Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Thus, in prostate cancer, CtBP1-regulated miR-34a modulates STMN1 expression and is involved in cancer progression through the CtBP1miR-34aSTMN1GDF15 axis.<b>Implications:</b> The CtBP1miR-34aSTMN1GDF15 axis is a potential therapeutic target for treatment of aggressive prostate cancer.<i></i>.
|
29025958 |
2018 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
High STMN1 Expression is Associated with Cancer Progression and Chemo-Resistance in Lung Squamous Cell Carcinoma.
|
28933054 |
2017 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Stathmin 1 (STMN1) is a major cytosolic phosphoprotein regulating microtubule dynamics, thereby playing an important role in cancer progression and resistance to microtubule-binding anticancer agents.
|
28350065 |
2017 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Thus, STMN1 is likely to support cellular processes essential for tumor progression: survival and migration.
|
25791566 |
2015 |
Tumor Progression
|
0.100 |
PosttranslationalModification
|
phenotype |
BEFREE |
STMN1 activities are regulated through phosphorylation-dephosphorylation mechanisms that control assembly of the mitotic spindle, and dysregulation of STMN1 phosphorylation is associated with mitotic aberrancies leading to chromosome instability and cancer progression.
|
26466335 |
2015 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
STMN1 contributes to a poor prognosis and cancer progression in EHCC patients.
|
24708177 |
2014 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Stathmin is a p53-target gene, frequently overexpressed in late stages of human cancer progression.
|
23610071 |
2013 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Stathmin is overexpressed in a variety of assessed human malignancies and is correlated with tumor progression and poor prognosis.
|
19786090 |
2010 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Stathmin expression correlates with hepatocarcinogenesis and tumor progression.
|
20204289 |
2010 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Stathmin expression correlates with cervical carcinogenesis and tumor progression.
|
19034510 |
2009 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
In addition, through a combination of proteomics and immunological methods, this study demonstrates that stathmin 1alpha, a cytoskeletal protein implicated in tumor progression, undergoes a basic isoelectric point shift (p I) following uPAR suppression, suggesting that post-translational modification of stathmin occur secondary to uPAR suppression.
|
18808175 |
2008 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Here we demonstrate cytoplasmic overexpression of stathmin in premalignant lesions (dysplastic nodules; DNs) and hepatocellular carcinomas (HCCs), which significantly correlated with tumor progression, proliferation, and activation of other protumorigenic factors (e.g., nuclear p53).
|
17663418 |
2007 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Stathmin overexpression cooperates with p53 mutation and osteopontin overexpression, and is associated with tumour progression, early recurrence, and poor prognosis in hepatocellular carcinoma.
|
16739096 |
2006 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
These results suggest that expression of stathmin could contribute to cancer progression/prognosis, and that stathmin may have potential as a biomarker and a therapeutic target for OSCC.
|
16495930 |
2006 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Finally, we find that M68 lies within a four-gene cluster that includes a novel helicase-like gene (NHL) related to RAD3/ERCC2, a plasma membrane Ras-related GTPase and a member of the stathmin family, amplification or overexpression of which may also contribute to cell growth and tumor progression.
|
10655513 |
2000 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Taken altogether, the results suggest that up-regulation Op18 levels in leukemia/lymphoma cells are strongly associated with, but not a direct cause of tumour progression.
|
8464235 |
1993 |