Back to Search Start Over

Cytotoxic Potential of Rare Plant Salvia candidissima subsp. candidissima on Breast Cancer Cells

Authors :
Erturk, Elif
Onur, Omer Enes
Aydin, Ipek
Ozel, Mustafa Zafer
Firat, Mehmet
Ari, Ferda
Source :
Brazilian Archives of Biology and Technology, Volume: 66, Article number: e23220358, Published: 19 JUN 2023
Publication Year :
2023
Publisher :
Instituto de Tecnologia do ParanĂ¡ - Tecpar, 2023.

Abstract

Breast cancer is the leading cause of cancer-related deaths in women throughout the world. Research on natural anti-cancer products from plants has gained traction. Salvia L. species and their derivatives are rare in Turkey and have suggested for their potential anti-cancer effects. The aim of this study is to assess the potential cytotoxic/apoptotic activities of methanol extract of Salvia candidissima Vahl. subsp. candidissima (SCE) on MCF-7 and MDA-MB-231 breast cancer cells. A GCxGC-TOF/MS system and a dual stage commercial thermal desorption injector were used to determine the chemical components of SCE. MTT and ATP viability tests were used to investigate the anti-growth activity. The apoptosis-inducing effect was assessed using a fluorescence staining method. Caspase-cleaved keratin 18 (ccK18, M30-antigen) levels measured by M30-CytoDeath ELISA Kit. The results showed that SCE suppressed the survival of the MCF-7 and MDA-MB-231 breast cancer cells in a dose-dependent manner, based on the findings of both MTT and ATP cell viability tests and pyknotic cell nuclei were observed via fluorescent staining in both cell lines after 48 h of treatment. The treatment group had greater levels of caspase-cleaved keratin 18 in the MCF-7 cells than the untreated group. These results showed that SCE triggers apoptosis, causes cell death in MCF-7 and MDA-MB-231 cell lines. SCE may become promising therapeutic strategy in the treatment of breast cancer with further in vitro and in vivo studies.

Details

Language :
English
Database :
OpenAIRE
Journal :
Brazilian Archives of Biology and Technology, Volume: 66, Article number: e23220358, Published: 19 JUN 2023
Accession number :
edsair.od.......608..72e671d62d7b66fe2ecd09279a4fd50c