“…Genetic alterations, such as the change of gene expressions of tumor suppressor genes and oncogenes, also play important roles in the development of OSCC [5]. A few review articles [6][7][8][9] summarized genetic anomalies associated with OSCC according to the type of structure affected (chromosome, allele, oncogene, tumor suppressor gene, or nucleotide) and the type of anomaly (polymorphism, point mutation, deletion, and other alterations). Many OSCC-associated genes (e.g., TP53, CDKN2A, Cyclin D1, EGFR, SMAD-2, SMAD-4, CDK2AP1, FHIT) have been identified [4,7,8,10].…”