Detailed Information on Publication Record
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.Basic information
Original name
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
Authors
HEGER, Zbynek (203 Czech Republic), Jaromír GUMULEC (203 Czech Republic, belonging to the institution), Natalia CERNEI (498 Republic of Moldova), Katerina TMEJOVA (203 Czech Republic), Pavel KOPEL (203 Czech Republic), Jan BALVAN (203 Czech Republic, belonging to the institution), Michal MASAŘÍK (203 Czech Republic, guarantor, belonging to the institution), Ondrej ZITKA (203 Czech Republic), Miroslava BEKLOVA (203 Czech Republic), Vojtech ADAM (203 Czech Republic) and Rene KIZEK (203 Czech Republic)
Edition
Oncology Reports, Athens, Spandidos Publications, 2015, 1021-335X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
Greece
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.486
RIV identification code
RIV/00216224:14110/15:00083937
Organization unit
Faculty of Medicine
UT WoS
000348338500054
Keywords in English
antisense therapy; delivery; glutathione; liposome; malondialdehyde; metallothionein
Tags
Tags
International impact, Reviewed
Změněno: 22/9/2015 15:46, Soňa Böhmová
Abstract
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.
Links
ED1.1.00/02.0068, research and development project |
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