Oral
squamous cell carcinoma (OSCC) is the most common cancer in
the oral and maxillofacial region. Due to the special physiological
and anatomical position of the oral cavity, the disease often has
a significant impact on the chewing, swallowing, language, and breathing
functions of patients. In recent years, with the development of medical
molecular biology, molecular targeted therapy has received increasing
clinical attention and has gradually become a new method for the treatment
of malignant tumors. In this research, gold nanostars with a high
photothermal effect combined with the searched targeted antibody were
used for OSCC therapy. We use the data set in the public database
and construct a gene co-expression module by weighted gene co-expression
network analysis (WGCNA). It was found that the turquoise module and
the midnight blue module had the greatest connection to tumorigenesis.
Cytoscape software was used to analyze the important modules, and
the top 10 genes of each module were selected; the survival analysis
of the top 10 genes was carried out by gene expression profiling interactive
analysis (GEPIA), which indicated that these genes (SERPINH1,
MMP11, ADAM12, FADS3, SLC36A2, C1QTNF7, SCRG1, and APOBEC2) have statistical
significance as key genes that are related to the tumorigenesis of
OSCC. Then, the anti-SERPINH1 antibody targeted to SERPINH1
was chosen as the inhibitor and combined with gold nanostars for photothermal
assisted targeted therapy. Thus, the searched key genes can be regarded
as biomarkers and therapeutic targets for further precise diagnosis.