. Biochemical Journal, 428 (3), 325-346. doi: 10.1042/BJ20100046

The cutting edge: Membrane-anchored serine protease activities in the pericellular microenvironment

2010

Journal Article

Molecular cell biology of androgen receptor signalling

Bennett, Nigel C., Gardiner, Robert A., Hooper, John D., Johnson, David W. and Gobe, Glenda C. (2010). Molecular cell biology of androgen receptor signalling. International Journal of Biochemistry and Cell Biology, 42 (6), 813-827. doi: 10.1016/j.biocel.2009.11.013

Molecular cell biology of androgen receptor signalling

2009

Journal Article

Androgen Receptor and Caveolin-1 in Prostate Cancer

Bennett, Nigel, Hooper, John D., Lee, C. Soon and Gobe, Glenda C. (2009). Androgen Receptor and Caveolin-1 in Prostate Cancer. IUBMB Life, 61 (10), 961-970. doi: 10.1002/IUB.244

Androgen Receptor and Caveolin-1 in Prostate Cancer

2009

Journal Article

The Glycosylphosphatidylinositol-Anchored Serine Protease PRSS21 (Testisin) Imparts Murine Epididymal Sperm Cell Maturation and Fertilizing Ability

Sarah Netzel-Arnett, Thomas H. Bugge, Rex A. Hess, Kay Carnes, Brett W. Stringer, Anthony L. Scarman, John D. Hooper, Ian D. Tonks, Graham F. Kay and Toni M. Antalis (2009). The Glycosylphosphatidylinositol-Anchored Serine Protease PRSS21 (Testisin) Imparts Murine Epididymal Sperm Cell Maturation and Fertilizing Ability. Biology of Reproduction, 81 (5), 921-932. doi: 10.1095/biolreprod.109.076273

The Glycosylphosphatidylinositol-Anchored Serine Protease PRSS21 (Testisin) Imparts Murine Epididymal Sperm Cell Maturation and Fertilizing Ability

2009

Journal Article

Substrate-guided design of a potent and selective kallikrein-related peptidase inhibitor for kallikrein 4

Swedberg, Joakim E., Nigon, Laura V., Reid, Janet C., de Veer, Simon J., Walpole, Carina M., Stephens, Carson R., Walsh, Terry P., Takayama, Thomas K., Hooper, John D., Clements, Judith A., Buckle, Ashley M. and Harris, Jonathan M. (2009). Substrate-guided design of a potent and selective kallikrein-related peptidase inhibitor for kallikrein 4. Chemistry and Biology, 16 (6), 633-643. doi: 10.1016/j.chembiol.2009.05.008

Substrate-guided design of a potent and selective kallikrein-related peptidase inhibitor for kallikrein 4

2009

Journal Article

The cell surface glycoprotein CDCP1 in cancer - Insights, opportunities, and challenges

Wortmann, Andreas, He, Yaowu, Deryugina, Elena I., Quigley, James P. and Hooper, John D. (2009). The cell surface glycoprotein CDCP1 in cancer - Insights, opportunities, and challenges. IUBMB Life, 61 (7), 723-730. doi: 10.1002/iub.198

The cell surface glycoprotein CDCP1 in cancer - Insights, opportunities, and challenges

2009

Conference Publication

Kallikrein-related proteases as novel therapeutic targets in prostate and ovarian cancer

Clements, J. A., Dong, Y., Loessner, D., Tan, O., Sieh, S., Reichert, J., Burke, L., Stephens, C., Lawrence, M., Stansfield, S., Swedberg, J., Ramsay, A., Hooper, J., Harris, J. and Hutmacher, D. (2009). Kallikrein-related proteases as novel therapeutic targets in prostate and ovarian cancer. 40th Annual Conference of the Society for Reproductive Biology, Clayton, VIC, Australia: CSIRO Publishing. doi: 10.1071/srb09abs009

Kallikrein-related proteases as novel therapeutic targets in prostate and ovarian cancer

2009

Journal Article

Functional role of cell surface CUB domain-containing protein 1 in tumor cell dissemination

Deryugina, Elena I., Conn, Erin M., Wortmann, Andreas, Partridge, Juneth J., Kupriyanova, Tatyana A., Ardi, Veronica C., Hooper, John D. and Quigley, James P. (2009). Functional role of cell surface CUB domain-containing protein 1 in tumor cell dissemination. Molecular Cancer Research, 7 (8), 1197-1211. doi: 10.1158/1541-7786.MCR-09-0100

Functional role of cell surface CUB domain-containing protein 1 in tumor cell dissemination

2009

Journal Article

Matriptase-2 (TMPRSS6): A proteolytic regulator of iron homeostasis

Ramsay, Andrew J., Hooper, John D., Folgueras, Alicia R., Velasco, Gloria and Lopez-Otin, Carlos (2009). Matriptase-2 (TMPRSS6): A proteolytic regulator of iron homeostasis. Haematologica, 94 (6), 840-849. doi: 10.3324/haematol.2008.001867

