Evidence map›Paper›PMID 42894051›Full record

ArticleBreast cancer research and treatment2026

Investigation of DNA methylation levels before and after treatment in breast cancer patients receiving neoadjuvant chemotherapy.

Halime Yildirim, Ender Coskunpinar, Mustafa Tukenmez, Baran Mollavelioglu, Aysel Bayram

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Article in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Halime YildirimDepartment of Medical Biology, Hamidiye School of Medicine, Saglik Bilimleri University, Selimiye Mah., Tibbiye Cad., No:38, Istanbul, 34668, Türkiye. hlmyildirim93@gmail.com.ORCID http://orcid.org/0000-0002-9008-7909
Ender CoskunpinarDepartment of Medical Biology, Hamidiye School of Medicine, Saglik Bilimleri University, Selimiye Mah., Tibbiye Cad., No:38, Istanbul, 34668, Türkiye.ORCID http://orcid.org/0000-0002-1003-5544
Mustafa TukenmezBreast Unit, Department of General Surgery, Istanbul Faculty of Medicine, Istanbul University, Istanbul, 34093, Türkiye.ORCID http://orcid.org/0000-0002-9403-568X
Baran MollaveliogluBreast Unit, Department of General Surgery, Istanbul Faculty of Medicine, Istanbul University, Istanbul, 34093, Türkiye.ORCID http://orcid.org/0000-0003-3152-044X
Aysel BayramDepartment of Pathology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, 34093, Türkiye.ORCID http://orcid.org/0000-0002-5014-0074

Funding

Saglik Bilimleri University Scientific Research Projects Unit 2024/098Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 125S228
6 · The paper itself

Abstract

purposeDrug resistance is a major cause of treatment failure in breast cancer patients. Numerous genetic and epigenetic markers have been proposed to influence Neoadjuvant Chemotherapy (NACT) response, and genes that regulate the effectiveness of chemotherapeutic agents undergo expression regulation via methylation. In this study, we aimed to investigate the methylation levels of KDM5A, KDM5B, and KDM5C, as well as their associated genes, EZH2, TFAP2C, ZMYND8, and SIN3B (Exon 1-2 and 19-20), in blood samples collected from patients before and after NACT treatment. Besides, we also examined potential variations in the KDM5A, KDM5B, and KDM5C gene regions.

methodsTwenty patients were diagnosed with breast cancer, and 30 healthy control individuals were included in the study. Blood samples were taken from the patients twice, before and after NACT. Methylation levels of KDM5 family genes and related genes were analyzed using Methylation-specific PCR (MSP). Additionally, potential variants in the KDM5A, KDM5B, and KDM5C gene regions were identified using Sanger sequencing.

resultsAccording to the methylation analysis results, the SIN3B (Exon 19-20), KDM5C, EZH2, and TFAP2C genes were prominent in patients with pathological partial response, while the KDM5A, KDM5B, KDM5C, EZH2, TFAP2C, and SIN3B (Exon 19-20) genes were prominent in patients with pathological complete response. According to genotyping results, rs41308616 and rs971896841 variants were detected as heterozygous in the KDM5C gene region in two patients, respectively.

conclusionThe methylation percentages and genetic variations in the KDM5 family and related gene regions identified in this study may serve as potential biomarkers for developing treatment strategies for breast cancer patients.

Indexed as

Breast NeoplasmsDNA MethylationAdultBiomarkers, TumorEpigenesis, GeneticFemaleGene Expression Regulation, NeoplasticHistone DemethylasesHumansJumonji Domain-Containing Histone DemethylasesMiddle AgedNeoadjuvant TherapyNuclear ProteinsRepressor ProteinsRetinoblastoma-Binding Protein 2Biomarkers, TumorHistone DemethylasesJumonji Domain-Containing Histone DemethylasesKDM5A protein, humanKDM5B protein, humanKDM5C protein, humanNuclear ProteinsRepressor ProteinsRetinoblastoma-Binding Protein 2Breast cancerChemotherapeutic resistanceEpigeneticsMethylationNeoadjuvant chemotherapy

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.