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MYC and lymphoma are reported together in 3 articles.

Gene

MYC

HGNC
HGNC:7553
31articles
31mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype

Lymphoma

428articles
428mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

3 records shown · first 60

Molecular complexity of diffuse large B-cell lymphoma: a molecular perspective and therapeutic implications.

PMID 38001281 | DOI 10.1007/s13353-023-00804-5 · Journal of applied genetics · 2024 · 4 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMYC“Genetic investigations, led by high-throughput sequencing, have unveiled recurrent mutations in genes such as MYC, BCL2, and BCL6, casting light on the underlying genetic chaos propelling DLBCL's aggressiveness.”0.98hgnc_dict_v1
phenotypelymphoma“Molecular complexity of diffuse large B-cell lymphoma: a molecular perspective and therapeutic implications.”0.98phenotype_alias_lexicon_v2
geneBCL2“Genetic investigations, led by high-throughput sequencing, have unveiled recurrent mutations in genes such as MYC, BCL2, and BCL6, casting light on the underlying genetic chaos propelling DLBCL's aggressiveness.”0.98hgnc_dict_v1
geneBCL6“Genetic investigations, led by high-throughput sequencing, have unveiled recurrent mutations in genes such as MYC, BCL2, and BCL6, casting light on the underlying genetic chaos propelling DLBCL's aggressiveness.”0.98hgnc_dict_v1

Gut-derived Endotoxin-TLR4 Signaling Drives MYC-Ig Translocation to Promote Lymphoproliferation through c-JUN and STAT3 Activation.

PMID 36287175 | PMCID PMC9898117 | DOI 10.1158/1541-7786.MCR-19-1209 · Molecular cancer research : MCR · 2023 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMYC“TLR4 activation in turn caused c-JUN-dependent and STAT3-dependent translocations of MYC loci to suppress transactivation of CD95/FAS.”0.98hgnc_dict_v1
phenotypelymphoma“UNLABELLED: Synergism between obesity and virus infection promotes the development of B-cell lymphoma.”0.98phenotype_alias_lexicon_v2
geneSTAT3“Gut-derived Endotoxin-TLR4 Signaling Drives MYC-Ig Translocation to Promote Lymphoproliferation through c-JUN and STAT3 Activation.”0.98hgnc_dict_v1
geneTLR4“TLR4 activation in turn caused c-JUN-dependent and STAT3-dependent translocations of MYC loci to suppress transactivation of CD95/FAS.”0.98hgnc_dict_v1

Dysregulation of miRNAs in DLBCL: Causative Factor for Pathogenesis, Diagnosis and Prognosis.

PMID 34679437 | PMCID PMC8535125 | DOI 10.3390/diagnostics11101739 · Diagnostics (Basel, Switzerland) · 2021 · 7 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMYC“Recently miRNAs were also identified to act either as oncogenes or tumor suppressors in DLBCL pathology by altering the expression levels of some of the known DLBCL related oncogenes. i.e., miR-155, miR-17-92 and miR-21 act as oncogenes by altering the expression levels of MYC, SHIP and FOXO1, respectively, conversely; miR-34a, mir-144 and miR-181a act as tumor suppressors by altering the expression levels of SIRT1, BCL6 and CARD11, respectively.”0.98hgnc_dict_v1
phenotypelymphoma“Diffuse large B-cell lymphoma (DLBCL) is an aggressive non-Hodgkin's lymphoma (NHL), arising from different stages of B-cell differentiation whose pathogenesis involves miRNAs.”0.98phenotype_alias_lexicon_v2
geneBCL6“These genetic mutations are involved in epigenetic modification, ability to escape immunosurveillance, impaired BCL6 and NF-κβ signaling pathways and blocking terminal differentiation.”0.98hgnc_dict_v1
geneFOXO1“Recently miRNAs were also identified to act either as oncogenes or tumor suppressors in DLBCL pathology by altering the expression levels of some of the known DLBCL related oncogenes. i.e., miR-155, miR-17-92 and miR-21 act as oncogenes by altering the expression levels of MYC, SHIP and FOXO1, respectively, conversely; miR-34a, mir-144 and miR-181a act as tumor suppressors by altering the expression levels of SIRT1, BCL6 and CARD11, respectively.”0.98hgnc_dict_v1