A high-throughput screening of a chemical compound library in ovarian cancer stem cells

Background: Epithelial ovarian cancer has a poor prognosis, mostly due to its late diagnosis and the development of drug resistance after a first platinum-based regimen. The presence of a specific population of "cancer stem cells" could be responsible of the relapse of the tumor and the de...

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Ricci F.
Carrassa L.
Christodoulou M. S.
Passarella D.
Michel B.
Hunyadi Attila
Botta B.
Kavetsou E.
Detsi A.
Majer Zsuzsanna (Deckerné)
Hudecz Ferenc
Bősze Szilvia
Kaminska B.
Hansen T. V.
Bertrand P.
Dokumentumtípus: Cikk
Megjelent: 2018
Sorozat:COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 21 No. 1
doi:10.2174/1386207321666180124093406

mtmt:3356960
Online Access:http://publicatio.bibl.u-szeged.hu/13794
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490 0 |a COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING  |v 21 No. 1 
520 3 |a Background: Epithelial ovarian cancer has a poor prognosis, mostly due to its late diagnosis and the development of drug resistance after a first platinum-based regimen. The presence of a specific population of "cancer stem cells" could be responsible of the relapse of the tumor and the development of resistance to therapy. For this reason, it would be important to specifically target this subpopulation of tumor cells in order to increase the response to therapy. Method: We screened a chemical compound library assembled during the COST CM1106 action to search for compound classes active in targeting ovarian stem cells. We here report the results of the high-throughput screening assay in two ovarian cancer stem cells and the differentiated cells derived from them. Results and Conclusion: Interestingly, there were compounds active only on stem cells, only on differentiated cells, and compounds active on both cell populations. Even if these data need to be validated in ad hoc dose response cytotoxic experiments, the ongoing analysis of the compound structures will open up to mechanistic drug studies to select compounds able to improve the prognosis of ovarian cancer patients. 
700 0 1 |a Carrassa L.  |e aut 
700 0 1 |a Christodoulou M. S.  |e aut 
700 0 1 |a Passarella D.  |e aut 
700 0 1 |a Michel B.  |e aut 
700 0 1 |a Hunyadi Attila  |e aut 
700 0 1 |a Botta B.  |e aut 
700 0 1 |a Kavetsou E.  |e aut 
700 0 1 |a Detsi A.  |e aut 
700 0 1 |a Majer Zsuzsanna (Deckerné)  |e aut 
700 0 1 |a Hudecz Ferenc  |e aut 
700 0 1 |a Bősze Szilvia  |e aut 
700 0 1 |a Kaminska B.  |e aut 
700 0 1 |a Hansen T. V.  |e aut 
700 0 1 |a Bertrand P.  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/13794/1/ricci2018.pdf  |z Dokumentum-elérés