Publication:
Value of miR-31 and miR-150-3p as diagnostic and prognostic biomarkers for breast cancer

dc.contributor.authorErtürk, Elif
dc.contributor.authorArı, Ferda
dc.contributor.authorOnur, Ömer Enes
dc.contributor.authorMustafa, Şehsuvar
dc.contributor.authorTolunay, Şahsine
dc.contributor.buuauthorERTÜRK, ELİF
dc.contributor.buuauthorARI, FERDA
dc.contributor.buuauthorOnur, Ömer Enes
dc.contributor.buuauthorGÖKGÖZ, MUSTAFA ŞEHSUVAR
dc.contributor.buuauthorTOLUNAY, ŞAHSİNE
dc.contributor.departmentSağlık Hizmetleri Meslek Yüksekokulu
dc.contributor.departmentFen-Edebiyat Fakültesi
dc.contributor.departmentBiyoloji Bölümü
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGenel Cerrahi Ana Bilim Dalı
dc.contributor.departmentPatoloji Ana Bilim Dalı
dc.contributor.orcid0000-0002-6729-7908
dc.contributor.researcheridHOF-9934-2023
dc.contributor.researcheridAAG-7012-2021
dc.contributor.researcheridAAI-1612-2021
dc.contributor.researcheridJYH-6112-2024
dc.contributor.researcheridLLY-9034-2024
dc.date.accessioned2025-01-22T10:20:19Z
dc.date.available2025-01-22T10:20:19Z
dc.date.issued2024-12-01
dc.description.abstractBackground The most prevalent malignancy among women is breast cancer (BC). MicroRNAs (miRNAs) play a role in the initiation and progression of BC by influencing breast cancer stem cells (BCSCs) but the diagnostic and prognostic roles of those miRNAs on BC patients are still unknown. It was aimed to investigate expression profiles, diagnostic and prognostic potentials of BCSC-related miRNAs in different subtypes (Luminal A and B, HER2 + and TNBC) of BC patients. Methods and Results Expression analysis of 15 BCSC-related miRNAs was performed in 50 breast tumor tissues and 20 adjacent non-tumor tissues obtained from BC patients using the qRT-PCR method. The expression levels of miR-31 and miR-150-3p were significantly upregulated in the tumor tissues compared to the adjacent non-tumor tissues (p < 0.05). miR-31 expression upregulated in the Luminal A and Luminal B group compared to non-tumor tissue (p < 0.05). miR-31 expression was determined to be significantly higher in the Luminal group (Luminal A and B) compared to the aggressive group (HER2 + and TNBC) (p < 0.05). According to the ROC analysis, the area under the curve (AUC) of miR-31 and miR-150-3p were 0.66 with a sensitivity of 68% and a specificity of 70%. A significant inverse correlation was observed between miR-31 expression with metastatic carcinoma status, in situ component, and Ki67 value in tumors, and high miR-150-3p expression was correlated with p63 expression (p < 0.05). Conclusion miR-31 and miR-150-3p have the potential to serve as biomarkers for guiding diagnosis, evaluating prognosis, and metastatic process in patients with BC.
dc.identifier.doi10.1007/s11033-024-09958-9
dc.identifier.issn0301-4851
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85205447179
dc.identifier.urihttps://doi.org/10.1007/s11033-024-09958-9
dc.identifier.urihttps://link.springer.com/article/10.1007/s11033-024-09958-9
dc.identifier.urihttps://hdl.handle.net/11452/49676
dc.identifier.volume51
dc.identifier.wos001326707500002
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherSpringer
dc.relation.bapDDP(F)-2020/5
dc.relation.journalMolecular Biology Reports
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectStem-cells
dc.subjectMirnas
dc.subjectBreast cancer
dc.subjectMirna
dc.subjectCancer stem cell
dc.subjectBiomarker
dc.subjectBiochemistry & molecular biology
dc.titleValue of miR-31 and miR-150-3p as diagnostic and prognostic biomarkers for breast cancer
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentSağlık Hizmetleri Meslek Yüksekokulu
local.contributor.departmentFen-Edebiyat Fakültesi/Biyoloji Bölümü
local.contributor.departmentTıp Fakültesi/Genel Cerrahi Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Patoloji Ana Bilim Dalı
local.indexed.atWOS
local.indexed.atScopus
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relation.isAuthorOfPublication7b478372-ad3a-4f0a-a336-3ebde58856eb
relation.isAuthorOfPublication13dc6562-e9fe-42fa-8973-dcd80444844e
relation.isAuthorOfPublication.latestForDiscovery54fbb8ee-6806-4d77-9430-9b360d81a2ab

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