Cytotoxicity, apoptosis inducing activity and Western blot analysis of tanshinone derivatives from Stachys parviflora on prostate and breast cancer cells.
Abolfazl ShakeriToktam HafezianNorbert KúszJudit HohmannMotahare BoozariJavad MottaghipishehSeyed Ahmad EmamiZahra Tayarani-NajaranJavad AsiliPublished in: Molecular biology reports (2022)
Cytotoxic activities of methanolic crude extract of Stachys parviflora (Lamiaceae family) and its sub-fractions were primarily evaluated against human breast adenocarcinoma (MCF-7 and MDA-MB-231) and prostate (PC3) cell lines. The methanolic extract exhibited the highest activity, and was chosen for the isolation procedure. Four diterpenoid quinones, namely miltirone [1], tanshinone IIA [2], 1-hydroxy-tanshinone IIA [3], and cryptotanshinone [4] were isolated. Notably, this is the first report on the isolation and/or characterization of the mentioned diterpenoids from the Stachys genus. In this study, 1-hydroxy-tanshinone IIA [3] displayed the highest cytotoxicity among the isolated compounds. The mechanism of the cytotoxicity of methanolic extract and isolated compounds was further investigated by the utilization of propidium iodide staining (PI) assay. The results showed that the methanolic extract and 1-hydroxy-tanshinone IIA [3] enhanced DNA fragmentation in PC3 and MCF-7 cells. Moreover, the western blotting analysis demonstrated increasing and decreasing protein levels of Bax and Bcl2, respectively, and cleaved poly ADP-ribose polymerase (PARP). Further bioassay-guided phytochemical assessments of S. parviflora can be suggested as a promising approach for discovering potent bioactive secondary metabolites.
Keyphrases
- breast cancer cells
- oxidative stress
- cell cycle arrest
- induced apoptosis
- prostate cancer
- anti inflammatory
- endothelial cells
- cell death
- endoplasmic reticulum stress
- dna damage
- south africa
- benign prostatic hyperplasia
- high throughput
- dna repair
- pi k akt
- minimally invasive
- binding protein
- cell free
- induced pluripotent stem cells
- data analysis