An Investigation of the Antiproliferative Effect of Rhododendron luteum Extract on Cervical Cancer (HeLa) Cells via Nrf2 Signaling Pathway

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Özet

The aim of the present study was to investigate the role of Rhododendron luteum extract (RLE) in the induction of Nrf2‑related oxidative stress and endoplasmic reticulum (ER) stress in human cervical cancer (HeLa) cells. The antiproliferative effect of RLE on HeLa and fibroblast cells was determined using the MTT assay. The effects of RLE on the cell cycle, apoptosis, and production of reactive oxygen species (ROS) in HeLa cells were evaluated using fluorescent probes. The mRNA expression levels of Nrf2 [and its targets glutamate-cysteine ligase catalytic subunit (GCLC), and glucose-6-phosphate dehydrogenase (G6PD)], and C/EBP homologous protein (CHOP, an ER stress marker were determined using reverse transcription‑quantitative polymerase chain reaction (RT-PCR). The results demonstrated that RLE exhibited a selective cytotoxic effect (2.9-fold) on HeLa cells compared to fibroblast cells. RLE arrested the cell cycle at the S phase, and induced apoptosis, ER stress, and ROS formation. In addition, RLE significantly suppressed the expression levels of Nrf2, GCLC and G6PD (0.65, 0.69, and 0.54-fold, respectively) and increased the expression of CHOP (4.48-fold) in HeLa cells at 72 h of treatment (p < 0.05). These results show that the antiproliferative effect of RLE occurs through the Nrf2 and ER stress pathways, and the results should now be supported by further in vivo studies.

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Tam Kayıt
AlanDeğerDil
dc.contributor.authorTuran, Ibrahim
dc.contributor.authorDemir, Selim
dc.contributor.authorYaman, Serap Ozer
dc.contributor.authorCanbolat, Deniz
dc.contributor.authorMentese, Ahmet
dc.contributor.authorAliyazicioglu, Yuksel
dc.date.accessioned2026-10-22T10:20:52.442275014Z
dc.date.available2026-10-22T10:20:52.442275014Z
dc.date.issued2022
dc.description.abstractThe aim of the present study was to investigate the role of Rhododendron luteum extract (RLE) in the induction of Nrf2‑related oxidative stress and endoplasmic reticulum (ER) stress in human cervical cancer (HeLa) cells. The antiproliferative effect of RLE on HeLa and fibroblast cells was determined using the MTT assay. The effects of RLE on the cell cycle, apoptosis, and production of reactive oxygen species (ROS) in HeLa cells were evaluated using fluorescent probes. The mRNA expression levels of Nrf2 [and its targets glutamate-cysteine ligase catalytic subunit (GCLC), and glucose-6-phosphate dehydrogenase (G6PD)], and C/EBP homologous protein (CHOP, an ER stress marker were determined using reverse transcription‑quantitative polymerase chain reaction (RT-PCR). The results demonstrated that RLE exhibited a selective cytotoxic effect (2.9-fold) on HeLa cells compared to fibroblast cells. RLE arrested the cell cycle at the S phase, and induced apoptosis, ER stress, and ROS formation. In addition, RLE significantly suppressed the expression levels of Nrf2, GCLC and G6PD (0.65, 0.69, and 0.54-fold, respectively) and increased the expression of CHOP (4.48-fold) in HeLa cells at 72 h of treatment (p < 0.05). These results show that the antiproliferative effect of RLE occurs through the Nrf2 and ER stress pathways, and the results should now be supported by further in vivo studies.
dc.description.sponsorshipGumushane University Scientific Research Foundation, (F5119.02.02)
dc.identifier.doi10.1080/01635581.2021.1955287
dc.identifier.eissn1532-7914
dc.identifier.endpage1893
dc.identifier.issn0163-5581
dc.identifier.issue5
dc.identifier.pmid34323135
dc.identifier.scopus2-s2.0-85111900692
dc.identifier.startpage1882
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/13048
dc.identifier.volume74
dc.identifier.wosWOS:000679276400001
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.otherApoptosis
dc.subject.otherFemale
dc.subject.otherHeLa Cells
dc.subject.otherHumans
dc.subject.otherNF-E2-Related Factor 2
dc.subject.otherPlant Extracts
dc.subject.otherReactive Oxygen Species
dc.subject.otherRhododendron
dc.subject.otherSignal Transduction
dc.subject.otherUterine Cervical Neoplasms
dc.subject.otherantimitotic agent
dc.subject.otherantioxidant
dc.subject.otherCCAAT enhancer binding protein
dc.subject.othercisplatin
dc.subject.othercytotoxic agent
dc.subject.othergallic acid
dc.subject.otherglucose 6 phosphate dehydrogenase
dc.subject.otherglutamate cysteine ligase
dc.subject.otherplant extract
dc.subject.otherquercetin
dc.subject.otherreactive oxygen metabolite
dc.subject.otherRhododendron luteum extract
dc.subject.otherunclassified drug
dc.subject.othertranscription factor Nrf2
dc.subject.otheramplicon
dc.subject.otherantioxidant activity
dc.subject.otherantiproliferative activity
dc.subject.otherArticle
dc.subject.othercontrolled study
dc.subject.otherdrug cytotoxicity
dc.subject.otherdrug determination
dc.subject.otherdrug screening
dc.subject.otherendoplasmic reticulum stress
dc.subject.otherfibroblast
dc.subject.otherHeLa cell line
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherIC50
dc.subject.othermRNA expression level
dc.subject.otherMTT assay
dc.subject.otherNrf2 signaling
dc.subject.otherreal time reverse transcription polymerase chain reaction
dc.subject.otherS phase cell cycle checkpoint
dc.subject.otherselectivity index
dc.subject.otheruterine cervix cancer
dc.subject.othergenetics
dc.subject.othermetabolism
dc.subject.otheruterine cervix tumor
dc.titleAn Investigation of the Antiproliferative Effect of Rhododendron luteum Extract on Cervical Cancer (HeLa) Cells via Nrf2 Signaling Pathway
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex13
rdl.citation.scopus15
rdl.citation.wos15
rdl.departmentDepartment of Genetic and Bioengineering, Faculty of Engineering and Natural Sciences, Gumushane University, Gumushane, Turkey
rdl.departmentDepartment 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)