Rubus sanctus Schreb. root extract alters the MicroRNA expression and inhibits tumor activities of colorectal cancer cell lines

dc.contributor.buuauthorAlemdar, Adem
dc.contributor.buuauthorTunca, Berrin
dc.contributor.buuauthorMalyer, Hulisi
dc.contributor.buuauthorŞahin, Saliha
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.contributor.orcid0000-0002-1619-6680tr_TR
dc.contributor.researcheridABI-6078-2020tr_TR
dc.contributor.researcheridAAH-2892-2021tr_TR
dc.contributor.researcheridHIZ-7332-2022tr_TR
dc.contributor.scopusid57190943001tr_TR
dc.contributor.scopusid6602965754tr_TR
dc.contributor.scopusid6602736554tr_TR
dc.contributor.scopusid15027401600tr_TR
dc.date.accessioned2024-01-23T07:18:53Z
dc.date.available2024-01-23T07:18:53Z
dc.date.issued2018
dc.description.abstractBackground: Colorectal cancer (CRC) is one of the most common cancers in the world. Although surgical and screening techniques have vastly improved in the last 30 years, chemotherapeutics have not advanced sufficiently for successful treatment. Objective: The aim of this study is to investigate the microRNA (miRNA) expression changes and anticancer agent potential of Rubus Sanctus Schreb. root extract (RRE) on LoVo and HT-29 colorectal adenocarcinoma cell lines. Materials and Methods: LoVo and HT-29 CRC cell lines treated with different concentrations of RRE to find growth inhibitory effect with WST-1 assay. Fifty percent growth inhibition and 25% growth inhibition concentrations further evaluated with annedn V, total caspase, cell cycle, and migration assays. Real-time polymerase chain reaction was used to investigate the expression differences in miRNA after extract treatment. Results: Cell proliferation was reduced 77.98% in HT-29 cells after RRE treatment (P< 0.05). In the cell invasion analysis, RRE reduced invasion in both cell lines up to 75.56% (P< 0.05). In addition, RRE induced apoptosis in up to 98% of a cell population (P < 0.05). Similarly, pan-caspase activity increased to 976% and 87.2% in LoVo and HT-29 cell lines, respectively (P < 0.0001). After extract treatment, among the nine miRNAs evaluated, only miR-140 expression was significantly increased in both cell lines after RRE treatment (P< 0.05). Conclusion: Our data show for the first time that RRE has the capability to inhibit CRC cell proliferation and invasion and alter epigenetic mechanisms. Although further studies should be conducted on this topic, RRE is thought to be a potential candidate for the future studies regarding new therapy options.en_US
dc.identifier.citationAlemdar, A. vd. (2018). ''Rubus sanctus Schreb. root extract alters the MicroRNA expression and inhibits tumor activities of colorectal cancer cell lines''. Pharmacognosy Magazine, 14(55), Supplement S, S92-S101.en_US
dc.identifier.doihttps://doi.org/10.4103/pm.pm_357_17en_US
dc.identifier.eissn0976-4062
dc.identifier.endpageS101tr_TR
dc.identifier.issn0973-1296
dc.identifier.issue55 Supplement Sen_US
dc.identifier.scopus2-s2.0-85052653847tr_TR
dc.identifier.startpageS92tr_TR
dc.identifier.urihttps://phcog.com/article/view/2018/14/55s/s92-s101en_US
dc.identifier.urihttps://hdl.handle.net/11452/39255en_US
dc.identifier.volume14tr_TR
dc.identifier.wos000442782500017tr_TR
dc.indexed.pubmedPubMeden_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherSage Puplications Indiaen_US
dc.relation.bapKUAP (T)-2013/72tr_TR
dc.relation.journalPharmacognosy Magazineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPharmacology & pharmacyen_US
dc.subjectApoptosisen_US
dc.subjectBlackberryen_US
dc.subjectColorectal canceren_US
dc.subjectInvasionen_US
dc.subjectMicroRNARuen_US
dc.subjectBus sanctus Schreb.en_US
dc.subjectMedicinal-plantsen_US
dc.subjectBlack-raspberryen_US
dc.subjectApoptosisen_US
dc.subjectProliferationen_US
dc.subjectAnthocyaninsen_US
dc.subjectSuppressionen_US
dc.subjectSurvivalen_US
dc.subjectProteinen_US
dc.subjectGrowthen_US
dc.subjectGenesen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeB Raf kinaseen_US
dc.subject.emtreeCaspaseen_US
dc.subject.emtreeEllagic aciden_US
dc.subject.emtreeEpidermal growth factor receptoren_US
dc.subject.emtreeEpidermal growth factor receptor 2en_US
dc.subject.emtreeK ras proteinen_US
dc.subject.emtreeMicroRNAen_US
dc.subject.emtreeMiR 140en_US
dc.subject.emtreePlant extracten_US
dc.subject.emtreeProtein bcl 2en_US
dc.subject.emtreeProtein p53en_US
dc.subject.emtreeRubus sanctus extracten_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeAntiproliferative activityen_US
dc.subject.emtreeApoptosisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCancer inhibitionen_US
dc.subject.emtreeCell cycle arresten_US
dc.subject.emtreeCell invasionen_US
dc.subject.emtreeColorectal cancer cell lineen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDNA fragmentationen_US
dc.subject.emtreeHT-29 cell lineen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeLoVo cell lineen_US
dc.subject.emtreeMigration inhibitionen_US
dc.subject.emtreePlant rooten_US
dc.subject.emtreeRubusen_US
dc.subject.emtreeRubus sanctusen_US
dc.subject.scopusFragaria; Ribes; Antioxidanten_US
dc.subject.wosChemistry, medicinalen_US
dc.titleRubus sanctus Schreb. root extract alters the MicroRNA expression and inhibits tumor activities of colorectal cancer cell linesen_US
dc.typeArticleen_US
dc.wos.quartileQ4 (Chemistry, Medicinal)en_US

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