نمایش مختصر رکورد

dc.contributor.authorSargazi, Samanen_US
dc.contributor.authorMoudi, Mahdiyehen_US
dc.contributor.authorKooshkaki, Omiden_US
dc.contributor.authorMirinejad, Shekoufehen_US
dc.contributor.authorSaravani, Raminen_US
dc.date.accessioned1399-07-30T21:01:27Zfa_IR
dc.date.accessioned2020-10-21T21:01:27Z
dc.date.available1399-07-30T21:01:27Zfa_IR
dc.date.available2020-10-21T21:01:27Z
dc.date.issued2020-09-01en_US
dc.date.issued1399-06-11fa_IR
dc.date.submitted2018-10-13en_US
dc.date.submitted1397-07-21fa_IR
dc.identifier.citationSargazi, Saman, Moudi, Mahdiyeh, Kooshkaki, Omid, Mirinejad, Shekoufeh, Saravani, Ramin. (2020). Hydro-alcoholic Extract of Achillea Wilhelmsii C. Koch Reduces the Expression of Cell Death-Associated Genes while Inducing DNA Damage in HeLa Cervical Cancer Cells. Iranian Journal of Medical Sciences, 45(5), 359-367. doi: 10.30476/ijms.2020.72657.0en_US
dc.identifier.issn0253-0716
dc.identifier.issn1735-3688
dc.identifier.urihttps://dx.doi.org/10.30476/ijms.2020.72657.0
dc.identifier.urihttps://ijms.sums.ac.ir/article_46737.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/439974
dc.description.abstractBackground: Achillea wilhelmsii C. Koch hydroalcoholic extract (AWHE) is proven to induce cell death. Previous studies suggested that AWHE is an effective inhibitor against the proliferation of prostate cancer cells. The present study aimed to evaluate possible alterations of cell death-associated genes and determine the growth inhibitory activity of AWHE on HeLa cervical cancer cells. <br />Methods: The antiproliferative activity of AWHE was tested using the tetrazolium dye-based colorimetric assay (MTT assay). The mRNA levels of Vascular endothelial growth factor (VEGF), caspase-3, and Breast Cancer Susceptibility gene 1 (BRCA1) were measured using the real-time Polymerase Chain Reaction method. The in-cell levels of phosphorylated H2AX were determined using the in-cell ELISA method. The data were analyzed using the non-parametric ANOVA and Friedman tests. p Results: Based on the MTT assay, The half-maximal inhibitory concentration and 81.99 µg/mL, respectively. The mRNA levels of BRCA1 increased after 12 and 24 hours of treatment (p <0.001), while the mRNA levels of VEGF significantly decreased after 12 hours (P=0.003) and 24 hours (P=0.001). Caspase-3 expression was increased in the HeLa cells after 6 and 12 hours (p <0.001) whereas γ-H2AX levels significantly increased after 24 and 48 hours of treatment (p <0.001). <br />Conclusion: AWHE possesses growth inhibitory activity by altering the expression of cell death-associated genes. Using extracts from herbal plants may provide alternative strategies to be deployed in the fight against cancer.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherShiraz University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.30476/ijms.2020.72657.0
dc.subjectAchilleaen_US
dc.subjectUterine cervical neoplasmsen_US
dc.subjectCell deathen_US
dc.subjectDNA Repairen_US
dc.titleHydro-alcoholic Extract of Achillea Wilhelmsii C. Koch Reduces the Expression of Cell Death-Associated Genes while Inducing DNA Damage in HeLa Cervical Cancer Cellsen_US
dc.typeTexten_US
dc.typeOriginal Article(s)en_US
dc.contributor.departmentCellular and Molecular Research Center, Resistant Tuberculosis Institute, Zahedan University of Medical Sciences, Zahedan, Iranen_US
dc.contributor.departmentDepartment of Medical Genetics, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iranen_US
dc.contributor.departmentDepartment of Immunology, School of Medicine, Birjand University of Medical Sciences, Birjand, Iranen_US
dc.contributor.departmentCellular and Molecular Research Center, Resistant Tuberculosis Institute, Zahedan University of Medical Sciences, Zahedan, Iranen_US
dc.contributor.departmentCellular and Molecular Research Center, Resistant Tuberculosis Institute, Zahedan University of Medical Sciences, Zahedan, Iranen_US
dc.citation.volume45
dc.citation.issue5
dc.citation.spage359
dc.citation.epage367
nlai.contributor.orcid0000-0002-2255-5977
nlai.contributor.orcid0000-0003-1941-3617


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