Detailed Information on Publication Record
2020
Specific alterations of sphingolipid metabolism identified in EpCAM-positive cells isolated from human colon tumors
PROCHAZKOVA, Jirina, Josef SLAVIK, Jan BOUCHAL, Monika LEVKOVA, Zlata HUSKOVA et. al.Basic information
Original name
Specific alterations of sphingolipid metabolism identified in EpCAM-positive cells isolated from human colon tumors
Authors
PROCHAZKOVA, Jirina (203 Czech Republic), Josef SLAVIK (203 Czech Republic), Jan BOUCHAL (203 Czech Republic), Monika LEVKOVA (203 Czech Republic), Zlata HUSKOVA (203 Czech Republic), Jiri EHRMANN (203 Czech Republic), Petra OVESNÁ (203 Czech Republic, belonging to the institution), Zdenek KOLAR (203 Czech Republic), Pavel SKALICKY (203 Czech Republic), Nicol STRAKOVA (203 Czech Republic), Ondrej ZAPLETAL (203 Czech Republic), Alois KOZUBIK (203 Czech Republic), Jirina HOFMANOVA (203 Czech Republic), Jan VONDRACEK (203 Czech Republic) and Miroslav MACHALA (203 Czech Republic, guarantor)
Edition
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, AMSTERDAM, ELSEVIER, 2020, 1388-1981
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.698
RIV identification code
RIV/00216224:14110/20:00116195
Organization unit
Faculty of Medicine
UT WoS
000552710900012
Keywords in English
Sphingolipid metabolism; Colon adenocarcinoma; Lactosylceramide; B4GALTs; EPCAM-positive cells
Tags
International impact, Reviewed
Změněno: 13/8/2020 08:32, Mgr. Tereza Miškechová
Abstract
V originále
Metabolic reprogramming leading to alterations in lipid metabolism and lipid-mediated signaling may contribute to colorectal cancer (CRC) development and progression. We hypothesized that a detailed description of changes in sphingolipidome of specific cellular subpopulation residing in colon cancer tissue may help to discriminate between normal and transformed colon epithelial cells. Using HPLC-mass spectrometry, we analyzed the EpCAM-positive cells isolated from tumor and adjacent non-tumor tissues of colon cancer patients, aiming to identify potential lipid biomarkers specific for CRC. We then employed RT-qPCR-based methodology in order to analyze expression of SL metabolism-related genes in the isolated EpCAM-positive tumor cells and/or in unseparated colon tumor tissues. We observed significant changes in sphingolipid (SL) species in the EpCAM-positive tumor cells, with the accumulation of lactosylceramide (LacCer) being the most prominent. B4GALT5 and B4GALT6 genes were identified as two potential gene candidates contributing to LacCer accumulation. We further identified additional genes of SL and fatty acid metabolism (e.g. SPHK1, GBA2, NEU3, GLA, FASN, PLA2G10), which were significantly altered in colon tumor tissue. The present results indicate that the EpCAM-positive cells are a major contributor to LacCer accumulation in CRC tissue, and may help to identify novel CRC-specific lipid/gene biomarkers.