2016
Co-expression of cancer stem cell markers corresponds to a pro-tumorigenic expression profile in pancreatic adenocarcinoma
ŠKODA, Jan, Markéta HERMANOVÁ, Tomáš LOJA, Pavel NĚMEC, Jakub NERADIL et. al.Základní údaje
Originální název
Co-expression of cancer stem cell markers corresponds to a pro-tumorigenic expression profile in pancreatic adenocarcinoma
Autoři
ŠKODA, Jan (203 Česká republika, domácí), Markéta HERMANOVÁ (203 Česká republika, domácí), Tomáš LOJA (703 Slovensko, domácí), Pavel NĚMEC (203 Česká republika, domácí), Jakub NERADIL (203 Česká republika, domácí), Petr KARÁSEK (203 Česká republika) a Renata VESELSKÁ (203 Česká republika, garant, domácí)
Vydání
PLOS One, San Francisco, PUBLIC LIBRARY SCIENCE, 2016, 1932-6203
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.806
Kód RIV
RIV/00216224:14310/16:00095874
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000379579500112
Klíčová slova anglicky
pancreatic adenocarcinoma;cancer stem cell markers;expression profilimg
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 1. 11. 2019 14:34, Mgr. Michal Petr
Anotace
V originále
Pancreatic ductal adenocarcinoma (PDAC) remains one of the most lethal malignancies. Its dismal prognosis is often attributed to the presence of cancer stem cells (CSCs) that have been identified in PDAC using various markers. However, the co-expression of all of these markers has not yet been evaluated. Furthermore, studies that compare the expression levels of CSC markers in PDAC tumor samples and in cell lines derived directly from those tumors are lacking. Here, we analyzed the expression of putative CSC markers-CD24, CD44, epithelial cell adhesion molecule (EpCAM), CD133, and nestin-by immunofluorescence, flow cytometry and quantitative PCR in 3 PDAC-derived cell lines and by immunohistochemistry in 3 corresponding tumor samples. We showed high expression of the examined CSC markers among all of the cell lines and tumor samples, with the exception of CD24 and CD44, which were enriched under in vitro conditions compared with tumor tissues. The proportions of cells positive for the remaining markers were comparable to those detected in the corresponding tumors. Co-expression analysis using flow cytometry revealed that CD24+/CD44+/EpCAM+/CD133+ cells represented a significant population of the cells (range, 43 to 72%) among the cell lines. The highest proportion of CD24+/CD44+/EpCAM+/CD133+ cells was detected in the cell line derived from the tumor of a patient with the shortest survival. Using gene expression profiling, we further identified the specific pro-tumorigenic expression profile of this cell line compared with the profiles of the other two cell lines. Together, CD24+/CD44+/EpCAM+/CD133+ cells are present in PDAC cell lines derived from primary tumors, and their increased proportion corresponds with a pro-tumorigenic gene expression profile.
Návaznosti
EE2.3.20.0183, projekt VaV |
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