Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 AlteredExpression disease BEFREE EZH2 overexpression in primary gastrointestinal diffuse large B-cell lymphoma and its association with the clinicopathological features. 28438623 2017
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 GeneticVariation disease BEFREE Prioritized alterations in epigenetic modulators were common and included gain-of-function EZH2 and loss-of-function ARID1A mutations (14% of diffuse large B-cell lymphomas and 22% of follicular lymphomas contained alterations in each of these two genes). 27102345 2016
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 Biomarker disease CTD_human These mutations, which result in the replacement of a single tyrosine in the SET domain of the EZH2 protein (Tyr641), occur in 21.7% of GCB DLBCLs and 7.2% of FLs and are absent from ABC DLBCLs. 20081860 2010
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 AlteredExpression disease BEFREE Degradation of PRC2 with UNC6852 blocks the histone methyltransferase activity of EZH2, decreasing H3K27me3 levels in HeLa cells and diffuse large B cell lymphoma (DLBCL) cells containing EZH2 gain-of-function mutations. 31831267 2020
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 GeneticVariation disease BEFREE Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin. 20081860 2010
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 AlteredExpression disease BEFREE We investigated RUNX3 and EZH2 expression in diffuse large B-cell lymphoma (DLBCL). 27184221 2017
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 AlteredExpression disease BEFREE Tazemetostat, first-in-class EZH2 inhibitor, demonstrated enhanced clinical activity in mutant follicular lymphoma and diffuse large B cell lymphoma. 30112706 2018
Entrez Id: 2146
Gene Symbol: EZH2
EZH2
0.700 GeneticVariation disease BEFREE In particular, recurrent gain-of-function mutations targeting EZH2 Y641 occur most frequently in follicular lymphoma and aggressive diffuse large B-cell lymphoma and are associated with H3K27me3 hyperactivation, which contributes to lymphoma pathogenesis. 24469040 2015
Entrez Id: 5293
Gene Symbol: PIK3CD
PIK3CD
0.600 Biomarker disease BEFREE Furthermore, CUDC-907, a small-molecule dual-acting inhibitor of both class I and II HDACs and class I PI3Ks, effectively suppresses the growth and survival of MYC-altered or MYC-dependent cancer cells, such as DH DLBCL and BRD-NUT fusion-positive NUT midline carcinoma (NMC) cells, and MYC protein downregulation is an early event induced by CUDC-907 treatment. 27980108 2017
Entrez Id: 4615
Gene Symbol: MYD88
MYD88
0.600 GeneticVariation disease BEFREE Testicular, breast, and uterine DLBCL (as well as possibly primary cutaneous DLBCL, leg-type) share a high prevalence of the non-germinal center B cell (non-GCB) phenotype and the MYD88/CD79B-mutated (MCD) genotype. 29931605 2018
Entrez Id: 974
Gene Symbol: CD79B
CD79B
0.600 Biomarker disease CTD_human Here we report that constitutive activity of PI3K and the downstream kinase PDK1 are essential for the viability of two ABC DLBCL cell lines that carry mutations in the BCR proximal signaling adaptor CD79B. 21173233 2011
Entrez Id: 4615
Gene Symbol: MYD88
MYD88
0.600 AlteredExpression disease BEFREE In univariate analysis, MYD88 overexpression was correlated with shortened disease-free survival (DFS) of DLBCL (P = .013) and non-germinal center B-cell-like DLBCL (P = .034). 23380077 2013
Entrez Id: 4615
Gene Symbol: MYD88
MYD88
0.600 Biomarker disease BEFREE When compared with normal lymph nodes, the MYD88 is significantly amplified in primary testicular DLBCL. 26388135 2015
Entrez Id: 4615
Gene Symbol: MYD88
MYD88
0.600 GeneticVariation disease BEFREE The recurrent MyD88 L265P mutation, present in 29% of ABC DLBCL, was reported as an independent poor prognostic factor for patients with newly diagnosed DLBCL. 28847710 2017
Entrez Id: 974
Gene Symbol: CD79B
CD79B
0.600 CausalMutation disease CGI
Entrez Id: 5293
Gene Symbol: PIK3CD
PIK3CD
0.600 Biomarker disease BEFREE In this study, expression of the important components of the phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) signaling pathway and their clinical significance were investigated in 73 DLBCL cases. 23636313 2013
Entrez Id: 5293
Gene Symbol: PIK3CD
PIK3CD
0.600 AlteredExpression disease BEFREE In the present study, we demonstrated that PF-04691502, a novel PI3K/mTOR inhibitor has potent activity in a panel of aggressive B-NHL cell lines including diffuse large B-cell lymphoma (DLBCL) and mantle cell lymphoma (MCL). 26549638 2016
Entrez Id: 974
Gene Symbol: CD79B
CD79B
0.600 GeneticVariation disease BEFREE Patients with primary breast and primary female genital tract diffuse large B cell lymphoma have a high frequency of MYD88 and CD79B mutations. 28803429 2017
Entrez Id: 4615
Gene Symbol: MYD88
MYD88
0.600 GeneticVariation disease BEFREE Also, MYD88 L265P had little involvement in GI DLBCL compared with other extranodal DLBCLs, suggesting that its pathogenesis might be different from that of organs with a high frequency of MYD88 L265P. 27439595 2016
Entrez Id: 4615
Gene Symbol: MYD88
MYD88
0.600 Biomarker disease CTD_human Blockade of oncogenic IκB kinase activity in diffuse large B-cell lymphoma by bromodomain and extraterminal domain protein inhibitors. 25049379 2014
Entrez Id: 84433
Gene Symbol: CARD11
CARD11
0.600 CausalMutation disease CGI
Entrez Id: 974
Gene Symbol: CD79B
CD79B
0.600 GeneticVariation disease BEFREE In a number of B-cell malignancies, activating mutations in signal transduction components of the BCR pathway have been identified; prominent examples are activated B-cell-like (ABC) diffuse large B-cell lymphomas (DLBCL) that carry mutations in CD79B and CARD11 and display chronic active BCR signaling resulting in constitutive activation of the NF-κB pathway. 24060900 2013
Entrez Id: 84433
Gene Symbol: CARD11
CARD11
0.600 Biomarker disease BEFREE We conclude that mutations of the oncogene CARD11 may contribute to NF-kappaB activation and thereby play a role in the pathogenesis of PCNSL, while, in contrast to systemic DLBCL, inactivation of TNFAIP3 either by mutation or methylation seems to be of minor significance. 20544211 2010
Entrez Id: 84433
Gene Symbol: CARD11
CARD11
0.600 AlteredExpression disease BEFREE To this end, we expressed oncogenic CARMA1 in the NF-κB negative DLBCL lymphoma cell line BJAB. 26776161 2016
Entrez Id: 974
Gene Symbol: CD79B
CD79B
0.600 GeneticVariation disease BEFREE Morphologic Patterns and the Correlation With MYD88 L265P, CD79B Mutations in Primary Adrenal Diffuse Large B-Cell Lymphoma. 31609782 2020