Show simple item record

dc.contributor.authorKarimi, N
dc.contributor.authorRashedi, J
dc.contributor.authorPoor, BM
dc.contributor.authorArabi, S
dc.contributor.authorGhorbani, M
dc.contributor.authorTahmasebpour, N
dc.contributor.authorAsgharzadeh, M
dc.date.accessioned2018-08-26T08:51:21Z
dc.date.available2018-08-26T08:51:21Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/53357
dc.description.abstractAim: The present study was conducted to survey the potential cytotoxic influence of freeze-dried aqueous extract of its fruits on gastrointestinal cell lines, namely AGS (human gastric carcinoma) and KYSE30 (human esophageal squamous cell carcinoma. Background: Rosemary (Rosmarinus officinalis) is a wild medicinal plant shown to have anticancer activity. Carnosic and rosmarinic acids are compounds, obtained from it through several extraction methods. Methods: The aqueous extract of the fruits of R.officinalis was freeze-dried, and KYSE30 and AGS cancer cell lines were treated with crude extract. Cytotoxic effect of the extracts on the cell lines was examined using 3-(4, 5-Dimethylthiazol-2-yl)-2, 5diphenyltetrazolium bromide (MTT) and neutral red assay. Apoptotic cells were detected with ethidium bromide/acridine orange (EB/AO). Cell-cycle distributions were evaluated by flow cytometry. Results: IC50 values were 4.1, 1.8 and 1.3 mg/mL for AGS cell lines after 24, 48 and 72 hours by MTT assay, respectively, and 4.4,2.1 and 1.1 mg/mL by neutral red assay, respectively. IC50 values for KYSE30 cell lines were 600, 180 and 150 mg/mL after 24, 48 and 72 hoursby MTT assay, and 860, 270 and 230 mg/mL by neutral red. EB/AO staining increased in apoptotic cells. After 24 hof treatment at different concentrations, significant increases and decreases in population were shown at G2/M and G1 phases, respectively. Conclusion: The aqueous extract of the fruits of R.officinalis was freeze-dried, and KYSE30 and AGS cancer cell lines were treated with crude extract. Cytotoxic effect of the extracts on the cell lines was examined using 3-(4, 5-Dimethylthiazol-2-yl)-2, 5diphenyltetrazolium bromide (MTT) and neutral red assay. Apoptotic cells were detected with ethidium bromide/acridine orange (EB/AO). Cell-cycle distributions were evaluated by flow cytometry. é 2017 RIGLD.
dc.language.isoEnglish
dc.relation.ispartofGastroenterology and Hepatology from Bed to Bench
dc.subjectacridine
dc.subjectethidium bromide
dc.subjectRosmarinus officinalis extract
dc.subjectwater
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcancer cell line
dc.subjectcell cycle
dc.subjectcell cycle G1 phase
dc.subjectcell viability
dc.subjectcontrolled study
dc.subjectcytotoxicity assay
dc.subjectdrug cytotoxicity
dc.subjectdrug effect
dc.subjectesophageal squamous cell carcinoma
dc.subjectflow cytometry
dc.subjectfruit
dc.subjectG2 phase cell cycle checkpoint
dc.subjecthuman
dc.subjecthuman cell
dc.subjectIC50
dc.subjectMTT assay
dc.subjectneutral red assay
dc.subjectstaining
dc.subjectstomach adenocarcinoma
dc.titleCytotoxic effect of rosemary extract on gastric adenocarcinoma (AGS) and esophageal squamous cell carcinoma (KYSE30) cell lines
dc.typeArticle
dc.citation.volume10
dc.citation.issue2
dc.citation.spage102
dc.citation.epage107
dc.citation.indexScopus


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record