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Peptide-Guided 
Theranostics

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The Peptide-Guided Theranostics lab aims to develop targeted therapies for hard-to-treat neoplasms like Glioblastoma, Neuroendocrine carcinoma and triple-negative breast cancer

About us

The goal of the Peptide-Guided Theranostics team is to identify targeting peptides that can guide therapies exclusively to the diseased tissue and thus reduce side effects. These targeting peptides are identified using an in vivo phage display screening technique where peptide libraries are expressed on bacteriophages.

 

The identified peptides are then synthesized and coupled to drugs or imaging agents and used in monovalent form, or coupled to nano-delivery systems (polymeric or lipid nanoparticles) that carry a drug or to contrast agents for diagnostic live imaging. In turn, identifying the binding partner of the peptide often unravels new molecular changes in the vasculature of the disease, thus identifying a new druggable target or biomarker.

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In this way, we have obtained targeting peptides for brain injuries, Alzheimer's Disease, Glioblastoma and Tumor-Associated Macrophages, which have given rise to 4 granted and licensed patents. One of those peptides, is being developed by the company Aivocode and is expected to enter clinical phases in 2026-2027. Peptides are already a large sector of the pharma industry; there are over 80 approved peptide-based drugs and in 2024 the second highest sales from the pharma industry was a peptide, proving this area of research is needed now most than ever.

Macrophage reprogramming

We aim to understand the role and biology of tumor associated macrophages (TAM) in solid tumors and develop tools to modulate them for therapeutic purposes. We developed a family of peptides to target tumor associated macrophages (TAM) in various solid tumors in mice: breast cancer, glioblastoma, melanoma, gastric cancer.

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“Combining neuroscience-inspired cancer therapies with emerging therapies that target cancer cell-intrinsic vulnerabilities and immunotherapies holds great therapeutic potential"
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SNAP25

We recently reported a new target in glioblastoma, the protein SNAP25. SNAP25 is part of the SNARE complex and is responsible for the fusion of vesicles (synaptic or hormone-containing) with the cell membrane, needed for exocytosis. SNAP25 is an intracellular protein in normal conditions, but in glioblastoma and neuroendocrine cancer we found that it becomes present on the cell surface and the vasculature.

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Pablo Scodeller

Principal Investigator

CSIC Tenured scientist

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Laura Tovar Martínez

Doctoral fellow

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Alberto G. Arias

Doctoral fellow

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Alberto López

Master's student

Affiliations

Dr. Pablo Scodeller is a CSIC tenured researcher in the Chemical Biology group at the Institute for Advanced Chemistry of Catalonia

Our group is part of the nanoDelivery strategic group of the Nanomedicine interdisciplinary network of the CSIC

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We are part of the Life Global area of the Spanish National Research Council

With support from:
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Cardiac Surgeon

Robert Griffith M.D

Practice Locations

Saint Francis Hospital

500 Terry Francine Street  

San Francisco, CA 94158

info@mysite.com

Tel: 123-456-7890

Fax: 123-456-7890

Private Clinic Info

500 Terry Francine Street  

San Francisco, CA 94158

info@mysite.com

Tel: 123-456-7890

Fax: 123-456-7890

© 2035 by Robert Griffith. Powered and secured by Wix

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