Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Mts1 is a member of the S100 protein family and is involved in tumor progression and metastasis.
|
31467231 |
2020 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
In a mouse model of in situ gene therapy, a single intratumoral treatment with the bicistronic vector conferred markedly inhibited tumor progression while the treatment with either CDKN2A or p53 alone only partially controlled tumor growth.
|
31439890 |
2020 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
CSN6 promoted the loss of p16-mediated tumor progression and played an important role in regulating ubiquitin-independent proteasomal degradation of p16.
|
31565481 |
2019 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
P16 is the product of cyclin-dependent kinase 2 (CDKN2A) gene and plays multi-pronged roles in the cancer progression.
|
29388151 |
2018 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
The accumulation of cyclin-dependent kinase inhibitor 2A (p16<sup>ink4a</sup> ) protein in a cell is associated with neoplastic progression in precancerous cervical lesions.
|
27926800 |
2017 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
This tumor progression is associated with a loss of 53BP1 and p16 expression.
|
29047390 |
2017 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
The p14ARF/MDM2/ TP53 pathway is known to play an important role in tumor progression by cell cycle control, although the association between this pathway and the prognosis of esophageal squamous cell carcinoma (ESCC) is unclear.
|
27414035 |
2016 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
By contrast, in advanced stages of Kras-driven murine PDAC, loss of p53 or p16 was associated with senescence bypass, and RelA deficiency in this context attenuated cancer cell proliferation and prolonged mouse survival, indicating that RelA enhances tumor progression in established PDAC.
|
27454293 |
2016 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
HPV infection appears to be involved in cancer progression in SQC by promoting the expression of p53; however, p16 cannot be used as a surrogate marker for HPV infection in SQC.
|
25544708 |
2015 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
p14 expression seems to increase initially in early breast cancer and decrease with further tumour progression. p14 may be induced to counteract immortalisation and hTERT surge.
|
23645774 |
2013 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Our results demonstrate for the first time a pro-migratory role for p16, and suggest a potential mechanism for the observed association between cytoplasmic p16 and tumor progression in diverse tumor types.
|
23894465 |
2013 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
The results suggest that strong p16 expression in the villous mesenchyme may be responsible in part of the morbidity of the moles, and the key of cancer progression in the choriocarcinomas would be a fast cell-cycle turnover.
|
23065465 |
2013 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
AP4 achieves this effect by direct repression of p16 and p21, and may thereby critically contribute to c-MYC function and tumor progression.
|
23949224 |
2013 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Moreover, we reconstructed the phylogeny of the fragments for each patient, identifying copy number alterations in EGFR and CDKN2A/B/p14ARF as early events, and aberrations in PDGFRA and PTEN as later events during cancer progression.
|
23412337 |
2013 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Consistently, ARF expression occurred at a later stage of tumor progression than activation of the DDR or p16(INK4A), a tumor-suppressor gene overlapping with ARF.
|
23852374 |
2013 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
The dose-dependent upregulation of endogenous FOXM1 (isoform B) expression during tumour progression across a panel of normal primary NOK strains (n = 8), dysplasias (n = 5) and head and neck squamous cell carcinoma (HNSCC) cell lines (n = 11) correlated positively with endogenous expressions of HELLS, BMI1, DNMT1 and DNMT3B and negatively with p16(INK4A) and involucrin.
|
22461910 |
2012 |
Tumor Progression
|
0.100 |
PosttranslationalModification
|
phenotype |
BEFREE |
These results imply that promoter hypermethylation of p16 occurs at an early stage of cervical neoplastic progression.
|
21436693 |
2011 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
However, it has also been shown that an elevated level of expression (upregulation) of P16 is involved in cellular senescence, aging, and cancer progression, indicating that the regulation of P16 is critical for its function.
|
21619050 |
2011 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Low expression of the nuclear p16INK4A form and strong expression of the cytoplasmic p16INK4A form both represent two independent parameters each associated with tumour progression in GISTs.
|
20459531 |
2010 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Ink4a/Arf and oncogene-induced senescence prevent tumor progression during alternative colorectal tumorigenesis.
|
20708155 |
2010 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
The degree of tumor progression (such as growth, angiogenesis, and metastasis) directly correlates with the expression of vascular endothelial growth factor (VEGF), but inversely correlates with the expression of tumor-suppressor gene p16, therefore we examined whether the restoration of p16 in breast cancer cells would modulate VEGF expression.
|
20307196 |
2010 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
EGFR and p16INK4a can be used for early diagnosis and E-cadherin for cancer progression and cell migration.
|
20937225 |
2010 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
This study validates a role for Met activation in melanoma tumor progression in the context of Cdkn2a deficiency.
|
19422607 |
2009 |
Tumor Progression
|
0.100 |
GeneticVariation
|
phenotype |
BEFREE |
The p73 and p16 polymorphic genotypes were significantly associated with shorter time to tumor progression (log-rank test, P = 0.021 and P = 0.039, respectively).
|
19020940 |
2009 |
Tumor Progression
|
0.100 |
PosttranslationalModification
|
phenotype |
BEFREE |
P16(INK4a) methylation and gamma-tubulin gene amplification had a synergistic effect on tumor progression.
|
19131428 |
2009 |