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Peptide-Drug Conjugates for Targeted Delivery in Tumor Therapy

Project
Many tumor cells are characterized by the overexpression of certain antigens. Molecules that specifically recognize these structures are suitable as homing devices in tumor therapy. Conjugates of anticancer drugs with such a delivery vector targeting tumors would be a ¿magic bullet¿ according to the Nobel laureate Paul Ehrlich. Three antibodydrug conjugates (ADC) have already been approved for anticancer therapy. However, ADC have e.g. limitations with respect to tumor penetration, high manufacturing costs, and require challenging conjugation chemistry. Peptide-drug conjugates can have a high drug loading, easily penetrate tissue, and can be easily prepared in a homogenous form with straightforward and well-defined conjugation chemistry. The ETN MAGICBULLET will focus on chemistry-driven approaches toward conjugates between peptides (delivery
vectors) that recognize tumors and anticancer drugs (payloads or warheads) in order to selectively fight cancer, a topic with a high demand of research activities. The ETN will develop and validate an array of new peptide-drug conjugates combining either known tumor-specific peptides or newly discovered tumor-homing peptides with potent cytotoxic drugs. The tumor-selective peptides are designed for cellular uptake mediated either by endocytosis or by cell-penetrating peptides. The consortium of the ETN MAGICBULLET covers tumor biology, biochemistry, pharmacology, synthetic chemistry, medicinal chemistry, spectroscopy, conformational analysis, and computational chemistry. The training program focuses on multidisciplinary research to explore and validate molecular targets for innovative treatment or investigations on the molecular mechanisms in organ-specific metastatic growth processes. It aims at scientific multilingualism and relies e.g. on concerted learning, a combination of introductory training, hands-on learning ¿on the bench¿, teaching by peers, and training in additional skills.
  • Overview
  • Publications

Overview

Departments involved

Dipartimento di Chimica   Principale  

Type

H20MCITNIF - Horizon 2020_Marie Skłodowska-Curie actions-Innovative Training Network (ITN)/Individual Fellowships (IF)

Funder

EUROPEAN COMMISSION
External Organization Funding Organization

Date/time interval

January 1, 2015 - December 31, 2018

Project duration

48 months

Publications

Outputs (7)

Conjugates of Cryptophycin and RGD or isoDGR Peptidomimetics for Targeted Drug Delivery 
CHEMISTRYOPEN
WILEY-VCH VERLAG GMBH & CO. KGAA, WEINHEIM
2019
Academic Article
Open Access
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Neutrophil Elastase Promotes Linker Cleavage and Paclitaxel Release from an Integrin-Targeted Conjugate 
CHEMISTRY-A EUROPEAN JOURNAL
WILEY BLACKWELL PUBLISHING
2019
Academic Article
Open Access
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Synthesis and Biological Evaluation of RGD and isoDGR-Monomethyl Auristatin Conjugates Targeting Integrin αVβ3 
CHEMMEDCHEM
WILEY-VCH
2019
Academic Article
Open Access
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β-Glucuronidase triggers extracellular MMAE release from an integrin-targeted conjugate 
ORGANIC & BIOMOLECULAR CHEMISTRY
ROYAL SOCIETY OF CHEMISTRY
2019
Academic Article
Partially Open Access
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Synthesis and biological evaluation of RGD and isoDGR peptidomimetic-α-amanitin conjugates for tumor-targeting 
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
BEILSTEIN-INSTITUT
2018
Academic Article
Open Access
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Multivalency Increases the Binding Strength of RGD Peptidomimetic-Paclitaxel Conjugates to Integrin αVβ3 
CHEMISTRY-A EUROPEAN JOURNAL
WILEY
2017
Academic Article
Open Access
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Tumor targeting with an isoDGR-Drug conjugate 
CHEMISTRY-A EUROPEAN JOURNAL
WILEY
2017
Academic Article
Open Access
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