Back to Search
Start Over
In vitro antiproliferative effect of six salvia species on human tumor cell lines
- Publication Year :
- 2006
-
Abstract
- This study was designed to examine the in vitro antiproliferative activity of the methanol crude extracts of six Salvia species: Salvia dominica L. leaves, Salvia lanigera Desf. aerial parts, Salvia menthaefolia Ten. roots, Salvia palaestina Benth. aerial parts, Salvia sclarea L. roots and Salvia spinosa L. aerial parts. Extracts were screened for their possible antitumoral activity by MTT test on nine human cancer cell lines: glioblastoma (DBTRG-05MG, T98G, U-87MG), colorectal adenocarcinoma (WiDr and HT-29), prostate adenocarcinoma (MDA Pca2b), choriocarcinoma (JEG-3), endometrium adenocarcinoma (HEC-1A) and B lymphoblast (CIR). IC50 values were determined for only five extracts and ranged from 90 to 400 mg/mL approximately. Salvia menthaefolia extract exhibited marked antiproliferative activity against all tumor cell lines showing lower IC50 values, while S. spinosa, S. sclarea and S. dominica extracts showed a degree cytotoxic activity dependent on the cell line type. Finally S. palaestina extract revealed a moderate antiproliferative effect only against three cell lines. Salvia lanigera extract displayed toxic activity at all concentrations tested. The results strengthen the evidence that the genus Salvia could be considered a natural resource of potential antitumor agents. Copyright © 2006 John Wiley & Sons, Ltd.
- Subjects :
- extracts
Cell Survival
Salvia species
antitumoral activity
cell lines
toxicity
Antineoplastic Agents
Pharmacognosy
Salvia
Inhibitory Concentration 50
Cell Line, Tumor
Botany
medicine
Humans
Salvia sclarea
Salvia lanigera
Cell Proliferation
Pharmacology
Dose-Response Relationship, Drug
biology
Traditional medicine
Plant Extracts
Salvia palaestina
medicine.disease
biology.organism_classification
Cell culture
Adenocarcinoma
Drug Screening Assays, Antitumor
Salvia dominica
Phytotherapy
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....9bd078dfe035c1edfb055d9e78425f18