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DynaCOMP

Assessing compounds targeting DNA replication licensing complexes as anti-tumor agents

Total Cost €

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EC-Contrib. €

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Partnership

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Project "DynaCOMP" data sheet

The following table provides information about the project.

Coordinator
PANEPISTIMIO PATRON 

Organization address
address: UNIVERSITY CAMPUS RIO PATRAS
city: RIO PATRAS
postcode: 265 04
website: www.upatras.gr

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 Greece [EL]
 Total cost 150˙000 €
 EC max contribution 150˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-PoC
 Funding Scheme ERC-POC
 Starting year 2017
 Duration (year-month-day) from 2017-07-01   to  2018-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    PANEPISTIMIO PATRON EL (RIO PATRAS) coordinator 150˙000.00

Map

 Project objective

Cancer is a major clinical, societal and economic burden worldwide and development of novel anti-cancer therapies constitutes a major investment of public and private funds. Despite intense research over decades however, which has led to a much improved understanding of cancer biology, cancer treatment remains a challenge. This is to a large extent due to the genetic heterogeneity of cancer and the ability of cancer cells to escape treatment by constantly undergoing further genetic alterations. During our ERC funded work, we have shown that aberrations in the DNA replication licensing pathway may contribute to the genome plasticity of cancer cells, and appear a common feature of cancer cells. They may however also constitute an Achilles foot, as cancer cells appear more dependent on negative regulators of the licensing system for survival. Cancer cells may therefore be more sensitive than normal cells to compounds targeting this control (inhibition of untimely licensing). We have identified compounds which target the DNA replication licensing inhibitor Geminin. The proposed PoC study will enable us to: - assess the efficacy and specificity of the identified compounds in cells and preclinical models and study their mechanism of action. - investigate the potential use of these compounds for studying cell cycle processes. - assess whether the functional imaging approaches developed under the mother ERC project, which quantify protein-protein interactions within living cells, may constitute a powerful tool for in-cell analysis of novel lead compounds. The project thus aims to characterize, protect and commercialize novel putative anti-tumor agents as well as the in-cell methods developed for their characterization.

 Publications

year authors and title journal last update
List of publications.
2018 Grigorios Koulouras, Andreas Panagopoulos, Maria A Rapsomaniki, Nickolaos N Giakoumakis, Stavros Taraviras, Zoi Lygerou
EasyFRAP-web: a web-based tool for the analysis of fluorescence recovery after photobleaching data
published pages: W467-W472, ISSN: 0305-1048, DOI: 10.1093/nar/gky508
Nucleic Acids Research 46/W1 2019-09-02
2018 Stella Maxouri, Stavros Taraviras, Zoi Lygerou
Visualizing the dynamics of histone variants in the S-phase nucleus
published pages: , ISSN: 1474-760X, DOI: 10.1186/s13059-018-1556-4
Genome Biology 19/1 2019-09-02
2018 Akiyo Hayashi, Nickolaos Nikiforos Giakoumakis, Tatjana Heidebrecht, Takashi Ishii, Andreas Panagopoulos, Christophe Caillat, Michiyo Takahara, Richard G Hibbert, Naohiro Suenaga, Magda Stadnik-Spiewak, Tatsuro Takahashi, Yasushi Shiomi, Stavros Taraviras, Eleonore von Castelmur, Zoi Lygerou, Anastassis Perrakis, Hideo Nishitani
Direct binding of Cdt2 to PCNA is important for targeting the CRL4 Cdt2 E3 ligase activity to Cdt1
published pages: e201800238, ISSN: 2575-1077, DOI: 10.26508/lsa.201800238
Life Science Alliance 1/6 2019-09-02

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