Evidence map›Paper›PMID 40574404›Full record

ArticleCurrent medicinal chemistry2026

Exploring the Role of DPF1 in Hepatocellular Carcinoma: Implications for Prognosis and Therapy.

Fan Yang, Yinyi Li, Dan Chen, Xiuju Wang, Mei Sun, Dongbing Li, Niansong Qian

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Article in Current medicinal chemistry, 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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5 · Who and what money

Authors and funding

7 authors.

Fan YangDepartment of Oncology, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100071, China.
Yinyi LiDepartment of Outpatient, the Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Dan ChenDepartment of Oncology, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100071, China.
Xiuju WangDepartment of Oncology, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100071, China.
Mei SunThe Fourth Reserve Asset Management Bureau, Qingdao, 266100, Shandong, China.
Dongbing LiScientific Research Center, Beijing ChosenMed Clinical Laboratory Co., Ltd. Beijing, 100176, China.ORCID 0000-0002-5227-9643
Niansong QianDepartment of Thoracic Oncology, Senior Department of Respiratory and Critical Care Medicine, the Eighth Medical Center of Chinese PLA General Hospital, Beijing 100091, China.ORCID 0000-0002-3297-4294

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a life-threatening cancer with rising incidence and mortality rates. Identifying new prognostic biomarkers is crucial for improving HCC management.

objectivesThis study investigates the role of Double PHD Fingers 1 (DPF1) in hepatocellular carcinoma (HCC), exploring its potential as a prognostic indicator and therapeutic target.

methodsWe analyzed DPF1 expression in 374 hepatocellular carcinoma (HCC) tissues and 50 normal tissues from the TCGA-HCC database, as well as in 240 HCC tissues and 202 normal tissues from the ICGC-HCC repository. We examined the correlation between DPF1 expression and clinical parameters, immune cell infiltration, drug response profiles, cancer stem cell (CSC) characteristics, and its diagnostic/prognostic potential using various bioinformatics tools and statistical analyses. Validation was performed using the ICGC and HPA databases, and qRT-PCR was used to confirm DPF1 expression in HCC cell lines.

resultsDPF1 exhibited abnormal expression in HCC and several other malignancies. Elevated DPF1 levels were significantly associated with higher Alpha-fetoprotein (AFP) levels (p = 0.043) and poorer clinical outcomes, including diminished overall survival (OS) (p = 0.002), progression-free survival (PFS) (p = 0.018), and disease-specific survival (DSS) (p = 0.001). DPF1 expression was also linked to immune cell infiltration, immune checkpoint gene expression, drug sensitivity, and CSC characteristics. Notably, DPF1 was significantly overexpressed in HCC tissues and cell lines at both transcriptional and translational levels.

conclusionOur study reveals that DPF1 is a novel prognostic biomarker in HCC, with potential implications for immunotherapy and drug resistance. Elevated DPF1 expression is associated with adverse clinical outcomes and may serve as a target for future therapeutic interventions in HCC.

Indexed as

Carcinoma, HepatocellularDNA-Binding ProteinsLiver NeoplasmsTranscription FactorsAntineoplastic AgentsBiomarkers, TumorCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplastic Stem CellsPrognosisAntineoplastic AgentsBiomarkers, TumorDNA-Binding ProteinsTranscription Factorscancer stem cellsDPF1drug sensitivityHepatocellular carcinomaimmune infiltrationprognosis

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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.