H3P10, H3 histone pseudogene 10, 115482713

N. diseases: 769; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We sought to determine whether p15 is a useful immunohistochemical marker to distinguish Spitz nevi from spitzoid melanomas and to compare p15 and p16 staining in this population. 30666677 2019
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Methylation frequency of CLDN11 (OR, 25.56; 95% CI, 2.32-281.66; p = 0.008), MGMT (OR, 4.64; 95% CI, 1.98-10.90; p = 0.0004), p16 (OR, 4.31; 95% CI, 1.33-13.96; p = 0.01), and RASSF1A (OR, 10.10; 95% CI, 2.87-35.54; p = 0.0003) was significantly higher in metastasis melanoma compared with controls. 30370527 2019
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE We found statistically significant differences between Spitz nevus and melanoma for the following features: pagetoid spread, atypia, maturation, elastosis, Kamino bodies, p16 expression, and the staining pattern of HMB45. 29417221 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE The combination of highly atypical cytomorphology and architecture, increased mitoses, and p16 expression loss compelled the diagnosis of melanoma. 29771690 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Immunohistochemistry for p16 has been recently utilized to distinguish benign nevi from melanoma. 30178478 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Melanocyte proliferation is activated by <i>BRAF</i><sup>V600E</sup>, then is arrested, but single nevi transform to melanomas. p16 controls arrest, and p16 loss may promote transformation. 29507566 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE There was not a significant difference between p16 staining in benign blue nevi and melanoma (P=0.06). 26766120 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We have performed a gain-of-function screen of 17,030 lentivirally expressed human open reading frames (ORFs) in a melanoma cell line containing an inducible p16 construct to identify such genes. 27872202 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE By H score, p16 expression was significantly higher in Spitz nevi relative to ASTs or spitzoid melanomas. 27569296 2016
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Melanomas expressing p16 had a slower growth rate than melanomas without p16 expression (2·27 vs. 4·34 mm(2) /year, P = 0·047). 26613644 2016
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Although decreased p16 expression has been associated with melanoma formation, in recent work, p15 represented a primary effector of oncogene-induced senescence in nevomelanocytes that was diminished in melanomas. 27855847 2016
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE Participants in all groups continued to rate photoprotection as highly effective in reducing melanoma risk and reported decreased beliefs that carrying the p16 mutation would inevitably lead to the development of melanoma. 25822116 2015
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Expression of p16 and mutated BRAF proteins was also evaluated in 17 conventional (nonspitzoid) melanomas with homozygous 9p21 loss and the 2 groups of ASTs. 24451276 2014
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE We compared the gene expression profile of SFs from FM individuals with two distinct CDKN2A/p16 mutations (V126D-p16 and R87P-p16) with the gene expression profile of SFs from age-matched individuals without p16 mutations and with no family history of melanoma. 23371019 2013
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE This study demonstrates the biological connection between the known melanoma genes p16 (CDKN2A) and BRAF in a normal physiological response to UVR in the skin, and highlights the importance of defects in this biological pathway to melanoma and squamous cell carcinoma development. 21923753 2012
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Statistical analysis was used to compare p16 expression, mitotic count/mm(2), and Ki-67 index of childhood nodular malignant melanomas and Spitz nevi. 21550132 2011
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Higher expression of p16 and Ptch in melanoma and BCC of the skin was frequently detected in studied cases. 19287961 2009
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE We conclude that HNSCC in young individuals should prompt clinicians to obtain a family history and consider that the patient may have a germline p16 defect that could predispose them to other cancers, including melanoma and pancreatic cancer. 19360740 2009
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE The combination of MMR gene mutations and abnormalities of p16 or other molecular pathways is needed to induce melanocytic carcinogenesis in a familial setting as well as in sporadic MM. 18460031 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 PosttranslationalModification disease BEFREE Genetic and epigenetic analyses of the human 9p21 locus indicate that modifications of ARF occur independently of p16 inactivation in human melanoma and suggest that ARF is more frequently inactivated than p16. 18505964 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE Our data suggest that the P48T mutation of p16 is a strong melanoma-predisposing factor, but the fact that the heterozygous mutant parents have not yet exhibited melanoma or atypical moles indicates that the penetrance of this allele might depend on modifying factors. 17625456 2007
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE To date several studies indicate the effective implication of p16 as a tumor suppressor gene with a major role in either the development or progression of human melanoma. 17218782 2007
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE GenoMEL, comprising major familial melanoma research groups from North America, Europe, Asia, and Australia has created the largest familial melanoma sample yet available to characterize mutations in the high-risk melanoma susceptibility genes CDKN2A/alternate reading frames (ARF), which encodes p16 and p14ARF, and CDK4 and to evaluate their relationship with pancreatic cancer (PC), neural system tumors (NST), and uveal melanoma (UM). 17047042 2006
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE In this model, conversion from a senescent nevus to a malignant melanoma is accompanied by loss of expression of p16. 16917802 2006
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE The level of p16 expression gradually decreased from benign nevi to melanoma without metastasis to melanoma with metastasis. 16331607 2006