# PSMB8 as a Core Target Mediating the Anti-Hepatocellular Carci-Noma Activity of Lingonberry (Vaccinium vitis-idaea L.) Extract in HepG2 Cells

**Authors:** Liangyu Zhu, Zhi Zhang, Yandong Zhang, Dianwen Wei, Zhenyu Wang, Liping Zhou

PMC · DOI: 10.3390/cimb48030323 · 2026-03-18

## TL;DR

Lingonberry extract shows anti-cancer effects in liver cancer cells by targeting PSMB8, offering a potential new treatment approach.

## Contribution

Identifies PSMB8 as a core target mediating the anti-HCC activity of Lingonberry extract.

## Key findings

- PSMB8 was identified as a core regulatory gene in HepG2 cells treated with Lingonberry extract.
- Downregulating PSMB8 induces late apoptosis in HepG2 cells.
- Lingonberry extract significantly reduces PSMB8 protein expression.

## Abstract

Hepatocellular carcinoma (HCC) is a highly malignant tumour with a poor prognosis and few effective treatment options. Development of resistance to conventional therapies and occurrence of severe side effects highlight the urgent need for novel, low-toxicity interventions. Natural products are promising candidates for HCC drug development thanks to their multi-target activity and favourable safety profiles. Previous studies reported that Lingonberry extract, a bioactive natural product, inhibits proliferation of HepG2 cells. However, the key molecular targets and underlying anticancer mechanisms remain unclear. In this study, we analysed gene chip data from Lingonberry extract-treated HepG2 tumour-bearing mice using bioinformatics tools, employing a cross-species, multi-level screening strategy to identify PSMB8 as the core regulatory gene. In vitro functional validations (Western blotting, RT-PCR, CCK-8 assay, colony formation assay, flow cytometry and TUNEL staining) confirmed these findings. Downregulating PSMB8 was found to effectively induce late apoptosis in HepG2 cells, and Lingonberry extract was found to significantly reduce PSMB8 protein expression. This study identifies PSMB8 as a key mediator of the anticancer effect of Lingonberry extract in HepG2 cells. It provides a reliable methodological reference for screening anticancer targets of natural products and supports further exploration of Lingonberry extract as a potential adjuvant/lead compound for HCC.

## Linked entities

- **Genes:** PSMB8 (proteasome 20S subunit beta 8) [NCBI Gene 5696]
- **Diseases:** Hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)

## Full-text entities

- **Genes:** PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, NOTCH1 (notch receptor 1) [NCBI Gene 4851] {aka AOS5, AOVD1, TAN1, hN1}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, PSMB8 (proteasome 20S subunit beta 8) [NCBI Gene 5696] {aka ALDD, D6S216, D6S216E, JMP, LMP7, NKJO}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, FOLH1B (folate hydrolase 1B (pseudogene)) [NCBI Gene 219595] {aka FOLH2, FOLHP, PSM, PSMA-LIKE, PSMAL}, ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}, ZNF655 (zinc finger protein 655) [NCBI Gene 79027] {aka VIK, VIK-1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** liver fibrosis (MESH:D008103), inflammatory (MESH:D007249), mycoplasma (MESH:D009175), lipid (MESH:D011017), liver injury (MESH:D017093), necrotic (MESH:D009336), Tumour (MESH:D009369), weight loss (MESH:D015431), dislocation (MESH:D004204), malignant melanoma (MESH:D008545), toxicities (MESH:D064420), HCC (MESH:D006528), inflammatory response (MESH:D018746), metastasis (MESH:D009362), non-alcoholic fatty liver disease (MESH:D065626), Infections (MESH:D007239), injury (MESH:D014947)
- **Chemicals:** Malvidin-3-galactoside (MESH:C458399), sorafenib (MESH:D000077157), CCl4 (MESH:D002251), saline (MESH:D012965), nitrogen (MESH:D009584), flavonoids (MESH:D005419), cyclophosphamide (MESH:D003520), CO2 (MESH:D002245), polyphenols (MESH:D059808), bevacizumab (MESH:D000068258), Penicillin (MESH:D010406), atezolizumab (MESH:C000594389), lenvatinib (MESH:C531958), lipid (MESH:D008055), MDA (MESH:D015104), resveratrol (MESH:D000077185), Propidium Iodide (MESH:D011419), paraformaldehyde (MESH:C003043), DAPI (MESH:C007293), SDS (MESH:D012967), polyamide (MESH:D009757), Triton X-100 (MESH:D017830), crystal violet (MESH:D005840), ethanol (MESH:D000431), anthocyanin (MESH:D000872), ellagic acid (MESH:D004610), streptomycin (MESH:D013307), Curcumin (MESH:D003474), PVDF (MESH:C024865), phenolic acids (MESH:C017616), DMEM (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Vaccinium vitis-idaea (cowberry, species) [taxon 180772], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), IGR39 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_2076), BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), CCK-8 — Homo sapiens (Human), T-cell prolymphocytic leukemia, Cancer cell line (CVCL_5443), 293T — Homo sapiens (Human), Transformed cell line (CVCL_0063)

## Figures

18 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13025438/full.md

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Source: https://tomesphere.com/paper/PMC13025438