Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-122 has been regarded as a tumor suppressor.
|
31477445 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-122 (miR-122) acts as a tumor suppressor in a variety of cancers and has been found to be dominant in gastric adenocarcinoma.
|
31828293 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumors in mice treated with miR-122 mimics demonstrated a mean ± SD 763- ± 60-fold increase in miR-122 levels compared with tumors in the control group.
|
31225651 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We also verified that ALDOA was the direct target of miR-122, and the tumor suppressive effects caused by DIO3OS knockdown or miR-122 overexpression could be rescued by re-expression of ALDOA in PC cells.
|
31384177 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, in vivo experiments demonstrate that the GOA/miR-122 NPs exhibit higher tumor accumulation.
|
31733293 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Collectively, the results of this study revealed that LINC01296 is a tumor promoter that can promote the migration and invasion of HCC cells through EMT, while miR-122-5P is involved in the underlying mechanisms.
|
30988624 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The present results indicate that miR‑122 serves a tumor‑promoting role by direct targeting FOXO3 in ccRCC.
|
30483771 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our data suggested that miR-122-5p functions as a tumor suppressor and may be a therapeutic target for NPC.
|
30720170 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our data indicate that up-regulation of miR-122 promotes cell survival in acquired radioresistant breast cancer and also suggest that miR-122 differentially controls the response to radiotherapy by a dual function as a tumor suppressor an and oncomiR dependent on cell phenotype.
|
30938061 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Hence, COP inhibited the proliferation, migration and promoted apoptosis of HCC cells; moreover, it inhibited the tumor growth in nude mice by up-regulating the expression of miR-122.
|
29710498 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
It was observed that low expression of miR‑122 and high expression of TRIM29 led to a low overall survival rate in patients with NPC, which was associated with tumor‑node‑metastasis (TNM) stage and distant metastasis of NPC.
|
29693120 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In vivo experiment demonstrated that ANRIL knockdown impeded tumor growth in vivo and increased miR-122-5p expression.
|
29127494 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The average expression level of miR-122-5p was decreased in HCC patients compared with controls from TCGA database (P<0.001), and the downregulation of miR-122-5p was significantly associated with HCC tissues (P<0.001), tumor vascular invasion (P<0.001), metastasis (P=0.001), sex (P=0.006), virus infection status (P=0.001) and tissue (compared with serum; P<0.001) in cases from the GEO database.
|
30546424 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-122 functions as a tumor suppressor by inhibiting proliferation and inducing apoptosis, which is achieved by directly targeting RUNX2.
|
30070328 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The expression levels of exosomal miR-122 before TACE were shown to correlate significantly with aspartate aminotransferase (r=0.31, P=0.004) and alanine aminotransferase (r=0.33, P=0.003) levels, tumor diameter (r=0.29, P=0.010) and Child-Pugh score (r=-0.28, P=0.013).
|
30127924 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
By down-regulating ALDOA, overexpression of miR-122-5p appeared to promote cell apoptosis and significantly inhibit cell proliferation, invasion in vitro and suppress the tumor growth in vivo.
|
30121648 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-122-3p inhibits tumor cell proliferation and induces apoptosis by targeting Forkhead box O in A549 cells.
|
29434994 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Hsa-miR-122-5p (miR-122) has been reported with tumor-suppressing roles in various cancers.
|
30136751 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The miR-122 and miR-22 levels were negatively correlated with tumor size, lymph node metastasis, TNM stage, pathological type, differentiation grade, liver cirrhosis, AFP and HBV DNA, all of which were independent risk factors (p < 0.05).
|
28272709 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
AdVince includes the gene promoter from human chromogranin A for selective replication in neuroendocrine cells, miR122 target sequences for reduced liver toxicity, and a cell-penetrating peptide in the capsid for increased infectivity of tumor cells and optimized spread within tumors.
|
27442441 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
MiR-122 expression was closely correlated with tumor size, vascular invasion and American Joint Committee on Cancer (AJCC) stage of HCC patients.
|
28890291 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Finally, in this study, miR-122-5p was confirmed inhibiting tumor GC cells proliferation and inducing cells apoptosis by targeting MYC.
|
29442023 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
High miR-122 expression (> 100) was associated with early TACE refractoriness (within 1 year; HR, 2.77; 95% CI, 1.12-6.86; P = 0.028), together with tumor number (HR, 22.73; 95% CI, 2.74-188.66; P = 0.004) and tumor size (HR, 4.90; 95% CI, 1.99-12.06; P = 0.001).
|
27194671 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings suggest that miR-122 might function as a tumor suppressor in GC and could serve as a promising candidate for therapeutic applications regarding GC treatment.
|
28337380 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-122, an abundant and conserved liver-specific miRNA, regulates hepatic metabolism and functions as a tumor suppressor, yet systematic and direct biochemical elucidation of the miR-122 target network remains incomplete.
|
28735896 |
2017 |