CTNNB1, catenin beta 1, 1499

N. diseases: 1368; N. variants: 68
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE Increased cytoplasmic and/or nuclear beta-catenin staining was seen in 94% and 80% of the adenomas. beta-Catenin nuclear staining was strongly associated with MYC levels (p value 0.03) but not with KRAS mutations.Copy number aberrations were rare. 20196079 2010
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE In conclusion, the molecular and pathological classification of hepatocellular adenomas permits the identification of strong genotype-phenotype correlations and suggests that adenomas with beta-catenin activation have a higher risk of malignant transformation. 16496320 2006
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE No mutations or deletions were seen in exon 3 of the beta-catenin gene for either the adenomas or the carcinoma. 18246041 2008
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE Consistent with the presence of WNT pathway gene alterations, all superficially serrated adenomas showed focal or diffuse nuclear β-catenin accumulation. 29789649 2018
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE In non-ampullary lesions, abnormal nuclear localization of β-catenin was observed in 21 (84.0%) of 25 adenomas and 4 (33.3%) of 12 adenocarcinomas. 28467793 2017
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE Furthermore, aberrant β-catenin staining co-localized with DR4 and DR5 expression in 92% of adenomas. 24379239 2014
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE In mice with heterozygous disruption of Apc(APC(Δ1638/+)), Smad4-deficient intestinal adenomas had increased levels of β-catenin mRNA and expression of Wnt target genes compared with adenomas from APC(Δ1638/+) mice that expressed Smad4. 22115830 2012
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE The clinical, pathological, and immunophenotypic (hMLH1, hMSH2, MGMT, MIB-1, p53, and beta-catenin) properties of 28 mixed hyperplastic and adenomatous polyps of the colon (7 of which also contained carcinoma within the same lesion) were evaluated for the above immunopeptides in each of the different morphologic areas of the polyps, and the results were compared to traditional hyperplastic polyps, serrated adenomas, and conventional (nonserrated) adenomas. 15712188 2005
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE Adenomas and carcinomas showing both nuclear and reduced membranous expression of beta-catenin, compared with those with normal membranous expression, tended to show allele loss ( P<0.01). 11956815 2002
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE In the context of APC (adenomatous polyposis coli) deficiency (Apc(Min/+) mice), loss of Fbxw7 accelerated intestinal tumorigenesis and death and promoted accumulation of β-catenin in adenomas at late but not early time points. 21282377 2011
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE Similar to sporadic CRC, CTNNB1 was frequently activated at the adenoma stage, and TP53 mutation occurred during cancer development from adenoma. 27563825 2016
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE It occurred at the transition to dysplasia in serrated polyps with a significant increase in nuclear β-catenin labeling from sessile serrated adenomas (10%) to sessile serrated adenomas with dysplasia (55%) and traditional serrated adenomas (9%) to traditional serrated adenomas with dysplasia (39%) (P=0.0001). 29148535 2018
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE We report a case of a well-differentiated hepatocellular neoplasm with Dubin-Johnson-like pigment displaying histological features overlapping with a beta-catenin mutated inflammatory adenoma and a well-differentiated hepatocellular carcinoma in a non-cirrhotic liver. 26663015 2015
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE β-Catenin stained the cell membrane, cytoplasm, and nuclei of the adenoma. 25449630 2015
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE Four APAs showed a predominant (≥50%) zona fasciculata-like cell pattern: one tumor had CYP11B1 H-score = 150, no detectable CYP11B2 expression, and harbored a PRKACA p.Leu206Arg mutation (that we have reported previously elsewhere), one had no CYP11B1 expression, CYP11B2 H-score = 40, and no mutations; the remaining two adenomas had high CYP11B1 H-score (160 and 240, respectively) and low CYP11B2 H-score (30 and 15, respectively), with the latter harboring a CTNNB1 p.Ser45Phe activating mutation. 28405879 2017
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE Immunohistochemical analysis of adenomas revealed increased nuclear beta-catenin accumulation in adenomas from Rassf1a(-/-); Apc(+/Min) mice, compared to those from Rassf1a(+/+); Apc(+/Min) mice, but no differences in proliferation marker (Ki67) staining patterns. 18391979 2008
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE Sequencing analyses identified APC or CTNNB1 mutations in the majority of sporadic adenomas (58/84, 69%) and MMR-proficient Lynch syndrome-associated adenomas (13/18, 72%). 28548127 2017
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE Expression profiling revealed that ISC signatures, as well as the Wnt/β-catenin and Notch signaling pathways are downregulated in Ap4-deficient adenomas and intestinal organoids. 30177706 2018
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE The lower apoptotic activity of low-grade slightly elevated adenomas can be partly attributed to upregulated β-catenin pathway activity and downregulated c-Myc expression. 28533663 2017
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE Somatic mutations of β-catenin and PRKACA are observed in non secreting or cortisol producing adenomas, respectively. 26038203 2015
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE Here, we focused our investigation on the beta-catenin gene which is implicated in colorectal carcinogenesis and tested whether beta-catenin mRNA is detectable in the plasma of colorectal carcinoma and adenoma patients using quantitative reverse transcriptase-PCR. 15014011 2004
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE We corroborated the Wnt/APC signalling pathway on the NT1 receptor promoter activation with human colon carcinogenesis, and showed that NT1 receptor gene activation was perfectly correlated with nuclear or cytoplasmic beta-catenin localization while NT1 receptor was absent when beta-catenin was localized at the cell-cell junction in early adenomas of patients with familial adenomatous polyposis, hereditary non-polyposis colorectal cancer and loss of heterozygosity tumours. 16299383 2006
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 Biomarker group BEFREE Analysis of K-ras, APC, and beta-catenin in aberrant crypt foci in sporadic adenoma, cancer, and familial adenomatous polyposis. 11522744 2001
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 GeneticVariation group BEFREE BRAF and beta-catenin mutations were detected in 3 and 8% of the 101 flat-type adenomas, respectively. 17143260 2007
CUI: C0001430
Disease: Adenoma
Adenoma
0.400 AlteredExpression group BEFREE Activation of β-catenin and ERK1/2 was mitigated in Apc(Min/+);Nherf2(-/-) adenomas. 26867566 2016