Exploration of the Important Role of Microfibril-Associated Protein 4 Gene in Oral Squamous Cell Carcinoma

Ying Han1, Kun Xia1, Tong Su2,3,4

  • 1Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China (mainland).

Insights

Microfibril-associated protein 4 (MFAP4) shows decreased expression in oral squamous cell carcinoma (OSCC) tumors. Higher MFAP4 levels correlate with better patient prognosis, suggesting its potential as a prognostic biomarker for OSCC risk stratification.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genomics

Background:

  • Oral squamous cell carcinoma (OSCC) is a prevalent head and neck cancer requiring multimodal treatment.
  • Current treatment strategies lack specific molecular biomarkers for guidance.
  • Microfibril-associated protein 4 (MFAP4) has shown potential in disease assessment, but its role in tumors is unexplored.

Purpose of the Study:

  • To investigate microfibril-associated protein 4 (MFAP4) as a novel prognostic biomarker for oral squamous cell carcinoma (OSCC).
  • To analyze the relationship between MFAP4 expression and key tumor characteristics, including mutation burden, miRNA regulation, and immune cell infiltration.

Main Methods:

  • Utilized Gene Expression Omnibus (GEO) datasets (GSE25099, GSE30784) for OSCC patient data.
  • Compared MFAP4 gene expression between normal and tumor tissues using the UCSC Xena browser.
  • Analyzed associations between MFAP4 expression levels and tumor mutation burden (TMB), miRNA regulation, and immune cell infiltration.

Main Results:

  • MFAP4 gene expression was significantly downregulated in OSCC tumors compared to normal tissues.
  • High MFAP4 expression was associated with improved patient prognosis.
  • MFAP4 expression showed potential correlations with TMB, miRNA regulation, and immune cell infiltration patterns.

Conclusions:

  • MFAP4 serves as a promising prognostic biomarker for risk stratification in OSCC patients.
  • MFAP4 expression is linked to the regulation of tumor mutation burden, microRNAs, and immune cell infiltration in OSCC.

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