Evidence map›Paper›PMID 41102682›Full record

ArticleBMC cancer2025

Analysis of FNDC1 as a diagnostic marker and potential therapeutic target for ovarian serous cancer.

Hongying Jiao, Jing Tian, Qiao Liu, Meng Jiang, Xia Niu, Wei Zhang, Li Gong

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Article in BMC cancer, 2025. 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

7 authors.

Hongying Jiao *Department of Pathology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, 710038, China.
Jing Tian *Department of Pathology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, 710038, China.
Qiao LiuDepartment of Pathology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, 710038, China.
Meng JiangA Precision Medicine Research Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, China.
Xia NiuDepartment of Pathology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, 710038, China.
Wei ZhangDepartment of Pathology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, 710038, China. zhwlyh@fmmu.edu.cn.
Li GongDepartment of Pathology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, 710038, China. lotus1909@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFibronectin type III domain containing 1 (FNDC1) is a member of fibronectin type III domain protein family, which is known to play an important role in the metastasis of some cancers. However, it has not been reported about the relationship between FNDC1 and ovarian serous cancer.

methodsFirstly, we investigated the expression of FNDC1 in various cancer types, and analyzed its diagnostic value and potential role in ovarian serous cancer using TCGA database. Subsequently, a series of bioinformatics methods were used to explore the potential oncogenic effects of FNDC1, including the relationship between FNDC1 expression and immune cell infiltration and immune checkpoint molecules, protein-protein interaction network, gene ontology and Kyoto Encyclopedia of Genes and Genomes analysis, gene set enrichment analysis, and toxicity analysis. Finally, the results were further verified by cell function experiments.

resultsFNDC1 was highly expressed in ovarian serous cancer, which was further verified in cell line, indicating that it might be as a diagnostic marker of ovarian serous cancer. In addition, the expression of FNDC1 and TNFSF4, an immune checkpoint molecule, showed a strong positive correlation, and both them were involved in the same signaling pathway, indicating that they might jointly affect T-cell responses in ovarian serous cancer. Moreover, this effect might be inhibited by austocystin D.

conclusionFNDC1 was a potential diagnostic marker, prognostic indicator, and target for the treatment of ovarian serous cancer.

Indexed as

Biomarkers, TumorCystadenocarcinoma, SerousFibronectinsOvarian NeoplasmsCell Line, TumorComputational BiologyFemaleGene Expression Regulation, NeoplasticHumansPrognosisProtein Interaction MapsBiomarkers, TumorFibronectinsDiagnostic markerFNDC1Ovarian serous cancerTherapeutic target

Identifiers

PMID41102682
PMCPMC12532397

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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.