Pin1 Degradation as Therapeutic Approach to Multiple Myeloma
ABG-131671 | Thesis topic | |
2025-05-05 | Public/private mixed funding |
- Chemistry
- Biology
Topic description
Context and Project Objectives: Multiple Myeloma (MM), a haematological malignancy of plasma cells, remains largely incurable due to persistent drug resistance and disease relapse, highlighting the urgent need for innovative therapeutic targets and strategies. Pin1, a small protein belonging to the Peptidyl-Prolyl cis-trans Isomerase family, has emerged as a pivotal oncoprotein implicated in the pathogenesis of various tumours. Recent studies emphasise Pin1's critical role in driving resistant MM progression. Despite its compelling oncogenic role, Pin1’s small and shallow enzymatic pocket pose significant challenges for conventional drug design, limiting the development of effective inhibitors. To overcome these obstacles, we propose a paradigm shift: harnessing the power of Targeted Protein Degradation (TPD). This innovative approach, which has revolutionised chemical biology and drug discovery in recent years, offers a promising strategy to therapeutically target previously “undruggable” proteins such as Pin1. This project aims to develop Pin1 degraders to selectively eliminate this protein, addressing both drug resistance and disease relapse in MM. In addition, Pin1 degraders will serve as valuable tools to further investigate the role of Pin1 in MM progression and the emergence of drug resistance.
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Funding further details
Presentation of host institution and host laboratory
BioCIS (UMR CNRS 8076)
Team of Chemical Biology
Since January 2020, the Chemical Biology Team of CY Cergy Paris Université has joined the UMR CNRS BioCIS (Biomolecules: Design, Isolation, Synthesis) of the Faculty of Pharmacy of the University of Paris Saclay. The Chemical Biology team is located on the university site of Neuville/Oise. The team brings together researchers on the general theme of chemistry oriented towards the life sciences. We study the synthesis, characterization and evaluation of biomolecules, as well as the development of new synthetic methodologies.
We are specialized in the chemistry of modified amino acids and in particular fluorinated peptides, glycosides, glycopeptides, for applications in the field of biological chemistry and medicinal chemistry.
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Institution awarding doctoral degree
Candidate's profile
Job Description: This is an innovative and challenging interdisciplinary project in which the PhD student will be responsible for both the synthetic work and the biological evaluation of the final degraders. It represents an excellent opportunity for the successful candidate to build a strong foundation in organic chemistry applied to drug discovery, while also acquiring critical interdisciplinary skills in chemical biology and medicinal chemistry. The student will benefit from a stimulating research environment within a young and dynamic Team with diverse international backgrounds and strong expertise in the design and development of bioactive molecules and chemical biology. The PhD position will be based at the BioCIS laboratory (FR), but the project is conducted in collaboration with several European academic partners: Innsbruck Medical University (Austria), Sorbonne Université (France), Vrije Universiteit Brussel (Belgium), and Université de Strasbourg (France). The student will be expected to interact closely with these partners and follow the progress of the collaborative work.
Candidate’s Requirements: The ideal candidate should be highly motivated to work at the interface between chemistry and biology. A Master's degree in Chemistry (or an equivalent qualification) is required, along with strong theoretical and practical knowledge in organic synthesis and in the characterisation of organic compounds. Prior experience in chemical biology will be considered an asset. A good level of English is essential for bibliographical research and interaction within our European research team.
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