Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Finally, treatment of PTC cell line xenografts with thiostrepton resulted in growth inhibition of tumors in nude mice via down-regulation of FoxM1 and MMP-9 and MMP-2.
|
22049175 |
2012 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, high levels of MMP2 protein were positively correlated with the status of tumor size, lymph node metastasis, distant metastasis, Dukes' stage, and tumor invasion.
|
21968416 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Immunohistochemical evaluations of Ki-67 expression, as well as matrix metalloproteinase-2, -9, were found to be equal in BRAF-positive and BRAF-negative tumors.
|
25888143 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Mean levels for all investigated factors were significantly correlated with lymph node and hormone receptor status, while MMP-2 and TIMP-2 were correlated with tumor grade (P < 0.05).
|
17613170 |
2007 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
MMP-2 expression was enhanced with increased clinical stage and metastasis (P < 0.05), but was unrelated to patient age or tumor grade (P > 0.05).
|
24245968 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The most reliable method of IH examination appears to be direct MMPs-2/9 mRNA evaluation in tumor tissue; and MMP-2 evaluation in patients' serum is a valuable complement to it.
|
28601470 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Overexpression of MMP-2 is found to facilitate tumour propagation through the involvement of vascular endothelial growth factor (VEGF).
|
31012354 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Intravenous tail vein injection with Ad-MMP-2 on days 5, 9 and 11 after tumor implantation resulted in complete retention of neurological function as compared to control and scrambled vector (Ad-SV)-treated groups that showed complete paraplegia by day 14+/-2 days.
|
18292932 |
2008 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We investigate redox state-superoxide (SO) generation rate, activity of complex I in electron transport chain (ETC) of mitochondria and of dinitrosyl iron complexes by electron paramagnetic resonance; activity of matrix metalloproteinase (gelatinase) MMP-2 and MMP-9 by gel zymography of adipose tissues (AT) from 46 patients (64.0 ± 1.6 y.o.) with CRC (II-III stages, pT2-3N0-2M0) in the AT adjacent to tumor (ATAT) and at a distance of 3 cm from the tumor (ATD) to follow the connection of the AT redox state with some of the tumor microenvironment indicators.
|
30581847 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Supression of integrin alphaupsilonbeta6 inhibits the phosphorylation and nonphosphorylation level of ERK1/2, the secretion of uPA, pro-MMP-9 and pro-MMP-2 in tumor conditioned medium, and more important, inhibits MAPK-dependent [(3)H] labeled collagen IV degradation via the plasminogen activation cascade.
|
18566996 |
2008 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The prodrug vesicles were inert during the blood circulation, whereas they specifically accumulated and penetrated at the tumor site through matrix metalloproteinase-2 (MMP-2)-mediated cleavage of the PEG corona to achieve fluorescence-imaging-guided photodynamic therapy (PDT).
|
31793787 |
2020 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
ELISA, reverse transcription-PCR, and immunohistochemistry confirmed the increase of matrix metalloproteinase-2 proteins and mRNA in Slug overexpressed cells and xenograft tumors.
|
16299238 |
2005 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We show here using several invasive and non-invasive breast cancer cell lines that SAM inhibits global- and gene-specific demethylation induced by 5-azaCdR, prevents 5-azaCdR activation of prometastatic genes uPA and MMP2, resulting in inhibition of cell invasiveness while augmenting the growth inhibitory effects of 5-azaCdR and its effects on tumor suppressor genes.
|
23985780 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Matrix metalloproteinase -2 (gelatinase-A, Mr 72,000 type IV collagenase, MMP-2) and -9 (gelatinase-B, Mr 92,000 type IV collagenase, MMP-9) are key molecules that play roles in tumor growth, invasion, tissue remodeling, metastasis and stem-cell regulation by digesting extracellular matrix barriers.
|
27039800 |
2016 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Further analysis showed MMP2 rs243865 and MMP7 rs11568818 genotypes were associated with advanced tumor stages of cervical cancer patients.
|
26526578 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Here, we designed a cationic gene vector containing matrix metalloproteinase-2 (MMP2)-cleavable substrate peptides that specifically target tumor sites where MMP2 levels are high.
|
28043137 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor growth factor beta (TGFbeta) increased keratinocyte migration as well as both cell-associated and secreted MMP-2 production in wounded cell cultures.
|
10438572 |
1999 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Administration of crocin (100 mg/kg) hampered expression of tumor growth factor-β (TGF-β), α alpha smooth muscle actin (α-SMA) and collagen 1-α expression and significantly raised gene expression of matrix metalloproteinase-2 (MMP-2).
|
29740240 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Expression of CK19 and MMP-2 in tumor tissue was assessed through immunohistochemical staining of tissue microarrays (TMAs), which were constructed using samples from HCC patients with (n = 123) and without (n = 145) LNM.
|
21104440 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Serum Ang-2 and MMP-2 and tumor HIF-1α were identified as relevant baseline biomarkers of sunitinib activity in advanced RCC, warranting further research into their prognostic versus predictive value.
|
25100134 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
MMP-2 and MMP-9, members of the gelatinase protein family, are capable of degrading type IV collagen of basement membranes, and their overexpression is often associated with tumor aggressiveness and poor prognosis.
|
27569079 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Therefore, MMP‑2 and miR‑29b are tumor suppressor factors involved in ovarian cancer.
|
26099492 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Protease-triggered demasking would occur when the masked CPP reached the MMP-2/9-riched tumor.
|
28290666 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Western blot analysis revealed that the expression of p53 and MMP-2 protein in the tumor tissue after chemotherapy was significantly decreased.
|
30214563 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our review of the instrument validation data includes 1) tracking of Giant HeLa cells, which may be undergoing neosis, a process of tumor stem cell generation; 2) tracking the effects of cell cycle related toxic agents on cell lines; 3) using MicroRNAs to reverse the polarization state in macrophages to induce tumor cell killing; 4) development of liposomal nanoformulations to overcome Multi-Drug Resistance (MDR) in ovarian cancer cells; and 5) development of dual sensitive micelles to specifically target matrix metalloproteinase 2 (MMP2) over-expressing cell lines.
|
28371272 |
2017 |