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

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

PMC · DOI: 10.3390/v17050653 · Viruses · 2025-04-30

## TL;DR

This study classifies the LC4 cell line as a model for HIV-HCV-induced HCC, showing immune evasion and metabolic changes relevant for drug testing.

## Contribution

The paper introduces LC4 as a novel primary-like HCC cell line derived from an HIV-HCV co-infected patient for preclinical research.

## Key findings

- LC4 cells show immunosuppression and metabolic reprogramming similar to the parental tumor tissue.
- Drug-metabolizing enzymes are downregulated in LC4 cells, suggesting alternate metabolic pathways.
- LC4 cells share specific biomarkers with global HCC datasets and parental tissue.

## Abstract

Background: Hepatocellular 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. Methods: We 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. Results: LC4 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. Conclusions: We 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.

## Linked entities

- **Diseases:** Hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** CDK4 (cyclin dependent kinase 4) [NCBI Gene 1019] {aka CMM3, MCPH31, PSK-J3}
- **Diseases:** HIV (MESH:D015658), cancer (MESH:D009369), HCC (MESH:D006528)
- **Cell lines:** LC4 — Homo sapiens (Human), Childhood B acute lymphoblastic leukemia, Cancer cell line (CVCL_1374)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12115383/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12115383/full.md

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Source: https://tomesphere.com/paper/PMC12115383