Pregled bibliografske jedinice broj: 809217
Comparison of antitumor activity of some benzothiophene, thienothiophene, carboxanilides and quinolones in 2D and 3D cell culture system
Comparison of antitumor activity of some benzothiophene, thienothiophene, carboxanilides and quinolones in 2D and 3D cell culture system // EMBO/EMBL Symposium: Tumour microenviroment and signaling / carolina Garcia Sabate (ur.).
Heidelberg: EMBL Heidelberg Germany, 2016. str. 83-83 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 809217 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Comparison of antitumor activity of some benzothiophene, thienothiophene, carboxanilides and quinolones in 2D and 3D cell culture system
Autori
Zlatar, Ivo ; Hranjec, Marijana ; Jelić, Dubravko ; Cindrić, Maja ; Jarak, Ivana ; Karminski-Zamola, Grace ; Brajša, Karmen
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
EMBO/EMBL Symposium: Tumour microenviroment and signaling
/ Carolina Garcia Sabate - Heidelberg : EMBL Heidelberg Germany, 2016, 83-83
Skup
EMBO/EMBL Symposium: Tumour microenviroment and signaling
Mjesto i datum
Heidelberg, Njemačka, 03.04.2016. - 06.04.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
antitumor activity; benzothiophenes; carboxanilides; thienothiophenes; quinolones; 2D and 3D in vitro assay
Sažetak
One of the main reasons of high drug attrition rate in oncology is poor clinical predictive power of 2D cell cultures that are historically used as a standard tool for in vitro assays as an integral part of drug discovery process. For this reason, there is increasing interest in developing 3D in vitro cell culture systems which represent a biologically relevant assay system, feasible for the development of robust preclinical anti-cancer drug screening platforms. Over the past few years substituted heterocyclic derivatives have been one of the most extensively studied classes of organic compounds due to their well known biological activities. Substituted heterocyclic quinolones and carboxamides exhibit several pharmacological activities and have therefore attracted considerable attention from medicinal and synthetic organic chemists. As a part of our continuing search for potential anticancer agents related to heterocyclic quinolones, we have previously reported synthesis and strong inhibitory activities on several human tumour cell lines of versatile benzothiophene and thienothiophene carboxanilides and quinolones (Fig. 1) thus confirming the anticancer potential of this class of compounds [1]. In addition, 3D hanging-drop cell culture method was applied on a human cancer breast cell lines (SK-BR-3, MDA-MB-231, T-47D) and their antitumor activity in vitro ion 2D cell culture was compared with activity of 3D cell culture system. Obtained results in some cases showed significant disagreement indicating that some prominent compounds can be discarded in early phase of researching while chance was given to compounds with false positive result.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
125-0982464-1356 - Novi heterocikli kao antitumorski i antivirusni (pametni) lijekovi (Hranjec, Marijana, MZOS ) ( CroRIS)
Ustanove:
Fidelta d.o.o.
Profili:
Ivana Jarak
(autor)
Grace Karminski-Zamola
(autor)
Dubravko Jelić
(autor)
Karmen Brajša
(autor)
Marijana Hranjec
(autor)
Maja Cindrić
(autor)