[INFLUENCE OF PROGESTERONE DERIVATIVES ON THE VIABILITY AND EXPRESSION OF ESTROGEN RECEPTOR-ALPHA MRNA IN HELA CELLS]

Eksp Klin Farmakol. 2016;79(9):22-24.
[Article in Russian]

Abstract

We have studied the effect of new ligands of progesterone receptors, including pregna-D'-pentaran 6-methoxyimino-16a,17a-cyclohexanopregn-4-en-3,20-dio-ne (K1047), 17a-acetoxy-3b-butanoyloxy-6-methylpregna-4,6-dien-20-one (buterol), progesterone (P4), and medroxyprogesterone acetate on the viability of HeLa cells and expression of estrogen receptor-alpha (Era) mRNA gene in these cells. K1I047 and buterol exhibited high cytostatic activity, which exceeded the activity of reference compounds on the average by 15% (p < 0.05). Both buterol and K-1047 (at 10(-6)M) effectively suppressed ERa mRNA gene expression in HeLa cell culture by 83.4 - 9 8.6%.

MeSH terms

  • Cell Survival / drug effects
  • Estrogen Receptor alpha / biosynthesis*
  • Gene Expression Regulation / drug effects*
  • HeLa Cells
  • Humans
  • Progesterone* / analogs & derivatives
  • Progesterone* / pharmacology

Substances

  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Progesterone