# Roles of E3 ubiquitin ligases and deubiquitinating enzymes in renal cell carcinoma

**Authors:** Minshu Jiang, Wenxia Si, Sien Huang, Sha Qu, Minghui Zhang, Yi Quan

PMC · DOI: 10.3389/fonc.2025.1628710 · Frontiers in Oncology · 2026-01-21

## TL;DR

This paper reviews how E3 ubiquitin ligases and deubiquitinating enzymes affect kidney cancer development and treatment.

## Contribution

The paper provides a comprehensive review of E3 and DUB enzymes' roles in RCC and their therapeutic potential.

## Key findings

- E3 ubiquitin ligases and DUBs regulate protein stability and signaling in RCC.
- Targeting these enzymes may offer new therapeutic strategies for RCC.
- Their molecular mechanisms in RCC are increasingly understood.

## Abstract

Ubiquitination is an important post-translational modification of proteins that precisely regulates protein stability and function through the coordinated actions of E3 ubiquitin ligases (E3s) and deubiquitinases (DUBs), participating in biological processes including protein degradation and signal transduction. In recent years, the role of ubiquitination modification in the carcinogenesis, progression, and treatment of renal cell carcinoma (RCC) has garnered increasing attention. This review summarizes the structural classifications of key enzymes in the ubiquitination process—E3s and DUBs—and to discuss their specific molecular mechanisms in RCC. Finally, we discuss the targeted therapeutic strategies focusing on these key ubiquitination-modifying enzymes in RCC.

## Linked entities

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

## Full-text entities

- **Diseases:** RCC (MESH:D002292), carcinogenesis (MESH:D063646)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12867792/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12867792/full.md

## References

126 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867792/full.md

---
Source: https://tomesphere.com/paper/PMC12867792