Projects per year
Personal profile
Administrative Posts
- Course Director C100 Biological Sciences
- Member of Exam Board
- Chairman of BIO Library Committee
- Member of GMO Committee
- BIO Coursework Co-ordinator
Biography
BSc from Birmingham University in 1985, and a PhD from the University of London in 1989. He was a postdoctoral fellow at Oxford University (1989-1991), and then an Alexander vonHumboldt Fellow at the Max-Planck Institute in Martinsried (1991-1993), working in Prof. Axel Ullrich’s laboratory. His first independent research group set up in 1993 at Imperial College made significant contributions to defining novel cellular pathways that regulate cell surface receptor activation and dimerisation. This led to the first evidence that transmembrane receptor kinases have specific intracellular dimerisation domains that are essential for receptor activation. Other studies have led to the identification of important cross-talk regulatory mechanisms between receptor tyrosine kinases and calcium signalling pathways. Following his move to UEA in 2000, he began to define novel links between receptor tyrosine kinases and transforming growth factor-b (TGFb), and was the first to demonstrate pathway integration between cytosolic calcium and signalling molecules known as Smad transcription factors. Recently, he established for the first time novel mechanisms for controlling Smad signalling by reversible ubiquitination, linking HECT E3 ubiquitin ligases and deubiquitinating enzymes to TGFb-dependent tumour outgrowth/metastasis.
Career
- Senior Lecturer in Cell Biology, University of East Anglia (2000-present)
- Lecturer, Department of Cancer Medicine, Imperial College (1993-2000)
- Alexander von Humboldt Fellow, Max-Planck-Institute, Munich (1991-1993)
- Postdoctoral Fellow, University of Oxford (1989-1991)
- Ph.D. University of London (1989)
- B.Sc. Medical Biochemistry, University of Birmingham (1985)
Key Research Interests
At present, his laboratory has a translational and drug discovery focus, and has projects aimed at developing novel therapeutic strategies targeting abnormal TGFb activity in cancer metastasis, leukaemia, osteoarthritis, and fibrotic disease.
Current research projects;
- Novel therapeutics targeting the WWP2 Ubiquitin Ligase oncogene in malignant melanoma Novel Regulation of TGFb signalling by a protein kinase over-expressed in Breast Cancer
- A new dual therapy approach for the treatment of chronic myeloid leukaemia
- A new approach to target abnormal chondrocyte growth in osteoarthritis and the aging joint’
PhD Positions
Click here for current PhD opportunities in Biological Sciences. But feel free to email me to discuss projects outside these areas and alternative sources of funding.
Teaching Interests
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Collaborations and top research areas from the last five years
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Synthesis and evaluation of X-ray structure inspired ubiquitin ligase inhibitors as anticancer lead compounds
Hemmings, A., Angulo, J., Chantry, A., Hemmings, A., Stephenson, G. R. & Storr, T.
1/10/20 → 31/03/25
Project: Research
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Developing novel protein degradation tools and technologies as cancer therapeutics
Chantry, A. & Hughes, G.
1/09/19 → 31/03/21
Project: Research
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Structural studies of novel ubiquitin ligase inhibitors to develop their therapeutic potential
1/08/19 → 25/09/19
Project: Research
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Astra Zeneca Collaboration
Chantry, A., Bulman Page, P., Hemmings, A. & Stephenson, G. R.
1/08/17 → 31/10/18
Project: Research
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3,3′-Diindolylmethane (DIM): A molecular scaffold for inhibition of WWP1 and WWP2, members of the NEDD4 family HECT E3 ligases
Dudey, A. P., Hughes, G. R., Rigby, J. M., Monaco, S., Stephenson, G. R., Storr, T. E., Angulo, J., Chantry, A. & Hemmings, A. M., 18 Feb 2025, In: ACS Omega. 10, 6, p. 5963–5972 10 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
An improved synthesis of 2,3-diamino-5,6-dichloropyrazine: A useful heterocyclic scaffold
Rigby, J. M., Chantry, A., Hemmings, A. M., Richards, C. J., Stephenson, G. R. & Storr, T. E., Dec 2024, In: Synthesis. 56, 23, p. 3587-3592 6 p.Research output: Contribution to journal › Article › peer-review
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Expanding the inhibitor space of the WWP1 and WWP2 HECT E3 ligases
Dudey, A. P., Rigby, J. M., Hughes, G. R., Stephenson, G. R., Storr, T. E., Chantry, A. & Hemmings, A. M., 3 Sept 2024, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 39, 1, 2394895.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Frontiers in PROTACs
Hughes, G. R., Dudey, A. P., Hemmings, A. M. & Chantry, A., Oct 2021, In: Drug Discovery Today. 26, 10, p. 2377-2383 7 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
WW domains from WWP2 E3 ubiquitin ligase recognise Oct4 and Smad7 peptides
Wahl, L. C., Watt, J. E., De Bourcier, D., Chantry, A. & Blumenschein, T. M. A., 7 Feb 2020, In: Biophysical Journal. 118, 3, p. 182a 1 p.Research output: Contribution to journal › Abstract › peer-review
Open Access
Activities
- 2 Publication editorial role
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Frontiers in Molecular and Structural Endocrinology (Journal)
Andrew Chantry (Editorial board member)
2010 → 2015Activity: Editorial work › Publication editorial role
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Molecular & Cellular Proteomics (Journal)
Andrew Chantry (Editorial board member)
2006 → 2016Activity: Editorial work › Publication editorial role