Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In addition, our data indicated that the inhibition or knockdown SMYD2 inhibit tumor sphere formation and reduce cell migration in NSCLC/CDDP cells, but not in NSCLC parental cells.
|
31106145 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, SMYD2 mRNA expression levels were associated with the RFS of patients with BC with metastatic relapse, and SMYD4 may serve as a tumor suppressor in patients with BC, as patients with increased SMYD4 mRNA expression levels had significantly better RFS compared with decreased SMYD4 mRNA expression levels.
|
30930987 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
High SMYD2 expression correlated with a high TNM stage (P = 0.007) and early tumor relapse (P = 0.032).
|
31754403 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Silencing of SMYD2 by RNAi in triple-negative breast cancer (TNBC) cell lines or inhibition of SMYD2 with its specific inhibitor, AZ505, significantly reduced tumor growth in vivo.
|
29487338 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Using 2 PTC cell lines, K1 and B-CPAP, we demonstrated that high expression of SMYD2 can promote tumor cell proliferation.
|
30319138 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Positive expression of SMYD2 was correlated with tumor size, vascular invasion, differentiation and TNM stage (<i>P</i> < 0.05).
|
29344279 |
2018 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
Our results shed light on a novel mechanism that modulates the kinase activity of the ALK fused gene product and imply that SMYD2-mediated ALK methylation might be a promising target for development of a novel class of treatment for tumors with the ALK fused gene.
|
28370702 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In nonmultiple cases, patients with SMYD2-overexpressing tumors had a worse overall survival rate than did those with nonexpressing tumors (P = .017, log-rank test), and SMYD2 positivity was independently associated with overall survival in the multivariate analysis (P = .003).
|
26826421 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Finally, we show that inhibition of SMYD2 cooperates with standard chemotherapy to treat PDAC cells and tumors.
|
26988419 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings suggest that SMYD2 has a crucial role in tumor cell proliferation by its overexpression and highlight its usefulness as a prognostic factor and potential therapeutic target in gastric cancer.
|
25321194 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Low expression levels of SMYD2, SETD3, and NO66 were significantly associated with shorter disease-specific and disease-free survival, especially in patients with non-organ confined tumors.
|
26488939 |
2015 |