Transcriptome Analysis of Oral Submucous fibrosis and its Malignant Transformation

High-throughput RNA sequencing was performed on fresh de novo OSCC samples (n=8), OSMF transforming to OSCC, and normal oral mucosa (n=5 each) using Illumina-compatible NEXTflex Rapid Directional RNA-Sequencing. Results: Upregulated genes were associated with cytokine and immune responses (ABRA, TTTY14, EIF1AY), cellular proliferation and apoptosis (LINC00314, RPS4Y1, SERPINA5, TRIM63, FABP7), and energy metabolism, indicating metabolic adaptations during malignant progression.

Pathway analysis showed increased expression of TNNT1, TNNI1, MYL4, and ACTN3, implicating muscle development and embryonic pathways in OSMF transformation. Conversely, genes related to epithelial differentiation and keratinization (FLG, FLG2, HRNR, TCHH, KRT73), immune regulation and tumor suppression (HLA-G, UNC5D), and metabolic signaling were downregulated, reflecting loss of tissue integrity and immune control. Conclusion: The observed gene dysregulation highlights impaired epithelial barrier function, altered immune responses, and enhanced metastatic potential, contributing to carcinogenesis and poor prognosis in OSMF-associated OSCC.