Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 GeneticVariation disease BEFREE Expression of Kirsten rat sarcoma viral oncogene [Kras(G12V)] and disruption of cyclin-dependent kinase inhibitor 2A (CDKN2A; p16p19) in prospectively isolated satellite cells gave rise to pleomorphic rhabdomyosarcomas (MyoD-, Myogenin- and Desmin-positive), whereas introduction of the same oncogenetic hits in nonmyogenic progenitors induced pleomorphic sarcomas lacking myogenic features. 22135462 2011
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 Biomarker disease RGD Methylation of RAR-β2, RASSF1A, and CDKN2A genes induced by nickel subsulfide and nickel-carcinogenesis in rats. 21565688 2011
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 Biomarker disease BEFREE We previously showed that PAX3-FKHR expression in primary human myoblasts, cells that can give rise to RMS, cooperated with loss of p16INK4A to promote extended proliferation. 19047133 2008
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 Biomarker disease BEFREE No mutations were detected in exons 14-21 of MET whereas a nonsense mutation at codon 80 of p16(INK4A) was identified in an alveolar RMS cell line. 17243166 2007
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 Biomarker disease LHGDN The PAX3-FKHR fusion gene of rhabdomyosarcoma cooperates with loss of p16INK4A to promote bypass of cellular senescence. 17638879 2007
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 GeneticVariation disease BEFREE Expression of the p16INK4A (p16), p15INK4B (p15), and p14ARF genes, located at 9p21, was examined in pediatric neuroblastoma (NB), Ewing's sarcoma (ES), and rhabdomyosarcoma (RMS). p16 expression was absent in 4 of 5 ESs, and 2 of these 4 cases died. p16 expression was reduced or absent in 10 of 12 RMSs, and 4 of these 10 cases died. 12963998 2003
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 Biomarker disease LHGDN The marked synergism in mice between aberrant c-Met signaling and Ink4a/Arf inactivation, lesions individually implicated in human RMS, suggests a therapeutic combination to combat this devastating childhood cancer. 12368906 2002
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 Biomarker disease BEFREE Our data indicate that human c-MET and INK4a/ARF, situated at the nexus of pathways regulating myogenic growth and differentiation, represent critical targets in RMS pathogenesis. 12368906 2002
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 GeneticVariation disease BEFREE To confirm the significance of p16 gene deletion in tumour biology of RMS, a temperature-sensitive p16 mutant (E119G) gene was retrovirally transfected into the human RMS cell line RD, which has homozygous gene deletion of p16 gene. 10098732 1999
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 GeneticVariation disease BEFREE PCR-SSCP analysis of exons 1 and 2 of CDKN2A gene revealed only one missense mutation in codon 15 in a rhabdomyosarcoma. 9664128 1998
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.290 GeneticVariation disease BEFREE We looked for homozygous deletions of CDKN2A, CDKN2B (p15INK4B), and CDKN2C (p18) in 12 primary rhabdomyosarcoma (RMS) specimens and in five cell lines established from this cancer type. 8703847 1996