Evidence map›Paper›PMID 41373809›Full record

ArticleInternational journal of molecular sciences2025

ALKBH7 and NLRP3 Co-Expression: A Potential Prognostic and Immunometabolic Marker Set in Breast Cancer Subtypes.

Adem Senturk, Nur Kazan, Selen Sen, Gozde Cakirsoy Cakar, Lacin Tatliadim Sert, Fuldem Mutlu, Onur Taydas, Barıs Mantoglu, Yasemin Gunduz, Metin Ercan and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Adem SenturkDepartment of Surgical Oncology, Sakarya University, Sakarya Training and Research Hospital, 54100 Sakarya, Turkey.ORCID 0000-0002-7626-4649
Nur KazanDepartment Field Crops Division, Graduate Education Institute, Sakarya University of Applied Sciences, 54100 Sakarya, Turkey.ORCID 0000-0002-9032-9146
Selen SenDepartment of Pharmacy Services, Pamukova Vocational School, Sakarya University of Applied Sciences, 54100 Sakarya, Turkey.ORCID 0000-0002-5138-9488
Gozde Cakirsoy CakarDepartment of Medical Pathology, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.
Lacin Tatliadim SertDepartment of Internal Medical Sciences, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.
Fuldem MutluDepartment of Internal Medical Sciences, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.
Onur TaydasDepartment of Internal Medical Sciences, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.ORCID 0000-0002-9881-7240
Barıs MantogluDepartment of General Surgery, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.
Yasemin GunduzDepartment of Internal Medical Sciences, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.
Metin ErcanDepartment of Surgical Oncology, Sakarya University, Sakarya Training and Research Hospital, 54100 Sakarya, Turkey.
Zulfu BayhanDepartment of General Surgery, Faculty of Medicine, Sakarya University, 54100 Sakarya, Turkey.
Emine YildirimDepartment of General Surgery, Faculty of Medicine, Istanbul Atlas University, 34403 Istanbul, Turkey.
Hafize UzunDepartment of Medical Biochemistry, Faculty of Medicine, Istanbul Atlas University, 34403 Istanbul, Turkey.ORCID 0000-0002-1347-8498

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer (BC) is a heterogeneous disease with distinct molecular subtypes that exhibit variable immune responses and metabolic profiles. Recent studies have suggested that immunometabolic pathways play a role in tumor progression and treatment resistance. This study investigates the expression patterns of ALKBH7 and NLRP3 across BC molecular subtypes and explores their relationships with clinicopathological parameters and potential immunometabolic profiles. A total of 118 BC patients were classified into HER2+, TNBC, Luminal A, and Luminal B subtypes. Gene expression levels of ALKBH7 and NLRP3 were analyzed using quantitative real-time PCR (qRT-PCR), and correlations with clinical markers were assessed. ALKBH7 and NLRP3 expression levels varied significantly between subtypes, with the highest expression observed in HER2+ tumors. Strong positive correlations were found between ALKBH7 and NLRP3 in all subtypes, particularly in HER2+ (r = 0.812,

Indexed as

Biomarkers, TumorBreast NeoplasmsNLR Family, Pyrin Domain-Containing 3 ProteinAdultAgedFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedPrognosisBiomarkers, TumorNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanALKBH7breast cancerHER2+Ki-67Luminal ALuminal Btriple-negative breast cancer

Identifiers

PMID41373809
PMCPMC12691784

What Socratic holds

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Registered trials

None linked

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 Socratic graph.