Developing novel chemical tools for the treatment of castration resistant prostate cancer
Start date1 October 2019
Competition funded project that covers the tuition fee for EU/UK students, offering a tax-free yearly stipend of £15,000.
Funding sourceUniversity of Surrey Doctoral College
Prostate cancer (PrCa) is a leading cause of cancer related male mortality in the United Kingdom with over 10,000 deaths each year. The growth and progression of PrCa is regulated by androgens, which manifest their action by activating the androgen receptor (AR), a ligand activated transcription factor that in turn regulates the growth of PrCa. Since AR signaling is upregulated in PrCa, it is an attractive drug target in the treatment of the advanced PrCa.
Hence, widely used androgen deprivation therapy (ADT) is the mainstay treatment for PrCa, which is achieved by the use of anti-androgenic drugs such as Bicalutamide and Enzalutamide. ADT is initially effective but relapse is common leading to castration resistant prostate cancer (CRPC) for which there are no curative treatments.
The key question is why does ADT fail and how can we develop more effective anti-androgens to target the AR? In collaboration with the Department of Chemistry University of Cambridge and Nuffield Department of Surgical Sciences, University of Oxford, this project will discover novel anti-androgens to develop curative treatment for CRPC. The findings of this study will pave the way to effectively treat CRPC in order to alleviate the disease burden.
The research will be done in collaboration with the University of Cambridge and Oxford, where Dr Asim holds honorary scientist posts. The chemical tools will be tested on human cancer tissue specimen available through a collaboration with Professor Hardev Pandha (Royal Surrey County Hospital).
Related linksNuffield Department of Surgical Sciences, University of Oxford
- Anne Y. Warren, Charlie E. Massie, David E. Neal and Mohammad Asim (2018) A reciprocal feedback between the PDZ binding kinase and androgen receptor in prostate cancer. Oncogene 2018 Sep 20. doi: 10.1038/s41388-018-0501-z
- Asim M, Tarish F, Neal DE and Helleday T (2017) Synthetic Lethality between androgen signaling and PARP pathway in Prostate Cancer. Nat Commun. Aug 29;8(1):374
- Asim M, Massie CE & Neal DE (2016) Kinase Joins the Chaperone Club: Androgen-Regulated Kinome Reveals Choline Kinase Alpha as Potential Drug Target in Prostate Cancer. Molecular & Cellular Oncology Feb 24;3(3):e1140262.
- Asim M, Massie CE, Tilley WD, & Neal DE. (2015) Choline kinase alpha is an Androgen Receptor Chaperone and Prostate Cancer Therapeutic Target J Natl Cancer Inst. 2015 Dec 11;108(5)
To be eligible, you must have, or expect to achieve, at least a 2:1 honours degree or international equivalent. The studentship is open to home and EU candidates. If English is not your first language, you must have IELTS 7 with at least 6.5 in all the components.
How to apply
1. Speak to a prospective supervisor
Please email email@example.com to discuss the project further and get advice on completing the studentship form before applying through the University’s Doctoral College.
2. Complete the Doctoral College Studentships Award application
In addition to applying for a place on a postgraduate research course, you will also need to complete Doctoral College Studentships Award application form. This is your application for funding and will be used to select successful candidates for funding. Please also refer to the guidance notes which will assist you in filling in the application form. Once you have completed your form, please submit it to firstname.lastname@example.org.