# Traditional Chinese medicine prescription Guizhi Fuling Pills ameliorate cisplatin-induced renal injury via remodeling intestinal homeostasis in mice with tongue squamous cell carcinoma

**Authors:** Kai Fu, Shaoning Yin, Tengfei Liu, Weiyi Wang

PMC · DOI: 10.3389/fphar.2025.1631966 · Frontiers in Pharmacology · 2025-10-02

## TL;DR

This study shows that Guizhi Fuling Pills help reduce kidney damage from cisplatin in mice with tongue cancer by improving gut health.

## Contribution

The study reveals a novel mechanism by which Guizhi Fuling Pills protect the kidneys through gut microbiota modulation during cancer treatment.

## Key findings

- Guizhi Fuling Pills reduced cisplatin-induced kidney injury by lowering CRE, BUN, MDA, and TNF-α levels.
- The treatment improved gut health by increasing beneficial bacteria and goblet cells while decreasing harmful species.
- The combination therapy maintained anti-tumor efficacy against tongue squamous cell carcinoma.

## Abstract

Guizhi Fuling Pills, a traditional Chinese medicine, may affect cisplatin-induced kidney damage during tongue squamous cell carcinoma (TSCC) treatment via the gut–kidney axis, but this is not well understood. This study explores the impact of Guizhi Fuling Pills on gut microbiota and intestinal barrier function, its protective effects against cisplatin-induced kidney injury, and the mechanisms involved.

A tongue tumor model was created in nude mice using Cal27 cells. Treatments included cisplatin, Guizhi Fuling Pills, or both. Kidney function was evaluated through serum creatinine (CRE) and blood urea nitrogen (BUN). Oxidative stress and inflammation were assessed by measuring malondialdehyde (MDA), superoxide dismutase (SOD) activity, and tumor necrosis factor-α (TNF-α). Gut microbiota was analyzed via 16S rRNA sequencing, and intestinal morphology was examined using H&E and PAS staining.

The coadministration of Guizhi Fuling Pills with DDP demonstrated multifaceted effects. At the systemic level, it ameliorated renal pathological changes, as evidenced by decreased serum levels of CRE, BUN, MDA, and TNF-α, alongside increased SOD activity. It also enhanced the inhibitory effect on TSCC tumor growth. In the gut, this combination reduced crypt depth, increased goblet cell number, and favorably modulated the microbiota by decreasing the abundance of Desulfovibrioand increasing beneficial bacteria including Lactobacillus, Kineothrix, and Eubacterium, without affecting ZO-1 expression.

Guizhi Fuling Pill effectively mitigates cisplatin-induced renal injury and maintains its anti-tumor efficacy in TSCC by modulating gut microflora and reducing inflammation.

## Linked entities

- **Chemicals:** cisplatin (PubChem CID 5460033), malondialdehyde (PubChem CID 10964)
- **Diseases:** tongue squamous cell carcinoma (MONDO:0000500)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** kidney damage (MESH:D007674), inflammation (MESH:D007249), TSCC (MESH:D000077195), tumor (MESH:D009369), renal pathological (MESH:D002114), tongue tumor (MESH:D014062)
- **Chemicals:** DDP (MESH:D002945), Guizhi Fuling Pill (-), MDA (MESH:D008315), CRE (MESH:D003404)
- **Species:** Lactobacillus (genus) [taxon 1578], Eubacterium (genus) [taxon 1730], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** Cal27 — Homo sapiens (Human), Tongue adenosquamous carcinoma, Cancer cell line (CVCL_1107)

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12528071/full.md

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Source: https://tomesphere.com/paper/PMC12528071