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Quercetin-Mediated Modulation of Tumor Suppressor miR-15a, miR-34a, and p53 Signaling in MCF-7 Breast Cancer Cells

dc.contributor.authorÇiğdem Güngörmez
dc.contributor.authorHatice Gumushan Aktas
dc.contributor.authorZeynep Çelik
dc.contributor.authorBüşra Ergin
dc.date.accessioned2025-07-21T07:16:40Z
dc.date.available2025-07-21T07:16:40Z
dc.date.issued2025-05-26
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü
dc.description.abstractBreast cancer remains one of the most prevalent types of cancer among women globally, contributing significantly to cancer-related mortality. Despite advancements in treatment, many cases continue to exhibit resistance to chemotherapy, radiotherapy, and hormonal therapies, often resulting in drug resistance, high recurrence rates, and severe side effects. Consequently, the role of the natural food components in cancer prevention and treatment is gaining increasing attention in modern medicine. This study focuses on quercetin, a phytochemical compound, and its effects on the breast cancer cell line MCF-7. Specifically, the study has investigated changes in the expression of miR-15a and miR-34a—microRNAs (miRNAs) known to regulate gene expression at the post-transcriptional level—and the P53 gene, which is critically involved in apoptosis. The analysis was performed using quantitative polymerase chain reaction (qPCR) and Western blot techniques. The results demonstrated that quercetin treatment at concentrations of 40 µM and 80 µM led to a 1.34-fold and 2.73-fold increase in P53 gene expression, respectively. Additionally, the tumor suppressor miRNA miR-15a showed expression changes of 1.48-fold and 1.69-fold at the same quercetin concentrations. Similarly, miR-34a expression levels increased by 1.23-fold and 1.39-fold at 40 µM and 80 µM, respectively. These findings suggest that dietary phytochemicals, such as quercetin, may have therapeutic potential by modulating miRNA expression and targeting the p53 pathway. In conclusion, quercetin emerges as a promising natural therapeutic agent for breast cancer, warranting further in vivo studies and clinical trials to confirm its efficacy and explore its potential as a part of combination therapies.
dc.identifier.citationGüngörmez, Ç., Aktas, H. G., Çelik, Z., & Ergin, B. Quercetin-Mediated Modulation of Tumor Suppressor miR-15a, miR-34a, and p53 Signaling in MCF-7 Breast Cancer Cells. Commagene Journal of Biology, 9(1), 80-85.
dc.identifier.doi10.31594/commagene.1662649
dc.identifier.issn2602-456X
dc.identifier.issue1
dc.identifier.scopus2-s2.0-105010266170
dc.identifier.scopusqualityN/A
dc.identifier.trdizinid1323749
dc.identifier.urihttps://doi.org/10.31594/commagene.1662649
dc.identifier.urihttps://hdl.handle.net/20.500.12604/8791
dc.identifier.volume9
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.institutionauthorGüngörmez, Çiğdem
dc.language.isoen
dc.publisherCommagene Journal of Biology
dc.relation.ispartofCommagene Journal of Biology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcancer
dc.subjectFlavonoids
dc.subjectnon-coding RNAs
dc.subjectP53
dc.titleQuercetin-Mediated Modulation of Tumor Suppressor miR-15a, miR-34a, and p53 Signaling in MCF-7 Breast Cancer Cells
dc.typeArticle
oaire.citation.issue1
oaire.citation.volume9

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