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Updated: Jul 4, 2025

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Transcriptomic Profiling of OSCC Patients in an Indian Subset
Amisha Patel1, Alpesh Kikani2, Gautam Makadiya2
1Department of Microbiology, School of Science, RK University, Rajkot, Gujarat, India.
This study identified novel molecular biomarkers for oral squamous cell carcinoma (OSCC) through transcriptome profiling. These biomarkers can improve early detection and therapeutic strategies for OSCC patients.
Area of Science:
- Oncology
- Genomics
- Biomarker Discovery
Background:
- Tumor-specific biomarkers are crucial for early detection, prognosis, and therapeutic strategy design in cancer.
- Comprehensive transcriptome profiling provides insights into disease mechanisms and potential drug targets.
Purpose of the Study:
- To identify novel molecular biomarkers for oral squamous cell carcinoma (OSCC).
- To explore potential therapeutic targets for improved cancer prognosis and early diagnosis.
Main Methods:
- Transcriptome sequencing was performed on 5 pairs of cancerous and normal oral tissues from OSCC patients.
- Gene expression analysis was conducted using Roche's 454 sequencing platform and CLC Genomics Workbench.
- Gene enrichment and pathway analysis were performed using Topfunn, along with protein-protein interaction (PPI) network construction.
Main Results:
- 2082 differentially expressed genes were identified in OSCC tissues, including 1092 upregulated and 273 downregulated genes.
- Pathway analysis revealed significant involvement of TNF signaling, p53 signaling, cGMP-PKG signaling, Apelin signaling, and IL-17 signaling in tumor cell proliferation and apoptosis.
- A PPI network identified 8 key protein interactions.
Conclusions:
- The study identified potential molecular biomarkers (INHBA, FJX1, OLR1, CDK2, IGHM, CXCL11, SH2D5, FABP5) associated with OSCC.
- These biomarkers may serve as therapeutic targets for better prognosis and can enhance early diagnostic accuracy in clinical practice.
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