Evidence map›Paper›PMID 40431665›Full record

ArticleViruses2025

Classification of the LC4 Primarily-like Cell Line-Recapitulating a CDK4 Overexpressing Immune Evasive HIV-HCV-Induced HCC.

Janine Kah, Lisa Staffeldt, Tassilo Volz, Kornelius Schulze, Asmus Heumann, Götz Rövenstrunk, Meike Goebel, Sven Peine, Maura Dandri, Stefan Lüth

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Article in Viruses, 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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2 · The registry

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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

10 authors.

Janine KahDepartment of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Lisa StaffeldtDepartment of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0009-0002-1205-0155
Tassilo VolzDepartment of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0003-3120-8958
Kornelius SchulzeDepartment of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Asmus HeumannDepartment of General, Visceral and Thoracic Surgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Götz RövenstrunkFaculty of Health Sciences Brandenburg, Brandenburg Medical School Theodor Fontane, 16816 Neuruppin, Germany.
Meike GoebelInstitute for Transfusion Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Sven PeineInstitute for Transfusion Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Maura DandriDepartment of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0002-0073-6689
Stefan LüthFaculty of Health Sciences Brandenburg, Brandenburg Medical School Theodor Fontane, 16816 Neuruppin, Germany.

Funding

Deutsche Forschungsgemeinschaft KA 5390/2-1Ministry of Science Research and Cultural Affairs of the State of Brandenburg
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality. HCC is characterized by high heterogeneity and, subsequently, adaptation by developing resistance to current treatments. Applying individualized models is crucial to understanding the potential of approved therapies. Therefore, we classify a primary-like cell line derived from the core region of an HCC with underlying HIV-HCV co-infection employing deep analysis on the pathway regulation level.

methodsWe employed DEG analysis, followed by pathway analysis, to characterize the preservation level of the LC4 cells and the level of adoption. Next, we classify the new model for HCC research by employing healthy donor samples, commonly used HCC cell lines, and global RNAseq datasets.

resultsLC4 cells reflect the characteristics of the parental cancer region, including immunosuppression and metabolic reprogramming, characterized by the downregulation of drug-metabolizing enzymes compared to healthy individuals, indicating a transition to alternate metabolic pathways. Moreover, we identified specific biomarkers equally regulated in the parental tissue, in global datasets of the same entities as well as in LC4 cells.

conclusionsWe classified LC4 cells as an individual immunosuppressive and highly progressive primary-like HCC cell line. LC4 cells are applicable as a model for preclinical drug testing, minimizing the lack of preclinical models in HCV-HIV-induced HCC research.

Indexed as

Carcinoma, HepatocellularCyclin-Dependent Kinase 4Hepatitis CHIV InfectionsLiver NeoplasmsCell Line, TumorCoinfectionHepacivirusHumansCDK4 protein, humanCyclin-Dependent Kinase 4drug resistancemetabolic reprogrammingpersonalized therapyviral-induced hepatocellular carcinoma

Identifiers

PMID40431665
PMCPMC12115383

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