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Determination of anti-cancer effects of Nigella sativa seed oil on MCF7 breast and AGS gastric cancer cells

dc.contributor.authorÇınar, İrfan
dc.contributor.authorGıdık, Betül
dc.contributor.authorDirican, Ebubekir
dc.date.accessioned2026-01-04T20:17:58Z
dc.date.issued2024-04-05
dc.description.abstractThis study aimed to investigate the cytotoxic, apoptotic, invasion, metastasis, and heat shock proteins (HSPs) effects of N. sativa oil on breast and gastric cancer cells.We assessed the cytotoxic and apoptotic effects of various concentrations of N. sativa oil (10-50-100-200 µg/mL) on MCF7 breast cancer and AGS, an adenocarcinoma of the gastric cell line, at 24, 48 and 72 h using the MTT test. Additionally, the expression of the Caspase-3, BCL2/Bax, MMP2-9 and HSP60-70 gene was examined using RT-PCR in cell lines treating with N. sativa.The MTT experiments demonstrate that N. sativa has a time and dose-dependent inhibitory effect on the proliferation of MCF7 and AGS cancer cells. The vitality rates of MCF7 and AGS cells treated with N. sativa were 77.04-67.50% at 24 h, 65.28-39.14% at 48 h, and 48.95-32.31% at 72 h. The doses of 100 and 200 µg/mL were shown to be the most effective on both cancer cells. RT-PCR analysis revealed that N. sativa oil extract increased caspase-3 levels in both cell lines at higher concentrations and suppressed BCL2/Bax levels. Exposure of MCF7 and AGS cell lines to N. sativa caused a significant decrease in the expression of MMP2-9 and HSP60-70 genes over time, particularly at a dosage of 200 µg/mL compared to the control group (p < 0.05).Our findings indicate that N. sativa oil has a dose-dependent effect on cytotoxicity and the expression of apoptotic, heat shock proteins, and matrix metalloproteinases genes in breast and gastric cancer.
dc.description.urihttps://doi.org/10.1007/s11033-024-09453-1
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/38578469
dc.description.urihttps://hdl.handle.net/11552/8569
dc.description.urihttps://hdl.handle.net/20.500.12403/3148
dc.identifier.doi10.1007/s11033-024-09453-1
dc.identifier.eissn1573-4978
dc.identifier.issn0301-4851
dc.identifier.openairedoi_dedup___::ceab55a3c721573f42829a45196f854a
dc.identifier.orcid0000-0002-9826-2556
dc.identifier.orcid0000-0002-3617-899x
dc.identifier.orcid0000-0001-9260-5223
dc.identifier.pubmed38578469
dc.identifier.scopus2-s2.0-85189778144
dc.identifier.urihttps://hdl.handle.net/20.500.12597/41709
dc.identifier.volume51
dc.identifier.wos001197733900015
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.ispartofMolecular Biology Reports
dc.rightsCLOSED
dc.subjectAGS
dc.subjectHSPs
dc.subjectCaspase 3
dc.subjectMCF7
dc.subjectApoptosis
dc.subjectAntineoplastic Agents
dc.subjectN. sativa
dc.subjectStomach Neoplasms
dc.subjectCell Line, Tumor
dc.subjectMCF-7 Cells
dc.subjectHumans
dc.subjectMatrix Metalloproteinase 2
dc.subjectPlant Oils
dc.subjectMMPs
dc.subjectNigella sativa
dc.subjectRT PCR
dc.subjectHeat-Shock Proteins
dc.subjectbcl-2-Associated X Protein
dc.subjectCell Proliferation
dc.titleDetermination of anti-cancer effects of Nigella sativa seed oil on MCF7 breast and AGS gastric cancer cells
dc.typeArticle
dspace.entity.typePublication
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Additionally, the expression of the Caspase-3, BCL2/Bax, MMP2-9 and HSP60-70 gene was examined using RT-PCR in cell lines treating with N. sativa.The MTT experiments demonstrate that N. sativa has a time and dose-dependent inhibitory effect on the proliferation of MCF7 and AGS cancer cells. The vitality rates of MCF7 and AGS cells treated with N. sativa were 77.04-67.50% at 24 h, 65.28-39.14% at 48 h, and 48.95-32.31% at 72 h. The doses of 100 and 200 µg/mL were shown to be the most effective on both cancer cells. RT-PCR analysis revealed that N. sativa oil extract increased caspase-3 levels in both cell lines at higher concentrations and suppressed BCL2/Bax levels. 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