Matriptase-2 (TMPRSS6): A proteolytic regulator of iron homeostasis

2008

Journal Article

The ubiquitin-protein ligase Nedd4-2 differentially interacts with and regulates members of the Tweety family of chloride ion channels

He, Yaowu, Hryciw, Deanne H., Carroll, Melanie L., Myers, Stephen A., Whitbread, Astrid K., Kumar, Sharad, Poronnik, Philip and Hooper, John D. (2008). The ubiquitin-protein ligase Nedd4-2 differentially interacts with and regulates members of the Tweety family of chloride ion channels. Journal of Biological Chemistry, 283 (35), 24000-24010. doi: 10.1074/jbc.M803361200

The ubiquitin-protein ligase Nedd4-2 differentially interacts with and regulates members of the Tweety family of chloride ion channels

2008

Journal Article

N-glycosylation analysis of the human Tweety family of putative chloride ion channels supports a penta-spanning membrane arrangement: impact of N-glycosylation on cellular processing of Tweety homologue 2 (TTYH2)

He, Yaowu, Ramsay, Andrew, Hunt, Melanie, Whitbread, Astrid, Myers, Stephen and Hooper, John (2008). N-glycosylation analysis of the human Tweety family of putative chloride ion channels supports a penta-spanning membrane arrangement: impact of N-glycosylation on cellular processing of Tweety homologue 2 (TTYH2). Biochemical Journal, 412 (1), 45-55. doi: 10.1042/BJ20071722

N-glycosylation analysis of the human Tweety family of putative chloride ion channels supports a penta-spanning membrane arrangement: impact of N-glycosylation on cellular processing of Tweety homologue 2 (TTYH2)

Availability

Honorary Professor John Hooper is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • Cellular targets for cancer detection and treatment

    The project involves the use of state-of-the-art in silico and omics approaches to identify antigens that are suitable targets for delivery of radioactive and cytotoxic payloads to cancers. Candidates will be validated by analysis of patient tumours and normal organs.

  • Agents for targeted delivery of cytotoxins to cancer

    A range of screening approaches will be employed to identify organic compounds, peptides and antibodies that bind with high affinity and specificity to antigens enriched on the surface of cancer cells. The efficacy of these agents for delivery of payloads to cancer will be evaluated using cellular and mouse models of cancer.

  • Disrupting metabolsim to improve cancer treatment efficacy

    The project will employ disease-relevant in vitro mouse models to test metabolism modulating approaches to improve the efficacy of current anti-cancer treatments.

  • Targeting cell division to significatly improve the effectiveness of ovarian cancer treatments

    The project will employ nanoparticle formulations of cell division disrupting drugs against patient-derived in vitro, ex vivo and in vivo models of high-grade serous ovarian cancer.

Supervision history

Current supervision

  • Doctor Philosophy

    Cancer-associated post-translational modifications of the receptor CDCP1 Background:

    Principal Advisor

  • Doctor Philosophy

    Understanding the function of CDCP1 and its potential as a theranostic target for cholangiocarcinoma

    Principal Advisor

    Other advisors: Professor Kristofer Thurecht

  • Doctor Philosophy

    Novel Theranostic Targets for Colorectal Cancer

    Principal Advisor

    Other advisors: Professor David Clark

  • Doctor Philosophy

    Factors impacting receptor processing in response to peptide and antibody ligands

    Principal Advisor

    Other advisors: Dr Jodi Saunus

  • Doctor Philosophy

    Molecular and cellular determinants of CDCP1 targeted, payload-delivery antibodies.

    Principal Advisor

    Other advisors: Associate Professor Michael Landsberg

  • Doctor Philosophy

    Development of antibody-drug conjugates against hard-to-cure solid cancers

    Associate Advisor

    Other advisors: Dr Brett Paterson, Associate Professor Fernando Guimaraes

  • Doctor Philosophy

    Developing new strategies to overcome immune suppression in cancer

    Associate Advisor

    Other advisors: Dr Sherry Wu

  • Doctor Philosophy

    Developing novel strategies to overcome immune suppression in cancer

    Associate Advisor

    Other advisors: Dr Sherry Wu

  • Doctor Philosophy

    Enhancing immune responses to cancer

    Associate Advisor

    Other advisors: Dr Jazmina Gonzalez Cruz, Professor Brian Gabrielli

  • Doctor Philosophy

    Genomic and epigenomic correlates of prostate cancer therapy

    Associate Advisor

    Other advisors: Associate Professor Adam Ewing

  • Doctor Philosophy

    Characterisation of EV-associated lipids in the progression of ovarian cancer

    Associate Advisor

    Other advisors: Dr Dominic Guanzon, Professor Carlos Salomon Gallo, Dr Andrew Lai

Completed supervision

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