Pregled bibliografske jedinice broj: 926458
GM3 and CD15s highly expressing breast cancer stem cells are sensitive to novel thieno[2, 3- b]pyridine anticancer compound treatment
GM3 and CD15s highly expressing breast cancer stem cells are sensitive to novel thieno[2, 3- b]pyridine anticancer compound treatment // Proceedings of the Second Adriatic Symposium on Biophysical Approaches in Biomedical Studies : book of abstracts / Raguž, Marija ; Kalyanaraman, Balaraman ; Sarna, Tadeusz (ur.).
Split: Medicinski fakultet Sveučilišta u Splitu, 2017. str. 65-65 (predavanje, međunarodna recenzija, sažetak, znanstveni)
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Naslov
GM3 and CD15s highly expressing breast cancer stem
cells are sensitive to novel thieno[2, 3-
b]pyridine anticancer compound treatment
Autori
Mastelić, Angela ; Marijan, Sandra ; Markotić, Anita ; Režić- Mužinić, Nikolina ; Vuica-Ross, Milena ; Benzon Benjamin ; Barker, David ; Reynisson, Johannes ; Čikeš- Čulić, Vedrana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Proceedings of the Second Adriatic Symposium on Biophysical Approaches in Biomedical Studies : book of abstracts
/ Raguž, Marija ; Kalyanaraman, Balaraman ; Sarna, Tadeusz - Split : Medicinski fakultet Sveučilišta u Splitu, 2017, 65-65
ISBN
978-953-7524-22-7
Skup
Second Adriatic Symposium on Biophysical Approaches in Biomedical Studies
Mjesto i datum
Split, Hrvatska, 24.09.2017. - 28.09.2017
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
breast cancer ; cancer stem cells ; GM3 ; CD15s
Sažetak
Small subpopulation of cancer stem cells (characterized by CD44+CD24− phenotype) expresses GM3(NeuAc) and CD15s glycoconjugates. Acidic glycosphingolipid GM3(NeuAc), containing neuraminic acid substituted with acetyl residue, is known to inhibit tyrosine kinase associated with fibroblast growth factor receptor. CD15s glycoconjugate is the major ligand of endothelial (E) selectin, responsible for cancer cell metastasizing. We performed preliminary studies of viability, and GM3(NeuAc) and CD15s expression after treatment of MDA-MB-231 triple-negative breast cancer cells with a newly developed thienopyridine anticancer compound (1). The MTT assay was used for the cellular metabolic activity determination. Cells expressing highly GM3(NeuAc) and CD15s were analysed for their CD44+CD24- subpopulation percentage, and GM3(NeuAc) and CD15s median fluorescence intensity in CD44+CD24- gate using flow cytometry. The percentages of highly expressing GM3(NeuAc) and CD15s cancer stem cells were lower, and their GM3(NeuAc) median fluorescence intensity was higher after treatment with compound 1 in comparison to non-treated cells. There was no difference in CD15s expression after treatment with the same compound. Knowing the inhibitory role of GM3(NeuAc) in fibroblast growth factor signal transduction, these findings render compound 1 potentially useful for triple- negative breast cancer treatment.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Split
Profili:
Sandra Marijan
(autor)
Benjamin Benzon
(autor)
Anita Markotić
(autor)
Angela Mastelić
(autor)
Vedrana Čikeš Čulić
(autor)
Nikolina Režić Mužinić
(autor)