Isthmin-1 and spexin as promising novel biomarker candidates for invasive ductal breast carcinoma

dc.contributor.authorTurk, Ahmet
dc.contributor.authorMetin, Tuba Ozcan
dc.contributor.authorKuloglu, Tuncay
dc.contributor.authorYilmaz, Mustafa
dc.contributor.authorArtas, Gokhan
dc.contributor.authorOzercan, I. Hanifi
dc.contributor.authorHancer, Serhat
dc.date.accessioned2026-08-12T18:11:02Z
dc.date.issued2024
dc.departmentFırat Üniversitesi
dc.description.abstractIntroduction: Breast cancer is one of the most common malignant tumors and a leading cause of cancer-related death in women. Research is focusing on biomarkers linked to breast cancer, particularly two novel proteins: isthmin-1 (ISM-1) and spexin (SPX), which require further investigation. Material and methods: The study involved 20 healthy controls and 60 patients with invasive ductal carcinoma, categorized into three groups: Grade I (n=20), Grade II (n=20), and Grade III (n=20). Levels of ISM-1 and SPX in tissue were analyzed using immunohistochemistry alongside the clinicopathologic data of patients. Results: There were no statistically significant differences in age, menopausal status, ER, PR, and Cerb-B2 values across grades (p>0.05). Tumor diameters showed a significant increase in Grade I compared to Grade II (p<0.05), while no significant difference was noted between Grade II and Grade III, although diameters were larger in Grade III compared to Grade I (p<0.05). Notably, ISM-1 immunoreactivity decreased, and SPX immunoreactivity increased significantly across all grades compared to normal tissue (p<0.05), with no significant differences between tumor grades for these markers (p>0.05). Conclusions: This study presents new findings on ISM-1 and SPX expression in invasive ductal breast carcinoma. The decrease in ISM-1 and increase in SPX suggest a need for further research into the relationship between adipokines and tumor development in breast cancer.
dc.identifier.doi10.1016/j.tice.2024.102601
dc.identifier.issn0040-8166
dc.identifier.orcid0000-0002-4457-428X
dc.identifier.orcid0000-0003-0903-3522
dc.identifier.pmid39520846
dc.identifier.scopus2-s2.0-85208234087
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://doi.org/10.1016/j.tice.2024.102601
dc.identifier.urihttps://hdl.handle.net/11508/63526
dc.identifier.volume91
dc.identifier.wosWOS:001355973500001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherChurchill Livingstone
dc.relation.ispartofTissue & Cell
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectBreast cancer
dc.subjectInvasive ductal carcinoma
dc.subjectIsthmin-1
dc.subjectSpexin
dc.titleIsthmin-1 and spexin as promising novel biomarker candidates for invasive ductal breast carcinoma
dc.typeArticle

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