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STARFISH DNA

Stalling the Replication Fork via the Impedimental Stabilization of Higher-order DNAs

Total Cost €

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EC-Contrib. €

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Partnership

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Project "STARFISH DNA" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITE DIJON BOURGOGNE 

Organization address
address: ESPLANADE ERASME MAISON DE L UNIVERSITE
city: DIJON CEDEX
postcode: 21078
website: www.u-bourgogne.fr

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country France [FR]
 Project website https://sites.google.com/site/monchaudchembiolab/starfish-dna
 Total cost 185˙076 €
 EC max contribution 185˙076 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-10-01   to  2019-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITE DIJON BOURGOGNE FR (DIJON CEDEX) coordinator 185˙076.00

Map

 Project objective

'Cancer is a generic term for a group of diseases characterized by the uncontrolled growth and spread of cells with abnormal proliferating activity. Most of the anticancer drugs currently used in the clinic trigger irreversible DNA damages and thus, promote replicative stress. As an alternative of irreversible DNA strand breaks, the non-covalent small-molecule stabilization of unusual, non-B DNA structures has emerged as a promising way to create DNA damages. One of such non B-DNA structures is a three-way DNA junction that might fold both upstream and downstream of the replication fork. The stabilization of three-way junctions by small molecules therefore opens a promising way to induce replicative stress in a highly cancer-specific manner. The main goal of the project 'STARFISH DNA' (for 'Stalling the Replication Fork via the Impedimental Stabilization of Higher-order DNAs') is to identify a new series of compounds capable of creating DNA damages through three-way junction stabilization and to use them either as standalone therapeutic agent to fight against cancers or in combination with established drugs that disrupt cancer signaling pathways in a synergistic manner.'

 Publications

year authors and title journal last update
List of publications.
2019 Pauline Lejault, Katerina Duskova, Claire Bernhard, Ibai E. Valverde, Anthony Romieu, David Monchaud
The Scope of Application of Macrocyclic Polyamines Beyond Metal Chelation
published pages: 6146-6157, ISSN: 1434-193X, DOI: 10.1002/ejoc.201900870
European Journal of Organic Chemistry 2019/36 2020-03-23
2019 Katerina Duskova, Jérémy Lamarche, Souheila Amor, Coralie Caron, Nicolas Queyriaux, Marie Gaschard, Marie-José Penouilh, Guillaume de Robillard, Dominique Delmas, Charles H. Devillers, Anton Granzhan, Marie-Paule Teulade-Fichou, Murielle Chavarot-Kerlidou, Bruno Therrien, Sébastien Britton, David Monchaud
Identification of Three-Way DNA Junction Ligands through Screening of Chemical Libraries and Validation by Complementary in Vitro Assays
published pages: 4456-4466, ISSN: 0022-2623, DOI: 10.1021/acs.jmedchem.8b01978
Journal of Medicinal Chemistry 62/9 2020-03-23
2017 Ludivine Guyon, Marc Pirrotta, Katerina Duskova, Anton Granzhan, Marie-Paule Teulade-Fichou, David Monchaud
TWJ-Screen: an isothermal screening assay to assess ligand/DNA junction interactions in vitro
published pages: , ISSN: 0305-1048, DOI: 10.1093/nar/gkx1118
Nucleic Acids Research 2020-03-23

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The information about "STARFISH DNA" are provided by the European Opendata Portal: CORDIS opendata.

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