Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The miR-200c overexpression significantly decreased the expressions of lncRNA HOTAIR and snail, but increased E-cadherin expression in the lentivirus-miR-200c transducted SKOV3 cells of xenograft tumor, compared with the negative control (P < .05).
|
31535411 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Importantly, miR-200c-led inhibition in cell growth and tumor development was prevented by forcing PDE7B transgene expression, while knockdown of PDE7B effectively inhibited cell growth.
|
30209363 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Therefore, overexpression of miR-200c might have therapeutic potential as an anticancer agent that inhibits tumor hypoxia.
|
31061665 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Correlation analysis showed that miR-200c expression was significantly associated with tumor size (P = 0.021), serum AFP level (P = 0.016), TNM stage (P = 0.019) and vein invasion (P = 0.026).
|
30962170 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Recent data suggest that the role of microRNA-200c in tumour pathogenesis is rather contradictory, and the underlying mechanisms by which microRNA-200c affects the carcinogenic potential of malignant cells remains unclear and requires further investigation at the molecular level.
|
31680118 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In multivariate analysis of the cases with localized disease, low miR200c expression in budding areas, but not at the tumor center, was an adverse tumor-specific survival factor (hazard ratio: 0.12; 95% confidence interval: 0.03-0.81; p = 0.02) independent of the clinical stage of the disease.
|
30206410 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Resistance to trastuzumab remains a major obstacle in HER2-overexpressing breast cancer treatment. miR-200c is important for many functions in cancer stem cells (CSCs), including tumour recurrence, metastasis and resistance.
|
31599500 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Overexpression of miR-200c-3p was considered a tumor suppressor and was found to significantly suppress the formation of migration and invasion in PCa cells via repression of E-cadherin-induced EMT.
|
31157262 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-200c promotes tumor cell proliferation and migration by directly targeting dachshund family transcription factor 1 by the Wnt/β-catenin signaling pathway in nasopharyngeal carcinoma.
|
30431444 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We also show that TA-III induces expression of tumor suppressive miR-200c and miR-141, which are negatively regulated by BMI1.
|
29528145 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
miR-200c, a tumor suppressor that modulate the expression of cancer stem cells markers and epithelial-mesenchymal transition in colorectal cancer.
|
29663476 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
IL-21-secreting hUCMSCs combined with miR-200c inhibit tumor growth and metastasis via repression of Wnt/β-catenin signaling and epithelial-mesenchymal transition in epithelial ovarian cancer.
|
29692616 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The results indicated that miR-200c overexpression and XIST knockdown could inhibit cell clone formation, self-renewal ability and EMT in BCSC-like cells. miR-200c knockdown could restore the tumour growth inhibition caused by XIST knockdown.
|
29559853 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
miR-21a negatively modulates tumor suppressor genes PTEN and miR-200c and further promotes the transformation of M2 macrophages.
|
29359349 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Serum level of miR-200c was lower in oral squamous cell carcinoma patients than that in healthy controls, and it was decreased with increased primary tumor stages.
|
30179745 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here we show a close negative correlation between SALL4 or PD-L1 and miR-200c in tumors from 98 patients with HBV-related hepatocellular carcinoma.
|
29593314 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The aberrant expression of miR-200c-5p and MAD2L1 was correlated with tumor stage, adjacent organ invasion and prognosis.
|
28609841 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Sulforaphane treatment resulted in a dose-dependent increase in the levels of tumor suppressive miR200c.
|
26879838 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Growing evidence suggests that metformin's anticancer effects are mediated at least in part by modulating microRNAs, including miR-200c, which has a tumor suppressive role in breast cancer.
|
28819383 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-200c achieves this oncogenic effect, at least in part, by targeting and inhibiting the tumor suppressor gene PTEN (phosphatase and tensin homolog), which is a key inhibitor of the AKT kinase signaling that promotes tumorigenesis in nasopharyngeal carcinoma.
|
28029649 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-200c regulates tumor growth and chemosensitivity to cisplatin in osteosarcoma by targeting AKT2.
|
29051585 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In vivo suppression of microRNA-200c level reduced tumor growth in mice.
|
28459373 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
No significant correlation was found between miR-200c expression in tumors or plasma and clinical characteristics.
|
28881640 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The miR-200c plays an essential role in tumor suppression by inhibiting epithelial-mesenchymal transition (EMT).
|
27918105 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Univariate survival analysis demonstrated that high miR-200c expression, positive lymph node metastasis and advanced Tumor-Node-Metastasis (TNM) classification stage significantly predicted decreased 5-year disease-free survival rates (all P<0.05) and poor 5-year overall survival rates (all P<0.01), respectively.
|
28943946 |
2017 |