# Identification of actin cytoskeleton organization genes in oral cancer and oral potentially malignant disorders using oral tissue RNA-seq database

**Authors:** Marta Serna-García, Agnese Formaggio, María Carmen Carceller, Joaquín Javier Panadero Romero, Nicla Flacco

PMC · DOI: 10.4317/medoral.27364 · Medicina Oral, Patología Oral y Cirugía Bucal · 2025-08-16

## TL;DR

This study identifies genes related to actin cytoskeleton organization that are linked to oral cancer and potentially malignant disorders, suggesting their potential as early biomarkers and therapeutic targets.

## Contribution

The study identifies key actin-related genes associated with oral cancer and potentially malignant disorders using RNA-seq data and validates their potential as biomarkers.

## Key findings

- EPRS1 was consistently overexpressed in oral cancer, leukoplakia, and oral submucous fibrosis.
- Genes like ACTIN1, LIMK1, and others were linked to actin cytoskeleton organization and cancer progression.
- ROC analysis on TCGA data showed these genes' potential as early biomarkers for oral cancer.

## Abstract

Oral cancer and oral potentially malignant disorders (leukoplakia and oral submucous fibrosis) are prevalent and clinically significant oral diseases. Actin, crucial for epithelial tissue integrity, undergoes cytoskeleton reorganization associated with increased invasiveness in oral cancer.

Bioinformatic analysis of RNA-seq data from GEO public databases was performed to detect differentially expressed genes in oral cancer, leukoplakia and oral submucous fibrosis. Enrichment analysis of the differentially expressed genes was performed using DAVID and GSEA software. ROC curve and survival analysis were conducted to assess the discriminative capacity of these genes as possible biomarkers. The results were further validated using RNAseq data from The Cancer Genome Atlas (TCGA).

EPRS1 was consistently overexpressed in all three pathologies. Key genes (ACTIN1, LIMK1, CORO1C, INF2, SH3D21, CFL1, FSCN1, MYO1B) implicated in actin cytoskeleton organization were identified, suggesting their role in oral potentially malignant disorders and cancer progression. Receiver operating characteristic (ROC) curves on 522 TCGA samples demonstrated these genes' potential as early biomarkers for oral cancer, with their inhibition associated with improved survival.

The identified genes offer insights into actin-related mechanisms and potential pathways for the diagnosis and treatment of oral cancer. Nonetheless, further research is essential to validate these results.

Key words:RNA-seq, oral cancer, oral submucous fibrosis, leukoplakia, actin.

## Linked entities

- **Genes:** EPRS1 (glutamyl-prolyl-tRNA synthetase 1) [NCBI Gene 2058], ACT1 (actin 1) [NCBI Gene 818339], LIMK1 (LIM domain kinase 1) [NCBI Gene 3984], CORO1C (coronin 1C) [NCBI Gene 23603], INF2 (inverted formin 2) [NCBI Gene 64423], MNMIP1 (manchette microtubule inner protein 1) [NCBI Gene 79729], CFL1 (cofilin 1) [NCBI Gene 1072], FSCN1 (fascin actin-bundling protein 1) [NCBI Gene 6624], MYO1B (myosin IB) [NCBI Gene 4430]
- **Diseases:** oral cancer (MONDO:0023644), leukoplakia (MONDO:0043243), oral submucous fibrosis (MONDO:0018166)

## Full-text entities

- **Genes:** FSCN1 (fascin actin-bundling protein 1) [NCBI Gene 6624] {aka HSN, SNL, p55}, CFL1 (cofilin 1) [NCBI Gene 1072] {aka CFL, HEL-S-15, cofilin}, MNMIP1 (manchette microtubule inner protein 1) [NCBI Gene 79729] {aka C1orf113, SH3D21}, MYO1B (myosin IB) [NCBI Gene 4430] {aka MMI-alpha, MMIa, MYH-1c, myr1}, CORO1C (coronin 1C) [NCBI Gene 23603] {aka HCRNN4}, LIMK1 (LIM domain kinase 1) [NCBI Gene 3984] {aka LIMK, LIMK-1}, INF2 (inverted formin 2) [NCBI Gene 64423] {aka C14orf151, C14orf173, CMTDIE, FSGS5, pp9484}
- **Diseases:** oral potentially malignant disorders (MESH:C537245), oral diseases (MESH:D009059), leukoplakia (MESH:D007971), Cancer (MESH:D009369), oral submucous fibrosis (MESH:D009914), Oral cancer (MESH:D009062)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12579942/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12579942/full.md

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Source: https://tomesphere.com/paper/PMC12579942