Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE This study investigated the immunohistochemical expression of retinoblastoma (RB) protein and p16 protein in 10 neuroendocrine carcinomas (NECs), in comparison to two mixed-type NECs; 28 squamous cell carcinomas (SCCs), and 12 carcinosarcomas (CSs) from patients with esophageal cancer. 30952735 2019
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 AlteredExpression group BEFREE SNHG7 can partly promote the development of esophageal cancer by regulating the expression of p15 and p16. 29771415 2018
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE Epigallocatechin-3-gallate inhibits growth and induces apoptosis in esophageal cancer cells through the demethylation and reactivation of the p16 gene. 28693288 2017
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE Our findings indicate that CDKN2A methylation has a vital role in EC tumorigenesis and could be a biomarker for early diagnosis of EC. 28637022 2017
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE The p53 expression was positive in 67.5% of tumor tissue, 20.0% of adjacent non-tumoral tissue and 1.8% of normal esophageal tissue. p16 was positive in 11.6% of esophageal cancer cases and 4.7% of adjacent non-tumoral tissue. p16 was undetectable among control group samples. p53 and p16 levels were not significantly associated with the HPV status. 28529620 2017
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 GeneticVariation group BEFREE Hypermethylation of p16 gene was not found in healthy controls. p53 Pro/Pro genotype was found to be a risk genotype in Northeast India compared with Arg/Pro and Arg/Arg. p53 variant/polymorphism was significantly associated with esophageal cancer risk in the study population under all three genetic models, namely, dominant model (Arg/Pro + Pro/Pro vs Arg/Arg odds ratio = 2.25, confidence interval = 1.19-4.26; p = 0.012), recessive model (Arg/Arg + Arg/Pro vs Pro/Pro odds ratio = 2.35, confidence interval = 1.24-4.44; p = 0.008), and homozygous model (Pro/Pro vs Arg/Arg odds ratio = 3.33, confidence interval = 1.54-7.20; p = 0.002). 28459370 2017
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 AlteredExpression group BEFREE HPV infection and p53 and p16 expression in esophageal cancer: are they prognostic factors? 29046713 2017
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE Low expression of (or IHC-negative) COX2, miR-200c, ERCC1 and TS, or high expression of (or IHC-positive) CDC25B and p16 are potential biomarkers for predicting the response of esophageal cancer patients treated with chemo(radio)therapy. 29113666 2017
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 PosttranslationalModification group BEFREE Betel quid and tobacco chewing habit synergistically with p16 methylation elevated the risk for esophageal cancer development (adjusted odds ratio (OR) = 6.88, 95% confidence interval (CI) = 1.64-28.81, p = 0.003 for betel quid chewing and adjusted OR = 7.02, 95% CI = 1.87-26.38, p = 0.001 for tobacco chewing). 25361631 2015
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 PosttranslationalModification group BEFREE The aim of this study is to offer a systematic review on the aberrant methylation of p16 gene in esophageal cancer. 24240582 2013
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 PosttranslationalModification group BEFREE Associations of risk factors obesity and occupational airborne exposures with CDKN2A/p16 aberrant DNA methylation in esophageal cancer patients. 20459442 2010
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group CTD_human Progressive silencing of p14ARF in oesophageal adenocarcinoma. 18410530 2009
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 AlteredExpression group LHGDN A tissue microarray containing 86 specimens from esophageal cancer and 40 specimens from adjacent non-cancer tissue was constructed to survey the expression of p53, p16 and COX-2 by immunohistochemistry. 17650224 2007
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 AlteredExpression group BEFREE A tissue microarray containing 86 specimens from esophageal cancer and 40 specimens from adjacent non-cancer tissue was constructed to survey the expression of p53, p16 and COX-2 by immunohistochemistry. 17650224 2007
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 AlteredExpression group BEFREE However, down-regulation of p16 and p21 occurred frequently in esophageal cancer, owing to aberrant gene promoter methylation. 16488074 2007
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 PosttranslationalModification group LHGDN Inactivation of p16, RUNX3, and HPP1 occurs early in Barrett's-associated neoplastic progression and predicts progression risk. 15824739 2005
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 PosttranslationalModification group BEFREE Treatment of human esophageal cancer KYSE 510 cells with 5-50 microM of EGCG for 12-144 h caused a concentration- and time-dependent reversal of hypermethylation of p16(INK4a), retinoic acid receptor beta (RARbeta), O(6)-methylguanine methyltransferase (MGMT), and human mutL homologue 1 (hMLH1) genes as determined by the appearance of the unmethylation-specific bands in PCR. 14633667 2003
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group RGD These data, obtained using a unique in vivo model for esophageal cancer with rapid tumor induction, provide strong evidence for a link between deregulation of the p16ink4a-cyclin D1/Cdk4-Rb pathway and the initiation of esophageal tumors. 10969811 2000
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 AlteredExpression group BEFREE The dual hits (concomitant loss) of pRb and p16INK4a expression suggest that these two components are not mutually exclusive, and can both be altered in a significant proportion of primary ESCCs serving as putative diagnostic markers for esophageal cancer. 11079730 2000
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 PosttranslationalModification group BEFREE Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China. 9934853 1999
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 GeneticVariation group BEFREE p53 and p16/CDKN2 gene mutations in esophageal tumors from a high-incidence area in South Africa. 9808520 1998
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE We report a highly frequent homozygous deletion of the p16/CDKN2 gene in the esophageal cancer cell line and a relatively high frequency of homozygous deletion in gastric cancer cell lines. 7614482 1995
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 GeneticVariation group BEFREE These findings suggest that loss or mutations of the p16 gene are involved in most esophageal cancers and that mutation of this gene plays a critical role in the development of esophageal cancer. 8093026 1994
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 Biomarker group BEFREE Esophageal cancer is one primary human tumor in which MTS1 constitutes an apparent target of heterozygous or homozygous deletions occurring at chromosome 9p21. 7970734 1994
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 GeneticVariation group UNIPROT