# Gastric metastasis of renal cell carcinoma: features, mechanisms, and insights from existing literature

**Authors:** Xiaoqian Wang, Luling Wei, Runchang Liu, Xuezhe Wang, Xinchi Luan, Xiaoxuan Li, Haoran An, Ruizhe Zhao, Yue Qiu

PMC · DOI: 10.3389/fcell.2025.1656858 · 2025-10-15

## TL;DR

This paper reviews the features and mechanisms of gastric metastasis in kidney cancer, highlighting challenges and potential treatment strategies.

## Contribution

The paper provides a comprehensive review of gastric metastasis in renal cell carcinoma, integrating mechanisms and therapeutic insights.

## Key findings

- Gastric metastases from RCC are rare, occur years after surgery, and have a poor prognosis.
- Dysregulated pathways like PI3K/AKT and Wnt/β-catenin drive metastasis and tumor adaptation in the gastric environment.
- Emerging multi-omics and single-cell sequencing may improve understanding and treatment of organ-specific metastasis.

## Abstract

Renal cell carcinoma (RCC), a malignancy characterized by an increasing global incidence, exhibits a tendency for metastatic dissemination. However, gastric metastases, often identified in multicenter case series with an incidence of 0.2%–0.8%, typically present years after nephrectomy (median interval ∼6.7 years) and are associated with a poor prognosis (5-year OS ∼21% in historical cohorts). Gastric metastases typically present years after nephrectomy as either isolated or polymetastatic lesions, often accompanied by severe upper gastrointestinal symptoms and presenting significant clinical challenges. Mechanistically, the progression of metastasis is driven by dysregulated signaling pathways, including PI3K/AKT, Ras/MAPK, and Wnt/β-catenin, which facilitate epithelial-mesenchymal transition (EMT), extracellular matrix (ECM) remodeling, and angiogenesis. The gastric microenvironment further contributes to tumor adaptation through metabolic stress, immune evasion, and exosome-mediated intercellular communication. Clinically, oligometastatic disease may benefit from surgical resection in combination with immunotherapy, whereas polymetastatic cases necessitate systemic therapies such as tyrosine kinase inhibitors and immune checkpoint blockers, albeit with limited efficacy. Emerging multi-omics approaches and single-cell sequencing technologies hold promise for elucidating organ-specific tropism and refining personalized treatment strategies. This review highlights the critical need to integrate mechanistic insights with innovative therapeutic interventions to improve outcomes for patients with gastric metastasis of RCC.

## Linked entities

- **Diseases:** renal cell carcinoma (MONDO:0005086)

## Full-text entities

- **Genes:** CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** Gastric metastases (MESH:D009362), malignancy (MESH:D009369), RCC (MESH:D002292)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12572941/full.md

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Source: https://tomesphere.com/paper/PMC12572941