Table 1.
Intrinsic and cell surface factors associated with HNSCC pathogenesis.
Function | Factors | Refs. no in foot note |
---|---|---|
1. Agonist dependent or independent signal transduction | EGFR, erbB2 (HER2), PDGFR, IGFR, c‐Met, src, Ras, Stat3, MAPK, NF‐κB, PI3K‐PTEN‐AktmTOR, Wnt/β‐catenin, TGF‐β/smad, CXCR, p38, CIN85 | 1 |
2. DNA replication and repair | p53, nucleotide excision repair (NER), OGG | 2 |
3. Genetic and chromosomal instability | chromosomal number variation, DNA aneuploidy, LOH, SNP, chromosomal rearrangemen, | 3 |
4. Cell fate, survival, differentiation, senescence, and apoptosis | Telomerase, Survivin, Bcl‐2/XL, Bax, IAPs, p53, Myc | 4 |
5. Mitotic regulation | aurora kinase A | 5 |
6. Cell cycle and check point control | cyclin D1, p14, p16, p21, p27, pRB, CDC25A,CDC25B | 6 |
7. Cell adhesion and motility | integrins, E‐cadherin, CD44, moesin, laminin | 7 |
8. Transcription, translation post‐translation regulation and chromatin remodeling | DNA methylation, miRNA, eIF4, S6, HSP, BMI1, EZH2 | 8 |
9. Viral infection | human papilloma virus, Epstein–Barr virus | 9 |
10. Intracellular metabolism | aerobic glycolysis (Warburg effect), hypoxia, xenobiotics, prostaglandin synthesis, Cox‐2, reactive oxygen species (ROS), HIF‐1, mitochondrial DNA mutation, PDK1, LDH, TKLT‐1, Myc, AktmTOR | 10 |
11. Epithelial–mesenchymal transition | Src, BMI1, ZEB1, TrkB, Cox‐2, HMGA2, IL‐1β, Snail, Twist, E‐cadherin, Vimentin | 11 |
12. Cancer stemness | CD44, Notch, Wnt, Oct, Nanog, Stat3, CD133, ALDH1 | 12 |
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