Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
E2F3, a member of the E2F family, plays a critical role in cell cycle and proliferation by targeting downstream, retinoblastoma (RB) a tumor suppressor family protein.
|
31839743 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Taken together, these results suggest that miR‑210‑3p may act as a tumor suppressor in ovarian cancer cells and affect the sensitivity of cells to cisplatin by directly targeting E2F3.
|
30957179 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results indicate a tumor suppressor role for miR-200c in renal cancer cells via the direct targeting of Bmi-1 and E2F3.
|
28413473 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
E2F3 upregulation promotes tumor malignancy through the transcriptional activation of HIF-2α in clear cell renal cell carcinoma.
|
28903320 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In summary, these findings identify E2f3 as a key transcription factor in TAMs, which influences the tumor microenvironment and tumor cell metastasis.
|
26549026 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results suggested that miR-203 may function as a tumor suppressor in glioma progression and that the miR-203/E2F3 axis may be a novel candidate in the development of rational therapeutic strategies for glioma.
|
25515700 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results revealed a tumor suppressive role for miR-429 in renal cell carcinoma through directly targeting BMI1 and E2F3.
|
25953723 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Silencing of E2F3 suppresses tumor growth of Her2+ breast cancer cells by restricting mitosis.
|
26512919 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, our study demonstrated that miR-34c plays a role of tumor suppressor in HEC-1-B cells, and E2F3 protein may be a target of miR-34c.
|
25846116 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
This study confirmed a novel miR-34a-E2F3-survivin axis in the tumor suppressor role of miR-34a in cervical cancer.
|
25675046 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-424 inhibits Akt3/E2F3 axis and tumor growth in hepatocellular carcinoma.
|
26315541 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Moreover, E2F3 overexpression partially attenuated the tumor suppressive effects of miR-144, and the expression of E2F3 was negatively correlated with miR-144 level in HCC tissues.
|
25073510 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In Rb;p107-deficient retinae, E2f1 and E2f3 inactivation rescued tumor formation but only E2f1 rescued the retinal development phenotype.
|
25338120 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Further studies revealed that E2F3 was a direct target of miR-449a in lung cancer cells. miR-449a also suppressed tumor formation in vivo in nude mice.
|
24211326 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, our data indicate that E2F3 is a key regulator of cell proliferation in a subset of bladder cancer and the 6p22.3 amplicon is a biomarker of aggressive phenotype in this tumor type.
|
24231253 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The preliminary data indicate that E2F3 is frequently expressed in pediatric Wilms' tumors examined in the present study.
|
24210184 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
High module scores of chromosomal instability, phosphatase and tensin homolog (PTEN) loss, and E2F3 transcription factor were associated with increased pCR probability in estrogen receptor (ER) -negative/human epidermal growth factor receptor 2 (HER2) -negative and ER-positive/HER2-negative but not in HER2-positive tumors (interactions between HER2 and each of these modules for their association with pCR: P < .05; FDR, 0.17; trend for interaction between HER2 and PTEN).
|
22508827 |
2012 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
When compared with healthy control tissue, both E2F3 isoforms were overexpressed in the cancers, but only E2F3a expression correlated with tumor stage (ρ=0.349, P=0.0001) and residual disease (ρ=0.254, P=0.004).
|
21516127 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor latency decreased in the E2F1 mutant background and significantly increased in both the E2F2 and E2F3 mutants.
|
21245101 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Genes in the BRCA1 preneoplastic signature included several known tumor suppressor genes such as CDKN1C and EFEMP1 and several thought to be important in invasion and metastasis such as E2F3.
|
21170264 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results, together with the prior demonstration of augmentation of microtubule-related genes by E2F3, suggest that enhanced taxane sensitivity in tumors with high YY1/E2F activity may be mediated by modulation of putative target genes with microtubule function.
|
19208743 |
2009 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Chemotherapy-treated tumors showed a significant decrease in KIF14 and E2F3 expression compared to untreated tumors (p<0.01 and 0.001, respectively).
|
19190782 |
2009 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Whereas the absence of E2F1 and E2F3 function has no impact on Myc-mediated tumor development, the absence of E2F2 substantially accelerates the time of tumor onset.
|
19749980 |
2009 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Genes involved in the E2F3 pathway are associated with chemotherapy sensitivity among ER- tumors.
|
18445275 |
2008 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Gene-specific quantitative multiplex polymerase chain reaction of candidate oncogenes at 1q32.1 (KIF14), 6p22 (E2F3 and DEK), and tumor suppressor genes at 16q22 (CDH11) and 17q21 (NGFR) showed the most common gene gains in RB to be KIF14 in cell lines (80%) and E2F3 in primary tumors (70%).
|
17099872 |
2007 |