# Concordance of cancer-associated cytokines and mitochondrial DNA deletions in individuals with hepatocellular carcinoma and people living with HIV in Ghana

**Authors:** James Odame Aboagye, Ruth Ayanful-Torgby, Lei Zhou, Prince Peter Wormenor, Vincent Ganu, Kenneth Tachi, Bernard Nii Akrashie Attoh, Miriam Mensah, Timothy Kuuguu, Sedzro Kojo Mensah, George Boateng Kyei, Elijah Paintsil

PMC · DOI: 10.1186/s12876-025-04399-5 · BMC Gastroenterology · 2025-11-11

## TL;DR

This study found similar cytokine levels and mitochondrial DNA deletions in people with liver cancer and those living with HIV in Ghana, suggesting a link between HIV and cancer risk.

## Contribution

The study is the first to compare cytokine profiles and mtDNA deletions in HCC patients and PLWH in Ghana.

## Key findings

- Cytokines TGF-β, FGF2, IL-8, TNF-α, VEGFA, and RANTES were similarly elevated in HCC patients and PLWH.
- mtDNA deletions were comparably high in both HCC and HIV groups.
- The findings suggest a shared inflammatory and mitochondrial dysfunction profile between HCC and HIV.

## Abstract

Hepatocellular carcinoma (HCC) is becoming increasingly prevalent as a non-AIDS-defining cancer closely tied to chronic HIV infection. It is associated with increased secretion of inflammatory cytokines, immune system dysfunction, and alterations in mitochondrial function. The objective of this study was to investigate the levels of cytokine secretion and mitochondrial DNA (mtDNA) deletion in people living with HIV (PLWH) compared with individuals diagnosed with HCC without HIV.

A cross-sectional study was conducted with PLWH and HCC patients recruited from the Korle-Bu Teaching Hospital, Accra, Ghana. Participants donated whole blood for the isolation of plasma and peripheral blood mononuclear cells (PBMCs) for analysis. Cytokines were quantified in plasma samples using ELISA and Luminex techniques, while mtDNA deletions were determined with DNA extracted from the PBMCs.

The study found that the secretion of the cytokines TGF-β, FGF2, IL-8, TNF-α, VEGFA, and RANTES was similar in patients with HCC and PLWH. These cytokines have been implicated in HCC initiation and are also elevated in the early stages of the disease. Moreover, we observed comparably high levels of mtDNA deletion in PLWH and HCC patients.

These findings underscore the risks associated with HCC development in PLWH. There is a need for screening among PLWH, and these differentially expressed cytokines could serve as potential biomarkers.

The online version contains supplementary material available at 10.1186/s12876-025-04399-5.

## Linked entities

- **Proteins:** TGFB1 (transforming growth factor beta 1), FGF2 (fibroblast growth factor 2), CXCL8 (C-X-C motif chemokine ligand 8), TNF (tumor necrosis factor), VEGFA (vascular endothelial growth factor A), CCL5 (C-C motif chemokine ligand 5)
- **Diseases:** hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, CCL5 (C-C motif chemokine ligand 5) [NCBI Gene 6352] {aka D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228}
- **Diseases:** AIDS (MESH:D000163), HCC (MESH:D006528), HIV infection (MESH:D015658), cancer (MESH:D009369), inflammatory (MESH:D007249), immune system dysfunction (MESH:D007154)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12606890/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12606890/full.md

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Source: https://tomesphere.com/paper/PMC12606890