Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We found that overexpression of miR-622 inhibited CRC angiogenesis in vitro, according to suppression of proliferation, migration, tube formation, and invasiveness of human umbilical vein endothelial cells (HUVECs) treated with a tumor cell-conditioned medium derived from Caco-2 or HT-29 cells.
|
30851425 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
It has recently been shown that miR-622 plays a tumor suppressive role in many human cancers.
|
28796324 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-622 plays as a tumor inhibitor in some types of cancer, however, its role in kidney cancer is unknown.
|
29507713 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results show that miR-622 acts as a tumor suppressor in thyroid cancer, at least in part, via targeting VEGFA, and suggest that miR-622 may serves as a potential target for treatment of thyroid cancer patients.
|
29593418 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We conclude that miR-622 is a novel tumor suppressor in melanoma and identify the miR-622-KRAS axis as potential therapeutic target.
|
29495114 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We applied quantitative polymerase chain reaction to determine the levels of miR-139-3p and miR-622 in 42 pairs of tumor and adjacent non-tumor tissues, and in serum samples of 117 patients and 90 control subjects.
|
28404964 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, we confirmed that miR-622 inhibited tumor proliferation and migration in vitro.
|
26333174 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings indicate that miR-622 may act as a tumor suppressor in ESCC and would serve as a potential therapy target for this disease.
|
27501502 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Overexpression of miR-622 suppressed tumor cell proliferation, migration, and invasion of A172, U87, and U251 cells.
|
26596833 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Ectopic expression of miR-622 led to a significant reduction of MAP4K4 expression in HCC cells and xenograft tumors.
|
26467022 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, miR-622 functions as a tumor suppressor by targeting K-Ras and impacting the anticancer effect of resveratrol.
|
22016468 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
More importantly, Lynch syndrome tumors displayed a unique miRNA profile compared with sporadic MSI tumors; miR-622, miR-1238, and miR-192 were the most differentially expressed miRNAs between these two groups.
|
21844009 |
2011 |