TP53, tumor protein p53, 7157

N. diseases: 2494; N. variants: 527
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE TP53 alteration in primary tumour was significantly associated with the following parameters: positive node status, T status > 1, negative oestrogen receptor status, negative progesterone receptor status, presence of ERBB2 gene amplification, and invasive ductal histology. 8102535 1993
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Of note, human genomic databases (TCGA, METABRIC etc.) show a high degree of p53 LOH in all examined tumor types that carry missense p53 mutations, including sarcomas and breast carcinomas (with and without HER2 amplification). 28277540 2017
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE HER-2 gene amplification and TP53 gene deletion were detected in CTCs. 21527564 2011
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE We found elevated risks of disease recurrence and overall mortality in patients with both p53 mutation and neu/erbB-2 amplification in their tumor compared with patients with neither or only one of the alterations. 14701769 2004
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE HER-2/neu amplification was identified in 12 of 30 DCIS samples (40%), and p53 mutations were identified in 6 of 30 DCIS samples (20%). 11147584 2000
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE All cases showing p53 mutations or HER-2 amplification represented protein expression of p53 or HER-2, respectively. 9338750 1997
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Patients carrying a TP53 mutation showed a significantly higher likelihood of developing a breast cancer with Human Epidermal growth factor Receptor (HER2) amplification (83%) when compared to the cohort of young onset breast cancer cases (16%); ER and PR status were equivalent between groups. 20805372 2010
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Heterogeneous gene alterations in primary breast cancer contribute to discordance between primary and asynchronous metastatic/recurrent sites: HER2 gene amplification and p53 mutation. 12738987 2003
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE There was a significant association between HER-2/neu amplification and deletion of a p53 allele. 24399009 2013
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Patients with TP53 mutation (-) PIK3CA mutation (-) ERBB2 amplification (+) CCND1 amplification (-), TP53 mutation (+) PIK3CA mutation (-) ERBB2 amplification (+) CCND1 amplification (-) or TP53 mutation (+) PIK3CA mutation (+) ERBB2 amplification (+) CCND1 amplification (-)had significantly higher pCR rates (P < 0.05 for ypT0/isypN0 and ypT0/is) than wild type genotype tumors. 30776175 2019
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Our analysis showed that GAED frequently harbors TP53 mutations and ERBB2 amplification. 29751042 2018
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Together, resistance to HER2 blockade should be indicated during treatment if any of the following situations applies: 1) recurrence or persistence of HER2 amplification in the blood; 2) emergence or ≥20% increase in the fraction of mutations in any of these resistance-related genes including TP53/PIK3CA/MTOR/PTEN. 27602761 2016
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE TP53 mutational status (exons 2-10) and ERBB2 amplification status were determined in tumor specimens from a prospective cohort of 543 women with node-negative breast cancer. 17221157 2007
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE No such correlation is found for p53 mutations or erbB2 amplification. 1306132 1992
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE Since p53 mutations as well as c-erbB-2 amplification were detected almost selectively in Grade 3 cases but were not associated with lymph nodal status in invasive breast cancer, these two gene alterations could be indicators of prognosis of disease independent of lymph nodal status. 8099903 1993
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE TP53 mutations and ERBB2 amplification were more frequent in SDCXPA than in SDCDN (P = .0007 and P = .01, respectively). 30946933 2019
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE TP53 mutations (15/27, 56%), PTEN loss (11/29, 38%, including 2 cases with PTEN mutation), PIK3CA hotspot mutations (10/30, 33%), HRAS hotspot mutations (10/29; 34%), and ERBB2 amplification (9/29, 31%, including 1 case with mutation) represented the 5 most common abnormalities. 25723113 2015
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 GeneticVariation disease BEFREE In patients with CCNE1 amplification (n = 28), TP53 mutations (n = 23, 82.1%) and ERBB2 amplification (n = 8, 28.6%) were the most frequent concurrent genetic alterations. 31178228 2019
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE By conventional light microscopy, HER-2/neu amplification (>/=6 copies >50% cancer cells) was detected in 14% (8/59) tumours, HER-2/neu overexpression (>10% cells moderate/strong complete membrane staining) in 22% (13/60) for A0485, and 18% (11/60) for TAB250, p53 (>10% +cells) in 61% (36/59), and Ki-67 (>50% +cells) in 50% (30/60). 14752523 2004
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE While TOP2alpha and p53 gene amplification was detected in no case, 5 cases (8%) showed HER2 gene amplification, which was related to HER2 3+ score in 4 cases. 15816547 2005
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE Additional FISH studies that use probes to the SMS, RARA, and TP53 genes are an effective way to determine the true HER2 amplification status in patients with polysomy 17 and they have important potential implications for guiding HER2-targeted therapy in breast cancer. 21947821 2011
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE In addition, a Fluorescent In Situ Hybridization (FISH) assay for HER2 gene amplification and p53 genotyping was performed on all cell lines. 23372829 2013
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE The association between TP53 mutation and ERBB2 amplification was confirmed in a wider DCIS cohort using p53 immunohistochemistry as a surrogate marker for TP53 mutations (P=0.03). 28338653 2017
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE FISH analysis showed erbB-2 gene amplification and p53 deletions in selected CIS, as well as a marked chromosome 17 copy number heterogeneity in all six CIS examined. 7672797 1995
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.100 Biomarker disease BEFREE In this study, we now show that p53 positivity in unamplified 17 polysomy identifies cases that are associated with an even higher Nottingham score and greater hormone receptor negativity that is similar to cases with HER2 amplification. 20823770 2011