Molecular biology of oral cavity squamous cell carcinoma

Oral Oncol. 2020 Mar:102:104552. doi: 10.1016/j.oraloncology.2019.104552. Epub 2020 Jan 7.

Abstract

Oral cavity squamous cell carcinoma (OCSCC) is a heterogeneous and complex disease that arises due to dysfunction of multiple molecular signaling pathways. Recent advances in high-throughput genetic sequencing technologies coupled with innovative analytical techniques have begun to characterize the molecular determinants driving OCSCC. An understanding of the key molecular signaling networks underlying the initiation and progression of is essential for informing treatment of the disease. In this chapter, we discuss recent findings of key genes altered in OCSCC and potential treatments targeting these genes.

Keywords: Cancer genetics; Epigenetics; HNSCC; Head and neck cancer; Head and neck squamous cell carcinoma; Immunotherapy; Molecular biology of oral cavity squamous cell carcinoma; Oral cancer; Oral cavity cancer; Squamous cell carcinoma.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / therapy
  • Cyclin D1 / genetics
  • Cyclin D1 / metabolism
  • Cyclin-Dependent Kinase Inhibitor p16 / genetics
  • Cyclin-Dependent Kinase Inhibitor p16 / metabolism
  • Epigenesis, Genetic
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Immunotherapy
  • Mouth Neoplasms / genetics*
  • Mouth Neoplasms / metabolism
  • Mouth Neoplasms / pathology
  • Mouth Neoplasms / therapy
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Oncogene Protein v-akt / genetics
  • Oncogene Protein v-akt / metabolism
  • Phosphatidylinositol 3-Kinase / genetics
  • Phosphatidylinositol 3-Kinase / metabolism
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism
  • Retinoblastoma Protein / genetics
  • Retinoblastoma Protein / metabolism
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism
  • beta Catenin / genetics
  • beta Catenin / metabolism

Substances

  • CCND1 protein, human
  • CTNNB1 protein, human
  • Cyclin-Dependent Kinase Inhibitor p16
  • NOTCH1 protein, human
  • Neoplasm Proteins
  • Receptor, Notch1
  • Retinoblastoma Protein
  • Tumor Suppressor Protein p53
  • beta Catenin
  • Cyclin D1
  • MTOR protein, human
  • Phosphatidylinositol 3-Kinase
  • ErbB Receptors
  • Oncogene Protein v-akt
  • TOR Serine-Threonine Kinases