J 2015

17 beta-estradiol-containing liposomes as a novel delivery system for the antisense therapy of ER-positive breast cancer: An in vitro study on the MCF-7 cell line

HEGER, Zbynek, Jaromír GUMULEC, Natalia CERNEI, Katerina TMEJOVA, Pavel KOPEL et. al.

Základní údaje

Originální název

17 beta-estradiol-containing liposomes as a novel delivery system for the antisense therapy of ER-positive breast cancer: An in vitro study on the MCF-7 cell line

Autoři

HEGER, Zbynek (203 Česká republika), Jaromír GUMULEC (203 Česká republika, domácí), Natalia CERNEI (498 Moldavsko), Katerina TMEJOVA (203 Česká republika), Pavel KOPEL (203 Česká republika), Jan BALVAN (203 Česká republika, domácí), Michal MASAŘÍK (203 Česká republika, garant, domácí), Ondrej ZITKA (203 Česká republika), Miroslava BEKLOVA (203 Česká republika), Vojtech ADAM (203 Česká republika) a Rene KIZEK (203 Česká republika)

Vydání

Oncology Reports, Athens, Spandidos Publications, 2015, 1021-335X

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30200 3.2 Clinical medicine

Stát vydavatele

Řecko

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 2.486

Kód RIV

RIV/00216224:14110/15:00083937

Organizační jednotka

Lékařská fakulta

UT WoS

000348338500054

Klíčová slova anglicky

antisense therapy; delivery; glutathione; liposome; malondialdehyde; metallothionein

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 22. 9. 2015 15:46, Soňa Böhmová

Anotace

V originále

The present study suggests and describes the application of a delivery system for antisense oligonucleotides against mRNA encoding estrogen receptor proteins alpha and beta. The delivery system is composed of a cationic liposome envelope containing 17 beta-estradiol (E-2) in its structure. Cationic liposomes protect cargo against the extracellular matrix, and E-2 can increase its shuttling efficiency into cells. Using MCF-7 cells derived from estrogen receptor-positive ductal carcinoma, treatment with liposomes against ER alpha was found to decrease MCF-7 proliferation, and importantly the application of both the antisense against ER alpha and beta exhibited an antiproliferative effect expressed as cell viability. Using qRT-PCR, it was shown that MTIA,NF-kappa B1 and K-ras genes, but not TFF1, were downregulated using E-2-based liposomes (evaluated at P=0.05). Further indicators of oxidative stress were employed to assess the effect on treatment efficiency. Glutathione (GSH/GSSG redox ratio), metallothionein (MT) and malondialdehyde (MDA) confirmed a positive effect of antisense therapy resulting in their decreased levels in the MCF-7 cells. Based on these data, we suggest that E2-based liposomes offer sufficient transfer efficiency and moreover, due to the effect on NF-kappa BI, MT and GSH, tumor cells can be chemosensitized to increase treatment effectiveness.

Návaznosti

ED1.1.00/02.0068, projekt VaV
Název: CEITEC - central european institute of technology