2004
Quantitative assessment of the effects of chemicals on steroidogenic enzymes in the H295R cell line using real-time quantitative PCR
HILSCHEROVÁ, Klára; P.D. JONES; Tania GRACIA T; J.L. NEWSTED; X. ZHANG et. al.Základní údaje
Originální název
Quantitative assessment of the effects of chemicals on steroidogenic enzymes in the H295R cell line using real-time quantitative PCR
Název česky
Kvantitativní hodnocení účinků chemických látek na steroidogenní enzymy v buněčné linii H295R pomocí real-time PCR
Autoři
HILSCHEROVÁ, Klára; P.D. JONES; Tania GRACIA T; J.L. NEWSTED; X. ZHANG; J.T. SANDERSON; R. YU; R. WU a J.P. GIESY
Vydání
Toxicological sciences, 2004, 1096-6080
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: 3.391
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000223589100011
Klíčová slova česky
steroidogeneze; biotest; xenoestrogeny; skríning
Klíčová slova anglicky
Steroidogenesis; bioassay; xenoestrogens; screening
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 8. 4. 2009 16:37, doc. Mgr. Klára Hilscherová, Ph.D.
V originále
The potential for a variety of environmental contaminants to disturb endocrine function in wildlife species has been of recent concern. While much current effort is focused on the assessment of effects mediated through steroid hormone receptor based mechanisms, there is potentially a variety of other mechanisms, which could lead to endocrine disruption. Recent studies have demonstrated that a variety of xenobiotics can alter the gene expression or activity of enzymes involved in steroidogenesis. By altering the production of steroidogenic enzymes these chemicals have the potential to alter the delicate steroid balance in organisms. To assess the potential of chemicals to alter steroidogenesis an assay system was developed based on a human cell line that retains the ability to synthesize most of the important steroidogenic enzymes. Methods were developed to measure the expression of 10 genes involved in steroidogenesis by use of Q-RT-PCR. Assay conditions were optimized and expression levels were normalized to the expression of beta-actin. The effects of a variety of model chemicals known to alter steroid metabolism, both inducers and inhibitors, were assessed. Similar expression patterns were observed for chemicals acting through common mechanisms of action. Time-course studies demonstrated distinct time dependent expression profiles for chemicals able to modulate steroid metabolism. The assay, which allows simultaneous analysis of the expression of numerous steroidogenic enzymes, would be useful as a sensitive and rapid integrative screen for the many effects of chemicals on steroidogenesis.
Česky
Práce představuje nový model pro hodnocení ovlivnění steroidogeze xenobiotiky a metodu studia ovlivnění exprese steroidogeních enzymů pomocí real-time PCR.