Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-296 functions as a tumor suppressor in breast cancer by targeting FGFR1 and regulating the Wnt/β-catenin signaling pathway.
|
31841196 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, the findings demonstrated that miR-296-3p may function as a tumor suppressor, and inhibits the migration and invasion of NSCLC cells by targeting APEX1. miR-296-3p is therefore a potential therapeutic molecular modulator of NSCLC.
|
31402954 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings proved that miR-296-3p may play a role as a tumor suppressor in NSCLC both in vitro and in vivo, and we first reported that miR-296-3p can regulate the migration and invasion of A549 cells via targeting RABL3.
|
31298353 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The results demonstrated that miR-296 is a critical tumor suppressor which was downregulated in CRC patients.
|
30365090 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Bio-informatics prediction and our experiments validated that MMP-2 and MMP-9 were simultaneously targeted by miR-296-3p and FOXC1 promoter upstream transcript (FOXCUT); the latter two exerted tumor-suppressing effects on CMM cells by inhibiting cell proliferation, cell cycle progression, migration, invasion, and induction of cell apoptosis.
|
29260433 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results indicated that miR-296 may act as a tumor suppressor in cervical cancer by directly targeting SP1.
|
29241478 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Six pro-angiogenic miRNAs including miR-17-5p, miR-92a, miR-210, miR-20a, miR-18a, and miR-296 expressions were positively while 1 pro-angiogenic miRNA (miR-130a) was negatively correlated with tumor malignancy degree in GC patients.
|
30003708 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
This study aimed to identify mechanisms by which microRNA 296-3p (miR-296-3p) functions as a tumor suppressor to restrain nasopharyngeal carcinoma (NPC) cell growth, metastasis, and chemoresistance.
|
29525743 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Additionally, reduced miR‑296‑5p expression levels were correlated with tumor size, TNM stage and metastasis in HCC.
|
28586057 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
<b>Purpose:</b> This study was performed to identify the detailed mechanisms by which miR-296-3p functions as a tumor suppressor to prevent lung adenocarcinoma (LADC) cell growth, metastasis, and chemoresistance.<b>Experimental Design:</b> The miR-296-3p expression was examined by real-time PCR and <i>in situ</i> hybridization.
|
28751441 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Dysregulation of microRNAs (miRNAs) is actively involved in the pathogenesis and tumorigenicity of colorectal cancer (CRC). miR-296 was found to play either oncogenic or tumor suppressive role in human cancers.
|
28209128 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, the present findings indicate a role for miR‑296 as a tumor suppressor in pancreatic cancer through directly targeting AKT2, thus suggesting that miR‑296 may serve as a potential therapeutic target for the treatment of pancreatic cancer.
|
28534950 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Thus, our findings indicate that miR-296 exerts a tumor suppressive role in HCC and is a potential biomarker and drug-target.
|
27714806 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results show for the first time that miR-296-5p inhibits transcriptional mechanisms that support GBM SCs and identify a miR-296-5p:HMGA1:Sox2 axis as a novel regulator of GBM SCs and candidate pathway for targeting therapies directed at depleting tumors of their tumor-propagating stem cell subsets.
|
26898758 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Taken together, the present study indicated that miR-296-5p regulated PLK1 expression and could function as a tumor suppressor in NSCLC progression, which provides a potential target for gene therapy of NSCLC.
|
26549165 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our results show that the miR-296-5p/SCRIB axis plays a role in breast carcinogenesis and an miR-296-5p-based therapeutic approach hampers breast cancer tumour growth in vivo.
|
24527800 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-296-5p (miR-296-5p) functions as a tumor suppressor in prostate cancer by directly targeting Pin1.
|
24915000 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Numbl overexpression relies on loss of the tumor suppressor miRNA-296-5p (miR-296), which actively represses translation of Numbl in normal cells.
|
23440423 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Finally, miR-296 or Scrib levels predict tumor relapse in hepatocellular carcinoma patients.
|
21643016 |
2012 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Examining PC patient samples, we found an inverse correlation between HMGA1 and miR-296 expression: high levels of HMGA1 were associated with low miR-296 expression and strongly linked to more advanced tumor grade and stage.
|
21138859 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results suggest the existence of an altered microRNA expression pattern in PaCs together with a potential role of miR-296 as novel oncosuppressor gene in these neoplasia.
|
19926710 |
2010 |