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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 60Molecular 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
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYC | “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.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “Molecular complexity of diffuse large B-cell lymphoma: a molecular perspective and therapeutic implications.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | BCL2 | “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.” | 0.98 | hgnc_dict_v1 |
| gene | BCL6 | “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.” | 0.98 | hgnc_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
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYC | “TLR4 activation in turn caused c-JUN-dependent and STAT3-dependent translocations of MYC loci to suppress transactivation of CD95/FAS.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “UNLABELLED: Synergism between obesity and virus infection promotes the development of B-cell lymphoma.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | STAT3 | “Gut-derived Endotoxin-TLR4 Signaling Drives MYC-Ig Translocation to Promote Lymphoproliferation through c-JUN and STAT3 Activation.” | 0.98 | hgnc_dict_v1 |
| gene | TLR4 | “TLR4 activation in turn caused c-JUN-dependent and STAT3-dependent translocations of MYC loci to suppress transactivation of CD95/FAS.” | 0.98 | hgnc_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
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYC | “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.” | 0.98 | hgnc_dict_v1 |
| phenotype | lymphoma | “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.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | BCL6 | “These genetic mutations are involved in epigenetic modification, ability to escape immunosurveillance, impaired BCL6 and NF-κβ signaling pathways and blocking terminal differentiation.” | 0.98 | hgnc_dict_v1 |
| gene | FOXO1 | “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.” | 0.98 | hgnc_dict_v1 |