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dc.contributor.authorMohammadi, A
dc.contributor.authorMansoori, B
dc.contributor.authorAghapour, M
dc.contributor.authorShirjang, S
dc.contributor.authorNami, S
dc.contributor.authorBaradaran, B
dc.date.accessioned2018-08-26T05:36:30Z
dc.date.available2018-08-26T05:36:30Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39549
dc.description.abstractDue to the chemo resistant nature of cancer cells and adverse effects of current therapies, researchers are looking for the most efficient therapeutic approach which has the lowest side effects and the highest toxicity on cancer cells. The aim of the present study was to investigate the synergic effect of Urtica dioica extract in combination with paclitaxel on cell death and invasion of human breast cancer MDA-MB-468 cell line.To determine the cytotoxic effects of Urtica dioica extract with paclitaxel, MTT assay was performed. The scratch test was exploited to assess the effects of Urtica dioica, Paclitaxel alone and combination on migration of cancer cells. The expression levels of snail-1, ZEB1, ZEB2, twist, Cdc2, cyclin B1 and Wee1 genes were quantified using qRT-PCR and western blot performed for snail-1expression. The effects of plant extract, Paclitaxel alone and combination on different phases of cell cycle was analyzed using flow cytometry.Results of MTT assay showed that Urtica dioica significantly destroyed cancer cells. Interestingly, Concurrent use of Urtica dioica extract with paclitaxel resulted in decreased IC50 dose of paclitaxel. Moreover, findings of scratch assay exhibited the inhibitory effects of Urtica dioica, Paclitaxel alone and combination on migration of MDA-MB-468 cell line. Our findings also demonstrated that the extract substantially decreased the Snail-1 and related gene expression. Ultimately, Cell cycle arrest occurred at G2/M phase post-treatment by deregulating Cdc2 and wee1.Our results demonstrated that the dichloromethane extract of Urtica dioica inhibit cell growth and migration. Also, Urtica dioica extract substantially increased sensitivity of breast cancer cells to paclitaxel. Therefore, it can be used as a potential candidate for treatment of breast cancer with paclitaxel.
dc.language.isoEnglish
dc.relation.ispartofBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
dc.subjectBreast Neoplasms
dc.subjectCDC2 Protein Kinase
dc.subjectCell Cycle Checkpoints
dc.subjectCell Cycle Proteins
dc.subjectCell Death
dc.subjectCell Line, Tumor
dc.subjectCell Movement
dc.subjectCyclin-Dependent Kinases
dc.subjectDrug Synergism
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectInhibitory Concentration 50
dc.subjectNuclear Proteins
dc.subjectPaclitaxel
dc.subjectPlant Extracts
dc.subjectProtein-Tyrosine Kinases
dc.subjectRNA, Messenger
dc.subjectSnail Family Transcription Factors
dc.subjectUrtica dioica
dc.subjectWound Healing
dc.titleThe Urtica dioica extract enhances sensitivity of paclitaxel drug to MDA-MB-468 breast cancer cells.
dc.typearticle
dc.citation.volume83
dc.citation.spage835
dc.citation.epage842
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.biopha.2016.07.056


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