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Table 3 Genomic substance

From: Current concepts and future of noninvasive procedures for diagnosing oral squamous cell carcinoma - a systematic review

Genome

Functions

Type of abnormality

Reported rate in the saliva

Mitochondrial DNA

 

mutations

67%

p53 gene: Tumor-suppressor genes

Cell-cycle regulation Senescence, cell-cycle progression

mutations

71%

p16* : Tumor-suppressor genes

Cell-cycle regulation Senescence, cell-cycle progression

Hypermethylation

47%

DAP-K*

kinase whose expression is required for IFN-γ-induced apoptosis

Hypermethylation

33%

MGMT*

 

Hypermethylation

23%

CDKN2A

Control of cell cycle, arrest cell cycle at G1& G2act like a Tumor-suppressor genes

Hypermethylation

30.2%

CDH1

Encodes Ca++ dependent cell to cell adhesions

Hypermethylation

-

c-MYCIN: Proto-oncogenes

Cell growth, apoptosis

amplification

20-40%

Cyclin D oncogenes: Proto-oncogenes

Cell-cycle regulation

amplification

87%

  1. *p16, MGMT,DAP-K (methylation of at least one of these genes in 65%).