2015
Ascites Increases Expression/Function of Multidrug Resistance Proteins in Ovarian Cancer Cells
LIHONG, M.o., Vendula POSPÍCHALOVÁ, Z.Q. HUANG, S.K. MURPHY, S. PAYNE et. al.Základní údaje
Originální název
Ascites Increases Expression/Function of Multidrug Resistance Proteins in Ovarian Cancer Cells
Autoři
LIHONG, M.o. (840 Spojené státy), Vendula POSPÍCHALOVÁ (840 Spojené státy, domácí), Z.Q. HUANG (840 Spojené státy), S.K. MURPHY (840 Spojené státy), S. PAYNE (840 Spojené státy), Fan WANG (840 Spojené státy, domácí), M. KENNEDY (840 Spojené státy), G.J. CIANCIOLO (840 Spojené státy), Vítězslav BRYJA (203 Česká republika, domácí), S.V. PIZZO (840 Spojené státy) a R.E. BACHELDER (840 Spojené státy)
Vydání
Plos one, San Francisco, Public Library of Science, 2015, 1932-6203
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30105 Physiology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.057
Kód RIV
RIV/00216224:14310/15:00084540
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000358157600111
Klíčová slova anglicky
CHEMOTHERAPY; SURVIVAL; GENE; TRANSPORTERS; KINASE; MDR1
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 5. 5. 2016 14:06, Ing. Andrea Mikešková
Anotace
V originále
Chemotherapy resistance is the major reason for the failure of ovarian cancer treatment. One mechanism behind chemo-resistance involves the upregulation of multidrug resistance (MDR) genes (ABC transporters) that effectively transport (efflux) drugs out of the tumor cells. As a common symptom in stage III/IV ovarian cancer patients, ascites is associated with cancer progression. However, whether ascites drives multidrug resistance in ovarian cancer cells awaits elucidation. Here, we demonstrate that when cultured with ascites derived from ovarian cancer-bearing mice, a murine ovarian cancer cell line became less sensitive to paclitaxel, a first line chemotherapeutic agent for ovarian cancer patients. Moreover, incubation of murine ovarian cancer cells in vitro with ascites drives efflux function in these cells. Functional studies show ascites-driven efflux is suppressible by specific inhibitors of either of two ABC transporters [Multidrug Related Protein (MRP1); Breast Cancer Related Protein (BCRP)]. To demonstrate relevance of our findings to ovarian cancer patients, we studied relative efflux in human ovarian cancer cells obtained from either patient ascites or from primary tumor. Immortalized cell lines developed from human ascites show increased susceptibility to efflux inhibitors (MRP1, BCRP) compared to a cell line derived from a primary ovarian cancer, suggesting an association between ascites and efflux function in human ovarian cancer. Efflux in ascites-derived human ovarian cancer cells is associated with increased expression of ABC transporters compared to that in primary tumor-derived human ovarian cancer cells. Collectively, our findings identify a novel activity for ascites in promoting ovarian cancer multidrug resistance.
Návaznosti
EE2.3.30.0009, projekt VaV |
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