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Genes (21)
Species: human : 21 | |
Human | PRAME | 23532 | preferentially expressed antigen in melanoma | Overexpression of PRAME was associated with childhood acute leukemia | Human | MVP | 9961 | major vault protein | Relationship between major vault protein/lung resistance protein, multidrug resistance-associated protein, P-glycoprotein expression, and drug resistance in childhood leukemia. BACKGROUND : Previous studies revealed that lung resistance protein (LRP) and multidrug resistance-associated protein (MRP) relate to drug resistance of childhood leukemia, which is not caused by only one mechanism. | Human | AKR1C3 | 8644 | aldo-keto reductase family 1, member C3 | The maternal methylenetetrahydrofolate reductase A1298C polymorphism was found to be an effect modifier of the maternal intron 4 polymorphism of the AKR1C3 gene and the childhood leukemia risk | Human | WT1 | 7490 | Wilms tumor 1 | High levels of WT1 expression is associated with childhood acute leukemia | Human | TPMT | 7172 | thiopurine S-methyltransferase | These results indicate that polymerase chain reaction-based assays give reliable and robust results for the detection of TPMT deficiency, but that caution should be exercised in relying exclusively on DNA obtained from lymphoblasts in childhood leukaemia. This study examined the role of thiopurine methyltransferase (TPMT) polymorphism in the metabolism and clinical effects of azathioprine and 6-mercaptopurine in the treatment of inflammatory bowel disease and childhood leukemia. | Human | TP53 | 7157 | tumor protein p53 | higher expression in childhood leukemias with poor prognosis compared to long-term survivors | Human | TCF3 | 6929 | transcription factor 3 | Our observations suggest that there could be heterogeneity in the molecular events among adult leukemias carrying the t(1;19) and that the E2A/PBX1 fusion formation might also be associated with an adverse treatment outcome in adult leukemias as in childhood leukemias. Identification of a novel molecular partner of the E2A gene in childhood leukemia. | Human | PTPN11 | 5781 | protein tyrosine phosphatase, non-receptor type 11 | Recent identification of SHP-2 mutations in childhood leukemia further emphasizes the importance of SHP-2 regulation in hematopoietic cells. | Human | PBX1 | 5087 | pre-B-cell leukemia homeobox 1 | Our observations suggest that there could be heterogeneity in the molecular events among adult leukemias carrying the t(1;19) and that the E2A/PBX1 fusion formation might also be associated with an adverse treatment outcome in adult leukemias as in childhood leukemias. | Human | NBN | 4683 | nibrin | The TT genotype of c.2071-30A>T polymorphism was higher in leukaemia patients than in controls. results suggest that some specific haplotypes of the NBS1 gene may be associated with childhood leukaemia | Human | MTRR | 4552 | 5-methyltetrahydrofolate-homocysteine methyltransferase reductase | polymorphic variants of genes GSTT1, GSTM1, NAT2 and MTRR can modulate the risk of childhood acute leukemia, residents of European part of Russia | Human | MTHFR | 4524 | methylenetetrahydrofolate reductase (NAD(P)H) | The maternal methylenetetrahydrofolate reductase A1298C polymorphism was found to be an effect modifier of the maternal intron 4 polymorphism of the aldo-keto reductase family 1 member C3 gene and the childhood leukemia risk | Human | MLLT4 | 4301 | myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4 | AF6 is a recurrent fusion partner of MLL, the human homolog of Drosophila trithorax chromatin remodeling protein that is involved in childhood leukemia and mixed lineage leukemia. | Human | MDM2 | 4193 | MDM2 oncogene, E3 ubiquitin protein ligase | higher expression in childhood leukemias with poor prognosis compared to long-term survivors | Human | IGFBP3 | 3486 | insulin-like growth factor binding protein 3 | OBJECTIVE: To investigate whether the three principal components of the insulin-like growth factor (IGF) system, IGF-1, IGF-2 and IGF binding protein-3 (IGFBP-3), are associated with survival from childhood leukemia. Because IGFBP-3 is essentially a binding protein, we interpret our findings as indicating that bioavailable IGF-I may play an important role in the aetiology of childhood leukaemia. Since insulin-like growth factor-I (IGF-I) mediates the effect of growth hormone and has been positively associated with prostate cancer, we have evaluated the role of this hormone and its principal binding protein, IGFBP-3, in the aetiology of childhood leukaemia. Insulin-like growth factor binding protein-3 predicts survival from acute childhood leukemia. OBJECTIVE: Insulin-like growth factor-1 (IGF-1) and its principal binding protein-3 (IGFBP-3) are central in the mediation of the effect of growth hormone, and the IGF system has been reported to play a role in the pathogenesis of childhood leukemia. CONCLUSION: The presented empirical evidence in conjunction with the fact that IGFBP-3 modulates IGF-1 and IGF-2 bioavailability and is likely to have proapoptotic effects makes this compound a plausible independent predictor of survival from childhood leukemia. There was no significant association between IGF-I and the likelihood of childhood leukaemia, but an increment of 1 microg/ml of IGFBP-3 was associated with a substantial and statistically significant reduction of childhood leukaemia by 28% (95% confidence interval 7% to 45%). | Human | HFE | 3077 | hemochromatosis | Title:The C282Y mutation of HFE is another male-specific risk factor for childhood acute lymphoblastic leukemia|Association:Y|Conclusion: | Human | ERCC1 | 2067 | excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence) | This is the first report describing a mutation at the ERCC1 gene in acute childhood leukaemia. | Human | NQO1 | 1728 | NAD(P)H dehydrogenase, quinone 1 | This is the first study showing robust (to bias due to population structure) evidence that the NQO1 C609T variant is a risk factor for childhood leukemia | Human | CYP1A1 | 1543 | cytochrome P450, family 1, subfamily A, polypeptide 1 | The risk of childhood leukemia showed no evidence of association between cytochrome P-450 1A1 genotype frequencys and case control status | Human | CDKN1B | 1027 | cyclin-dependent kinase inhibitor 1B (p27, Kip1) | Mutations in the 3' untranslated region of Kip1 could provide an additional tool for risk classification in childhood leukemia | Human | RUNX1 | 861 | runt-related transcription factor 1 | Amplification of this gene in childhood acute lymphoblsatic leukemia is associatd with poor outcome |
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