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. 2019 Mar 25;2019:8040361. doi: 10.1155/2019/8040361

Table 1.

Altered biomarkers in OC.

# Year Author Subjects (n) Sample origin Gene marker∗∗ Result P value
1 2010 Taoudi Benchekroun et al. 162 HB EGFR (U) An increased EGFR gene copy number increases the risk of OSCC P = 0.062
2 2012 Jung et al. 17 TB 134 different miRNA (see image 1) Keratinization and high miR-21 levels are important indicators of oral cancer patient prognosis P < 0.05
3 2013 Minakawa et al. 106 TB KIFGA (U) Results showed that KIFGA is overexpressed in OC P < 0.05
4 2015 Luo et al. 121 HB OPN (osteopontin) Tumor OPN plays an important role in tumor development particularly in tumor invasion and metastasis P = 0.002
5 2014 Su et al. 7 HB DEPDC1B (U) DEPDC1B is highly expressed in oral cancer tissue, compared to adjacent tissue. The overexpression in cells promotes cell migration and induces cell invasion in cancer cell lines /
6 2011 Cao et al. 76 TB EZM2(D) EZH2 expression is an independent predictor for OSCC. EZH2 may serve as a biomarker for oral cancer risk P = 0.05
7 2009 Saintigny et al. 162 HB deltaNp63 (U), EIC (U), podoplanin (U) Hazard risk of OC with upregulated genes is augmented. Considering all three biomarkers, OC patient survival rate is strikingly higher compared with no, one, or two positive biomarkers P < 0.0001
8 2011 Saintigny et al. 162 HB Has-miR-101 (D), deltaNp63 (U), P63 (U), DNMT3B (U) It demonstrated the value of gene expression profiles in predicting oral cancer development in OPL patients. The microRNA-based strategies might therefore be considered in future chemoprevention studies /

Type of sample: HU: human biopsy; TB: tissue bank sample. ∗∗Type of altered gene regulation: D: downregulation, diminution; U: upregulation, augmentation.