Morus Rubra Extract Induces Cell Cycle Arrest and Apoptosis in Human Colon Cancer Cells Through Endoplasmic Reticulum Stress and Telomerase

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Özet

Many studies have reported cytotoxic effects of different Morus species, but there have been only limited studies on the cytotoxic effect of Morus rubra. The aims of this study were to evaluate the cytotoxic effect of dimethyl sulfoxide extract of M. rubra and to investigate, for the first time, its probable cytotoxic activity in human colon cancer (WiDr) cells, together with the mechanism involved. The cytotoxic activity of extract was determined using MTT assay. The mechanism involved in the cytotoxic effect of extract was then evaluated in terms of apoptosis, and the cell cycle using flow cytometry, mitochondrial membrane potential (MMP) was investigated using the fluorometric method, and expression levels of telomerase and C/EBP homologous protein (CHOP) were investigated using reverse-transcription PCR (RT-PCR). M. rubra extract exhibited moderate selective cytotoxicity on colon cancer cells compared with fibroblast cells. Extract induced cell cycle arrest at the G1 phase and apoptosis via reduced MMP in WiDr cells. Additionally, M. rubra extract significantly repressed telomerase and induced CHOP expressions in WiDr cells. Our results demonstrate that targeting telomerase and endoplasmic reticulum stress represents a promising strategy in colon cancer therapy, and M. rubra may have considerable potential for development as a novel natural product-based anticancer agent.

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Tam Kayıt
AlanDeğerDil
dc.contributor.authorDemir, Selim
dc.contributor.authorTuran, Ibrahim
dc.contributor.authorAliyazicioglu, Yuksel
dc.contributor.authorKilinc, Kagan
dc.contributor.authorYaman, Serap Ozer
dc.contributor.authorAyazoglu Demir, Elif
dc.contributor.authorArslan, Ayse
dc.contributor.authorMentese, Ahmet
dc.contributor.authorDeger, Orhan
dc.date.accessioned2026-10-22T10:23:31.355452465Z
dc.date.available2026-10-22T10:23:31.355452465Z
dc.date.issued2017
dc.description.abstractMany studies have reported cytotoxic effects of different Morus species, but there have been only limited studies on the cytotoxic effect of Morus rubra. The aims of this study were to evaluate the cytotoxic effect of dimethyl sulfoxide extract of M. rubra and to investigate, for the first time, its probable cytotoxic activity in human colon cancer (WiDr) cells, together with the mechanism involved. The cytotoxic activity of extract was determined using MTT assay. The mechanism involved in the cytotoxic effect of extract was then evaluated in terms of apoptosis, and the cell cycle using flow cytometry, mitochondrial membrane potential (MMP) was investigated using the fluorometric method, and expression levels of telomerase and C/EBP homologous protein (CHOP) were investigated using reverse-transcription PCR (RT-PCR). M. rubra extract exhibited moderate selective cytotoxicity on colon cancer cells compared with fibroblast cells. Extract induced cell cycle arrest at the G1 phase and apoptosis via reduced MMP in WiDr cells. Additionally, M. rubra extract significantly repressed telomerase and induced CHOP expressions in WiDr cells. Our results demonstrate that targeting telomerase and endoplasmic reticulum stress represents a promising strategy in colon cancer therapy, and M. rubra may have considerable potential for development as a novel natural product-based anticancer agent.
dc.description.sponsorshipKaradeniz Technical University Scientific Research Foundation (Trabzon, Turkey)
dc.identifier.doi10.1080/01635581.2017.1247887
dc.identifier.eissn1532-7914
dc.identifier.endpage83
dc.identifier.issn0163-5581
dc.identifier.issue1
dc.identifier.pmid27880042
dc.identifier.scopus2-s2.0-84996619324
dc.identifier.startpage74
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/15052
dc.identifier.volume69
dc.identifier.wosWOS:000392619700008
dc.language.isoen
dc.publisherRoutledge
dc.relation.ispartofNutrition and Cancer
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject.classificationOncology
dc.subject.classificationNutrition & Dietetics
dc.subject.otherAntineoplastic Agents, Phytogenic
dc.subject.otherApoptosis
dc.subject.otherCell Cycle Checkpoints
dc.subject.otherCell Line, Tumor
dc.subject.otherCisplatin
dc.subject.otherColonic Neoplasms
dc.subject.otherEndoplasmic Reticulum Stress
dc.subject.otherGene Expression Regulation, Neoplastic
dc.subject.otherHumans
dc.subject.otherInhibitory Concentration 50
dc.subject.otherMembrane Potential, Mitochondrial
dc.subject.otherMorus
dc.subject.otherPlant Extracts
dc.subject.otherTelomerase
dc.subject.otherTranscription Factor CHOP
dc.subject.otherC EBP homologous protein
dc.subject.othercytotoxic agent
dc.subject.otherdimethyl sulfoxide
dc.subject.otherMorus rubra extract
dc.subject.othermulberry extract
dc.subject.otherprotein
dc.subject.otherunclassified drug
dc.subject.otherantineoplastic agent
dc.subject.otherDDIT3 protein, human
dc.subject.othergrowth arrest and DNA damage inducible protein 153
dc.subject.otherplant extract
dc.subject.otherantiproliferative activity
dc.subject.otherArticle
dc.subject.othercancer cell
dc.subject.othercell count
dc.subject.othercell cycle arrest
dc.subject.othercell cycle G1 phase
dc.subject.othercell cycle S phase
dc.subject.othercolon cancer
dc.subject.othercontrolled study
dc.subject.otherdrug mechanism
dc.subject.otherfibroblast
dc.subject.otherflow cytometry
dc.subject.otherfluorometry
dc.subject.othergene expression
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherIC50
dc.subject.othermitochondrial membrane potential
dc.subject.otherMorus rubra
dc.subject.otherMTT assay
dc.subject.othernonhuman
dc.subject.otherreverse transcription polymerase chain reaction
dc.subject.othercell cycle checkpoint
dc.subject.otherchemistry
dc.subject.othercolon tumor
dc.subject.otherdrug effects
dc.subject.othergene expression regulation
dc.subject.othergenetics
dc.subject.othermetabolism
dc.subject.otherpathology
dc.subject.othertumor cell line
dc.titleMorus Rubra Extract Induces Cell Cycle Arrest and Apoptosis in Human Colon Cancer Cells Through Endoplasmic Reticulum Stress and Telomerase
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex25
rdl.citation.scopus23
rdl.citation.wos24
rdl.departmentb Department of Genetic and Bioengineering , Faculty of Engineering and Natural Sciences, Gumushane University , Gumushane , Turkey
rdl.departmentc Medicinal Plants , Traditional Medicine Practice and Research Center, Gumushane University , Gumushane , Turkey
rdl.departmentf Department of Biotechnology , Institute of Science, Gumushane University , Gumushane , Turkey
rdl.oa.statusclosed
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)