Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These alterations in cell growth/survival properties were accompanied by induction of CDKN1B, a gene encoding the tumor suppressor p27.
|
31831170 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, it showed an elevating effect on the level of the tumor suppressor nuclear proteins P21 and P27 concentrations in MCF-7 cells.
|
31841673 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These effects appear to be mediated by the increase of p21 <sup>waf1</sup> and p27 <sup>Kip1</sup> , associated with a reduction of Cyclin D1 and Rb1 protein phosphorylation, and involve the downregulation of key molecules responsible for tumor development, that is, Notch1, Sox2, Stat3, and Survivin.
|
30701538 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings suggest that SOX2OT may act as a tumor promoter in PDAC through physically binding FUS and regulating its downstream cell cycle-associated factors CCND1 and p27.
|
31837005 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Treatment with LGSP resulted in a G1 phase cell cycle arrest in PC3 cells, which was further confirmed by decreasing the expression of cyclin D1 and CDK 4 and increasing the expression of the tumor suppressors p21 and p27.
|
30562012 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Thus, monitoring p27 localization and RhoB levels in non-small cell lung carcinoma patients appears to be a powerful prognostic marker for these tumors.
|
30206932 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Consistent with the in vitro findings, MYC expression was found to be reduced, while p27 expression was found to be elevated, and BIM expression and cleaved PARP levels were found to be increased in trametinib-treated xenograft tumors.
|
30788663 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We demonstrated a positive correlation between mRNA and protein expression of p27 and expression of key metastatic markers, vimentin, snail-2, β-catenin and stathmin-1 (STMN1) in patient tumors.
|
30992462 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
P27 is a putative tumor suppressor when located in the nucleus and AKT is an inhibitor of P27 which promotes growth of cholangiocarcinoma.
|
29428513 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In a xenograft mouse model implanted with PC-3-Pa cells, LJ-2618 (3 or 10 mg/kg) effectively inhibited tumor growth with the enhancement of Skp2 degradation and induction of p27 expression in tumor tissues.
|
30292755 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, TRMP is able to regulate cell proliferation, G1/S cell cycle progression, and tumor xenograft growth via the inhibition of p27.
|
30166522 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Notably, intratumor injection of therapeutic PSMD2 small interfering RNA effectively delayed xenograft tumor growth accompanied by p21 and p27 upregulation.
|
29777785 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In the tumors of p27+/mut rats, the wild-type <i>Cdkn1b</i> allele is neither lost nor silenced, implying that p27 is haploinsufficient for tumor suppression in this model.
|
29142006 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Pleckstrin homology domain leucine-rich repeat protein phosphatase 2 (PHLPP2) is a tumor suppressor that catalyzes the de-phosphorylation of the AGC kinases, while p27 acts as a tumor suppressor that regulates cell cycle, apoptosis, and cell motility.
|
29930380 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
TOP2A, Ki67, and cyclin D1, as categorical variables were not predictive, whereas cyclin D1 as continuous variable was predictive of trastuzumab benefit.<b>Conclusions:</b> In TransHERA, patients with HER2-positive early breast cancer with low p27 expression in their tumors benefited from trastuzumab treatment, whereas patients with high p27 expression did not.<i></i>.
|
29530933 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The present results revealed that genistein exerted its tumor suppressor effect at least partially via inhibition of Skp2 and promotion of its downstream targets p21 and p27.
|
29434697 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, forced depletion of p27 counteracts the tumor suppressive ability of PCBP1 in the same PCBP1 over-expressing cells.
|
30086790 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Polygodial, P3, and P27 all significantly decreased OSCC tumor growth, with P27 being equipotent with polygodial and P3 being the least efficacious.
|
30320372 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In PRL, the deficiency in p21 and p27 contributed to the tumor proliferation and migration and Cdk inhibitors may be used as a new therapeutic approach.
|
29230669 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We show that miR-203-HOTAIR interaction resulted in the inhibition of epithelial-to-mesenchymal transition (EMT) and metastatic genes as indicated by induction of key metastasis-suppressing proteins E-cadherin, claudin (epithelial markers), and PTEN along with induction of tumor suppressor genes p21 and p27.
|
29440295 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Skp2 (Fbxl1) directly binds to the tumor suppressor p27 in the context of the SCF<sup>Skp2</sup> E3 ubiquitin ligase to ubiquitylate and target-phosphorylated p27 for proteasomal degradation.
|
30108998 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In tumor xenografts of A431 cells, the conditional knockdown of PCTAIRE1 restores p27 protein expression and suppresses tumor growth.
|
28274513 |
2017 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Fifty-four percent of 50 CDKN1B mutation-negative tumors had a reduction of p27 nuclear staining.
|
27038812 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Ectopic miR‑940 accelerated cervical cancer cell growth, proliferation and cell cycle arrest in vitro as well as tumor formation in vivo. p27 and PTEN were evidenced as direct targets for miR‑940 and inhibition of p27 and PTEN recovered the suppressive function of miR‑940-silenced cell towards to proliferation and tumorigenicity in cervical cancer cells.
|
28350106 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The cell fate decision on TNA-nanoenvironment has been reported to possibly regulate proliferative activities via expression of p27 and BCL2 tumor suppressor proteins, cogent with SKP2 and BCL2 oncogenic proteins suppression.
|
28337249 |
2017 |