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dc.contributor.authorMohammadi, A
dc.contributor.authorMansoori, B
dc.contributor.authorAghapour, M
dc.contributor.authorBaradaran, PC
dc.contributor.authorShajari, N
dc.contributor.authorDavudian, S
dc.contributor.authorSalehi, S
dc.contributor.authorBaradaran, B
dc.date.accessioned2018-08-26T09:40:35Z
dc.date.available2018-08-26T09:40:35Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58403
dc.description.abstractBackground: One of the major causes of cancer death internationally and the third most prevalent cancer in the world has been diagnosed with colorectal cancer. Although current routine treatments of cancer have been successful in some extent, mortality caused by adverse effects of these strategies is still raising. Medicinal plants are potential sources of anticancer compounds and can be exploited as a powerful complementary tool. This study aimed to investigate the cytotoxic effects of nettle extract on mouse colorectal cancer cells, HCT. Materials and Methods: In the present study, to evaluate the cytotoxicity of nettle extract, MTT assay and trypan blue were performed. Subsequently, DNA fragmentation and TUNEL test was carried out for determination of apoptosis. Real-time PCR test was used to quantify the expression of Caspase-3, Caspase-9, and Bcl-2 which is involved in apoptosis regulation. Finally, cell cycle analysis was conducted by using flow cytometry. Results: The results of MTT assay showed that the dichloromethane extract of U. dioica extract significantly destroyed cancer cells HCT-116. DNA fragmentation and TUNEL test demonstrated that Utrica extract elicited apoptotic response in the cancer cells. The messenger RNA (mRNA) expression levels of Caspase-3 and Caspase-9 markedly increased, while the Bcl-2 gene was conversely downregulated. Findings of flow cytometry confirmed that cell cycle arrest has occurred at the G2 phase. Conclusion: Taken together, our experiment showed that subjecting HCT-116 cells to dichloromethane extract of nettle (U. dioica), increases turnover of these cells. Thus, it may be a useful agent in the treatment of colorectal cancer. © 2016, Springer Science+Business Media New York.
dc.language.isoEnglish
dc.relation.ispartofJournal of Gastrointestinal Cancer
dc.subjectcaspase 3
dc.subjectcaspase 9
dc.subjectDNA
dc.subjectmessenger RNA
dc.subjectprotein bcl 2
dc.subjecttrypan blue
dc.subjectUrtica dioica extract
dc.subjectplant extract
dc.subjectadult
dc.subjectantineoplastic activity
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectDNA fragmentation
dc.subjectdown regulation
dc.subjectG2 phase cell cycle checkpoint
dc.subjectgene expression
dc.subjectHCT116 cell line
dc.subjectherbal medicine
dc.subjecthuman
dc.subjecthuman cell
dc.subjecthuman tissue
dc.subjectMTT assay
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectTUNEL assay
dc.subjectanimal
dc.subjectapoptosis
dc.subjectcell cycle checkpoint
dc.subjectcell proliferation
dc.subjectchemistry
dc.subjectColorectal Neoplasms
dc.subjectdrug effects
dc.subjectHCT 116 cell line
dc.subjectmiddle aged
dc.subjectmouse
dc.subjectpathology
dc.subjectUrtica dioica
dc.subjectAdult
dc.subjectAnimals
dc.subjectApoptosis
dc.subjectCell Cycle Checkpoints
dc.subjectCell Proliferation
dc.subjectColorectal Neoplasms
dc.subjectHCT116 Cells
dc.subjectHumans
dc.subjectMice
dc.subjectMiddle Aged
dc.subjectPlant Extracts
dc.subjectUrtica dioica
dc.titleThe Herbal Medicine Utrica Dioica Inhibits Proliferation of Colorectal Cancer Cell Line by Inducing Apoptosis and Arrest at the G2/M Phase
dc.typeArticle
dc.citation.volume47
dc.citation.issue2
dc.citation.spage187
dc.citation.epage195
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1007/s12029-016-9819-3


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