Hodgkin Disease
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Absence of Oct-2 and Bob-1 protein expression in primary H-RS cells was demonstrated by performing immunohistochemistry in 20 cases of classical Hodgkin's disease.
|
11280769 |
2001 |
Leukemia, Myelocytic, Acute
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Oct2 was expressed strongly in 12 of 16 AML cases with t(8;21) and 19 of 46 without t(8;21).
|
16891199 |
2006 |
Leukemia, Myelocytic, Acute
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Although OCT-2 and BOB.1 were not associated with PAX5 expression, we report expression of OCT-2 in AML with myelomonocytic/monocytic maturation and BOB.1 in normal hematopoietic elements.
|
17074681 |
2006 |
Leukemia, Myelocytic, Acute
|
0.040 |
Biomarker
|
disease |
BEFREE |
OCT-2 may act as a cell survival factor in AML by mediating expression of downstream targets, such as BCL-2.
|
20141429 |
2010 |
Leukemia, Myelocytic, Acute
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
To assess a large series of patients with acute myeloid leukemia (AML) with t(8;21) for both IGH@ and IGK@ B-cell gene rearrangements and for expression of PAX5, OCT2, and Bob.1 by immunohistochemistry and expression of CD19, CD79a, CD20, and CD22 by flow cytometry immunophenotyping.
|
23955454 |
2013 |
Classical Hodgkin's Lymphoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
It has previously been demonstrated that in cultured and in situ tumour cells of classical Hodgkin lymphoma (cHL), the immunoglobulin (Ig) promoter is inactive and its transcription factors Oct2 and/or BOB.1/OBF.1 are down-regulated.
|
14694522 |
2004 |
Classical Hodgkin's Lymphoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
All ptHL expressed CD15, CD30 and LMP-1 of EBV; the B-cell markers BOB-1, Oct2, CD79a and CD20 were more commonly expressed in ptHL versus cHL (100%, 86%, 50% and 38% in ptHL compared to 6%, 14%, 10% and 33% in cHL, respectively); all ptHL expressed phosphoinositide 3-kinase (PI3K) versus 81% of cHL; 2/6 (33%) ptHL displayed gains at 9p24 that were similar to cHL (32%).
|
19705967 |
2009 |
Classical Hodgkin's Lymphoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Ectopic expression of both Oct2 and PU.1 in a cHL cell line potentiated endogenous PU.1 and SYK expression after 5-aza-dC treatment.
|
16304050 |
2006 |
Classical Hodgkin's Lymphoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Immunohistochemical studies revealed that the large atypical cells were CD30 (+), CD15 (weakly +), CD20 (-), CD45 (-), Pax5 (weakly +), BOB.1 (-), and Oct2 (-), indicating the coexistence of SMZL with cHL.
|
18486899 |
2008 |
Adult Classical Hodgkin Lymphoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Immunohistochemical studies revealed that the large atypical cells were CD30 (+), CD15 (weakly +), CD20 (-), CD45 (-), Pax5 (weakly +), BOB.1 (-), and Oct2 (-), indicating the coexistence of SMZL with cHL.
|
18486899 |
2008 |
Adult Classical Hodgkin Lymphoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
It has previously been demonstrated that in cultured and in situ tumour cells of classical Hodgkin lymphoma (cHL), the immunoglobulin (Ig) promoter is inactive and its transcription factors Oct2 and/or BOB.1/OBF.1 are down-regulated.
|
14694522 |
2004 |
Adult Classical Hodgkin Lymphoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Ectopic expression of both Oct2 and PU.1 in a cHL cell line potentiated endogenous PU.1 and SYK expression after 5-aza-dC treatment.
|
16304050 |
2006 |
Adult Classical Hodgkin Lymphoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
All ptHL expressed CD15, CD30 and LMP-1 of EBV; the B-cell markers BOB-1, Oct2, CD79a and CD20 were more commonly expressed in ptHL versus cHL (100%, 86%, 50% and 38% in ptHL compared to 6%, 14%, 10% and 33% in cHL, respectively); all ptHL expressed phosphoinositide 3-kinase (PI3K) versus 81% of cHL; 2/6 (33%) ptHL displayed gains at 9p24 that were similar to cHL (32%).
|
19705967 |
2009 |
Renal Cell Carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
Previous studies have shown that loss of the human organic cation transporter OCT2 is the main factor contributing to oxaliplatin resistance in RCC, and that DNA hypermethylation and histone methylation play important roles in the transcriptional repression of <i>OCT2</i> in RCC.
|
31088315 |
2019 |
Renal Cell Carcinoma
|
0.030 |
PosttranslationalModification
|
disease |
BEFREE |
Epigenetic analysis revealed that the repressed OCT2 promoter in RCC is characterized by hypermethylated CpG islands and the absence of H3K4 methylation.
|
27440728 |
2016 |
Renal Cell Carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
Overall, this study indicated that miR-489-3p and miR-630 function as oncotherapy-obstructing microRNAs by directly targeting OCT2 in RCC.
|
31649850 |
2019 |
Diffuse Large B-Cell Lymphoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
The final diagnosis of EBV-positive DLBCL was confirmed based on the expression of B-cell-specific transcription factors (Oct-2 and BOB.1), PCR-based identification of monoclonal rearrangement of the immunoglobulin genes, and the presence of EBV-encoded small RNAs in the tumor cells (identified using in situ hybridization).
|
28143608 |
2017 |
Diffuse Large B-Cell Lymphoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Interestingly, there were several normal (eg germinal centre centroblasts and monocytoid B-cells) and malignant B-cell populations (eg a proportion of diffuse large B-cell lymphomas, DLBCLs) that were Ig-negative, despite their BOB.1/OBF.1 and Oct2 expression.
|
14694522 |
2004 |
Diffuse Large B-Cell Lymphoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
In addition to their different clonal origin, Reed-Sternberg cells of Hodgkin's disease expressed a CD15+, CD20+ (rare cells), CD30+, Oct-2-, EBNA2-, LMP1+ phenotype, whereas anaplastic and Reed-Sternberg-like cells of diffuse large B-cell lymphoma were CD15-, CD20+, CD30+, Oct-2+, EBNA2+, and LMP1+.
|
12459631 |
2002 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
Overall, this study indicated that miR-489-3p and miR-630 function as oncotherapy-obstructing microRNAs by directly targeting OCT2 in RCC.
|
31649850 |
2019 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
Previous studies have shown that loss of the human organic cation transporter OCT2 is the main factor contributing to oxaliplatin resistance in RCC, and that DNA hypermethylation and histone methylation play important roles in the transcriptional repression of <i>OCT2</i> in RCC.
|
31088315 |
2019 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.030 |
PosttranslationalModification
|
disease |
BEFREE |
Epigenetic analysis revealed that the repressed OCT2 promoter in RCC is characterized by hypermethylated CpG islands and the absence of H3K4 methylation.
|
27440728 |
2016 |
Diabetes Mellitus, Insulin-Dependent
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We detected nominal evidence of association (P < 0.05) between the SLC22A2 (SNPs rs653753, rs596881, and rs316019) and SLC22A3 (SNPs rs376563, rs2048327, rs2457576, and rs1567438) genes and DN and hypertension in Finnish men with T1DM.
|
20429798 |
2010 |
Diabetes Mellitus, Insulin-Dependent
|
0.020 |
Biomarker
|
disease |
BEFREE |
SLC22A2 and SLC22A3, two genes downstream of IGF2R that are imprinted in the mouse, showed no T1D association.
|
15531531 |
2004 |
Multiple Myeloma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Oct2 should be explored as a potential selective therapeutic target in myeloma.
|
21438833 |
2011 |