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THRON-SEC: Drug-Induced Secretome Profiling for Enhanced Therapy

Project description

Secretome profiling as a marker of drug efficacy

Medications can alter the secretome by influencing the types and amounts of proteins that cells release, reflecting changes in cellular metabolism, immune response or stress. These drug-induced changes in secreted proteins can provide important insights into the drug's efficacy, toxicity or potential to induce resistance, serving as early biomarkers for treatment outcomes. The ERC-funded THRON-SEC project aims to validate the technical and commercial feasibility of secretome profiling as a tool for assessing drug efficacy and safety. The study is based on a novel technique called THRONCAT that enables the identification and quantification of secreted proteins containing chemically modified analogues of the amino acid threonine.

Objective

Under normal conditions, cells release proteins (secretome) to regulate fundamental processes like metabolism and immunity. Many diseases and their corresponding treatments involve alterations in the secretome and the cellular microenvironment. Understanding drug-induced changes in the secretome is vital for early assessment of drug efficacy, toxicity, and resistance development. We have developed a metabolic protein labeling technique based on bioorthogonal threonine analogues, THRONCAT, that offers sensitive and non-perturbing analysis of drug-induced changes in the cellular secretome. THRONCAT enables the identification and quantification of secreted proteins in response to drug treatment, even in sensitive cellular systems. We envision that Drug-Induced Secretome Profiling (DISP), holds promise for improving clinical and preclinical drug development by detecting specific signaling proteins and biomarkers early in the development process and validated secreted proteins may serve as biomarkers to assess treatment efficacy during drug development and clinical trials. In this proof of concept proposal we will validate the technical and commercial feasibility of a platform that allows the analysis of the cellular secretome upon drug treatment. THRON-SEC will: 1) Show that secretome profiling upon drug treatment allows the elucidation of a drugs efficacy and mechanism of action as well as early detection of toxicity and resistance markers; and 2) Perform IPR, market and business case analyses to ensure commercial feasibility and entry to market.

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Topic(s)

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HORIZON-ERC-POC - HORIZON ERC Proof of Concept Grants

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Call for proposal

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(opens in new window) ERC-2024-POC

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Host institution

UNIVERSITEIT LEIDEN
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 150 000,00
Address
RAPENBURG 70
2311 EZ Leiden
Netherlands

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Activity type
Higher or Secondary Education Establishments
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Total cost

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Beneficiaries (1)

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