# N4BP1 is essential for the development of oral cancer via controlling both cancer cells and immune microenvironment

**Authors:** Yihua Song, Rong Sun, Jie Ji, Wen Zheng, Yanli Li, Xiaohong Guo, Liuting Chen, Yuanyuan Wu, Miaomiao Chen, Xingmei Feng, Mingbing Xiao, Renfang Mao, Yihui Fan

PMC · DOI: 10.1038/s41419-025-08229-0 · Cell Death & Disease · 2026-01-09

## TL;DR

N4BP1 promotes oral cancer by driving cancer cell growth and creating an immune-suppressive environment.

## Contribution

N4BP1 is newly identified as essential for oral cancer development through dual roles in cancer cells and immune regulation.

## Key findings

- N4BP1-deficient mice showed no visible tumors and prolonged survival in oral cancer models.
- N4BP1 regulates cancer cell proliferation and immune cell recruitment via CCL2 and GM-CSF.
- N4BP1 deficiency leads to M1 macrophage differentiation and reduced tumor progression.

## Abstract

N4BP1 specifically degrades a subset of mRNA targets through their coding sequences and functions as a negative regulator of inflammation; however, its role in cancer development remains undefined. N4BP1 exhibits the highest expression in head and neck squamous cell carcinoma among all analyzed cancer types. Unlike wild-type mice, N4bp1−/− mice did not develop visible tongue tumor masses in a 4-NQO-induced oral carcinogenesis model. Furthermore, N4bp1−/− mice (86% vs 0%) exhibited significantly prolonged survival compared to wild-type mice within 26 weeks in 4-NQO-induced oral carcinogenesis model. Single-cell profiling demonstrated that N4BP1-deficient epithelial cells arrest at an early stage of cancerous transformation, while wild-type epithelial cells efficiently progress to an advanced stage of cancer. In established human cancer cell lines, N4BP1 also plays a crucial role in proliferation, migration, colony formation, and in vivo growth. Transcriptome profiling identified CCL2 and GM-CSF as downstream targets of N4BP1 in oral cancer. Apart from its intrinsic role in cancer cells, N4BP1-deficient cancer cells induce the differentiation of macrophages into the M1 phenotype. In N4BP1-deficient tissues, CCL2 and GM-CSF were significantly increased, accompanied by the accumulation of M1 macrophages and neutrophils. Our results demonstrate that N4BP1 is an essential gene in tongue cancer development. N4BP1 not only drives cancer cell evolution but also establishes an immune-suppressive microenvironment. N4BP1 is an endoribonuclease that specifically regulates a subset of mRNA targets (including CCL2 and GM-CSF) and plays an essential role in oral cancer.

## Linked entities

- **Genes:** N4BP1 (NEDD4 binding protein 1) [NCBI Gene 9683], CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347], CSF2 (colony stimulating factor 2) [NCBI Gene 1437]
- **Chemicals:** 4-NQO (PubChem CID 5955)
- **Diseases:** oral cancer (MONDO:0023644), head and neck squamous cell carcinoma (MONDO:0010150)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Csf2 (colony stimulating factor 2 (granulocyte-macrophage)) [NCBI Gene 12981] {aka CSF, Csfgm, GMCSF, Gm-CSf, MGI-IGM}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 20296] {aka HC11, JE, MCAF, MCP-1, MCP1, SMC-CF}, N4bp1 (NEDD4 binding protein 1) [NCBI Gene 80750]
- **Diseases:** oral carcinogenesis (MESH:D063646), inflammation (MESH:D007249), cancer (MESH:D009369), tongue cancer (MESH:D014062), oral cancer (MESH:D009062), head and neck squamous cell carcinoma (MESH:D000077195)
- **Chemicals:** 4-NQO (MESH:D015112)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12789084/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12789084/full.md

---
Source: https://tomesphere.com/paper/PMC12789084