2013
Loss of the oligosaccharyl transferase subunit TUSC3 promotes proliferation and migration of ovarian cancer cells
VAŇHARA, Petr, Peter HORAK, Dietmar PILS, Mariam ANEES, Michaela PETZ et. al.Základní údaje
Originální název
Loss of the oligosaccharyl transferase subunit TUSC3 promotes proliferation and migration of ovarian cancer cells
Autoři
VAŇHARA, Petr (203 Česká republika, garant, domácí), Peter HORAK (40 Rakousko), Dietmar PILS (40 Rakousko), Mariam ANEES (40 Rakousko), Michaela PETZ (40 Rakousko), Wolfgang GREGOR (40 Rakousko), Robert ZEILLINGER (40 Rakousko) a Michael KRAINER (40 Rakousko)
Vydání
International Journal of Oncology, Athens, SPANDIDOS PUBL LTD, 2013, 1019-6439
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
Genetika a molekulární biologie
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.773
Kód RIV
RIV/00216224:14110/13:00081853
Organizační jednotka
Lékařská fakulta
UT WoS
000316511200030
Klíčová slova anglicky
TUSC3; ovarian cancer; glycosylation; proliferation
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 15. 6. 2015 12:19, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Consequences of deregulated protein N-glycosylation on cancer pathogenesis are poorly understood. TUSC3 is a gene with a putative function in N-glycosylation, located on the short arm of chromosome 8. This is a chromosomal region of frequent genetic loss in ovarian cancer. We established recently that the expression of TUSC3 is epigenetically decreased in epithelial ovarian cancer compared to benign controls and provides prognostic information on patient survival. Therefore, we analyzed the consequences of silenced TUSC3 expression on proliferation, invasion and migration of ovarian cell lines. In addition, we performed subcellular fractionation, co-immunofluorescence and co-immunoprecipitation experiments to establish the molecular localization of TUSC3 in ovarian cancer cells. We demonstrated that TUSC3 is localized in the endoplasmic reticulum as a subunit of the oligosaccharyltransferase complex and is capable of modulation of glycosylation patterning of ovarian cancer cells. Most importantly, silencing of TUSC3 enhances proliferation and migration of ovarian cancer cells in vitro. Our observations suggest a role for N-glycosylating events in ovarian cancer pathogenesis in general, and identify TUSC3 as a tumor suppressor gene in ovarian cancer in particular.
Návaznosti
EE2.3.20.0185, projekt VaV |
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7AMB12AT019, projekt VaV |
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