Inhibition of human glioma cell proliferation by altered Bax/Bcl-2-p53 expression and apoptosis induction by Rhaponticum carthamoides extracts from transformed and normal roots

Ewa Skała, Przemysław Sitarek, Monika Toma, Janusz Szemraj, Maciej Radek, Malgorzata Nieborowska-Skorska, Tomasz Skorski, Halina Wysokińska, Tomasz Śliwiński

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

Objective: The objective of this study was to determine the cytotoxic effect and apoptotic activity of Rhaponticum carthamoides transformed root (TR) and root of soil-grown plant (NR) extracts in a human glioma primary cells. The effect of these root extracts on cell cycle arrest, mitochondrial membrane potential (ΔΨm) and expression levels of apoptosis-related genes (Bcl-2, Bax and p53) were also examined. Methods: Cytotoxic activity of root extracts was evaluated by MTT assay. Apoptosis and cell cycle were determined by flow cytometry. Expression levels of apoptosis-related gene were analysed by RT-PCR and Western blotting. ΔΨm was examined by the use of JC-1 reagent. Key findings: Rhaponticum carthamoides root extracts inhibit cell growth and induce apoptosis in a dose-dependent manner in human glioma cells. The root extracts were found to up-regulate the pro-apoptotic Bax protein and down-regulate the anti-apoptotic Bcl-2 protein, consequently increasing the ratios of Bax/Bcl-2 protein levels. Moreover, an increase of the p53 protein level and reduction of ΔΨm in glioma cells were observed after treatment with NR and TR extracts. Conclusion: The results of this study may offer a new insight into the potential anticancer activity of R. carthamoides root extracts.

Original languageEnglish
Pages (from-to)1454-1464
Number of pages11
JournalJournal of Pharmacy and Pharmacology
Volume68
Issue number11
DOIs
StatePublished - Nov 1 2016
Externally publishedYes

Keywords

  • Bax
  • Bcl-2 and p53 gene expressions
  • Rhaponticum carthamoides
  • apoptosis
  • caffeic acid derivatives
  • glioma primary cells
  • mitochondrial membrane potential

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