# Targeting MDM2, RAS, and PCNA for cancer targeted therapy: pan-cancer approaches vs. cancer-specific strategies

**Authors:** Wei Wang, Abigail Alley, Na Sun, Meheret Tadesse, Xinshi Wang, Ruiwen Zhang

PMC · DOI: 10.3389/fphar.2025.1663766 · Frontiers in Pharmacology · 2025-10-15

## TL;DR

This paper reviews pan-cancer and cancer-specific strategies for targeting RAS, PCNA, and MDM2 to improve cancer therapy.

## Contribution

It emphasizes the potential of biomarker-driven pan-cancer approaches using these targets to reshape cancer treatment.

## Key findings

- RAS, PCNA, and MDM2 are key molecular drivers with broad roles in cancer biology.
- Pan-cancer strategies targeting these proteins offer new therapeutic opportunities.
- Challenges like drug resistance and tumor heterogeneity remain significant obstacles.

## Abstract

Cancer therapy and cancer drug discovery and development have been historically focused on specific cancers (tissue/organ of origin). However, with advances in molecular biology and multi-omics of cancer, there is a trend to develop pan-cancer therapeutic modalities. In targeted therapy, pan-cancer strategies target common molecular alterations across different cancer types and specific cancer strategies are tailored to the unique biological characteristics of individual tumor types. Each approach offers distinct advantages and limitations, and understanding these differences is critical in the era of precision oncology. Targeting key molecular drivers in cancer has significantly changed drug development, allowing for broad-spectrum therapeutic strategies that address shared oncogenic pathways across various tumor types. Among these drivers, RAS, PCNA, and MDM2 have become critical targets due to their roles in a broad-spectrum of cancer biology, e.g., cell proliferation, survival, and genomic stability. Advances in molecularly guided therapies have led to promising approaches for disrupting these pathways, offering new opportunities for cancer treatment. Despite significant progress in the past, challenges such as drug resistance, tumor heterogeneity, and toxicity remain obstacles to widespread clinical success. This review explores the historical development, current advancements, and future directions of RAS, PCNA, and MDM2-targeted therapies, emphasizing their potential to reshape cancer treatment through pan-cancer approaches using biomarker-driven technologies, combination strategies, and next-generation inhibitors. These advancements pave the way for more effective and durable therapies across a wide range of malignancies.

## Linked entities

- **Genes:** ras (resistance to audiogenic seizures) [NCBI Gene 19412], PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111], MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193]

## Full-text entities

- **Genes:** MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193] {aka ACTFS, HDMX, LSKB, hdm2}, PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111] {aka ATLD2}
- **Diseases:** Cancer (MESH:D009369), toxicity (MESH:D064420)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12568505/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12568505/full.md

## References

268 references — full list in the complete paper: https://tomesphere.com/paper/PMC12568505/full.md

---
Source: https://tomesphere.com/paper/PMC12568505