Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
0.380 | AlteredExpression | disease | BEFREE | Furthermore, EGFR was significantly upregulated in TSCC tissues, and the levels of miR‑509 were revealed to be negatively correlated with EGFR expression in TSCC tissues. | 28944863 | 2017 | ||||
|
0.380 | AlteredExpression | disease | BEFREE | Elevated pEGFR protein expression was significantly more frequently observed in mobile tongue SCC cases with a well-defined tumor shape and an earlier disease stage (P = .010 and P = .019, respectively). | 27657462 | 2017 | ||||
|
0.380 | AlteredExpression | disease | BEFREE | These results suggested that ADAM10 is important in regulating the proliferation, invasion and migration of the human tongue squamous cell carcinoma cell line TCA8113 and that the mechanism may, at least in part, be associated with the upregulation of EGFR and the downregulation of E-cadherin. | 25333745 | 2015 | ||||
|
0.380 | Biomarker | disease | BEFREE | The immunohistochemical study using the surgical specimens in 52 patients with tongue SCC also showed a significant correlation between SGLT1 and EGFR. | 21607591 | 2012 | ||||
|
0.380 | Biomarker | disease | BEFREE | These results suggest that HER-1 and HER-2/neu when determined with stringent criteria are not useful indicators of prognosis in SCCT. | 19691460 | 2010 | ||||
|
0.380 | Biomarker | disease | BEFREE | Human SCC of the tongue Tca8113 cells were treated with AG1478 to block EGFR signalling, and were transfected with the vector that encodes the specific short hairpin RNA (shRNA) that targets EGFR. | 19398252 | 2010 | ||||
|
0.380 | AlteredExpression | disease | BEFREE | EGFR protein overexpression and gene copy number increases in oral tongue squamous cell carcinoma. | 19332367 | 2009 | ||||
|
0.380 | GeneticVariation | disease | BEFREE | EGFR mutations and human papillomavirus in squamous cell carcinoma of tongue and tonsil. | 17224267 | 2007 | ||||
|
0.380 | CausalMutation | disease | CGI |