Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, upregulation of miR-141 inhibited the tumor growth and lymph node metastasis in vivo.
|
31629025 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor cell xenografts in nude mice were conducted to observe the effect of miR-141-3p on trastuzumab resistance in breast cancer cells in vivo.
|
31087707 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In contrast, GP73 was negatively correlated with miR-141-3p in HCC tumors.
|
30695725 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-141-3p functions as a tumor suppressor through directly targeting ZFR in non-small cell lung cancer.
|
30611568 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We found that miR-141 (TE) correlated significantly to Gleason score ≥8 (p = 0.040) and large tumor size (≥20 mm, p = 0.025) and miR-141 (TE + TS) to Gleason grade (p = 0.001).
|
30674952 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Although miR-141 has been demonstrated to primarily function as a tumor suppressor in numerous malignancies, including glioblastoma, the mechanisms involved remain poorly understood.
|
31522595 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, miR-141-3p acts as a tumor suppressor, via directly targeting TRAF5 and indicated miR-141-3p might be a potential therapeutic target for colorectal cancer.
|
31078266 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
<i>In vivo</i> studies also demonstrated that exogenous overexpression of miR-141 in BGC-823 cells markedly reduced tumor growth in nude mice.
|
31289535 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results suggest that miR-141 functions as a tumor suppressor in HNSCC and that it suppresses tumor growth and metastasis by suppressing EGFR signaling.
|
30737360 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
NRP-1 depletion suppressed tumor growth and liver metastasis and miR-141 mimics inhibited the growth of established tumors in mice.
|
31572065 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The present study aimed to investigate whether miR-141 is a tumor suppressor or oncogenic when it reaches normal levels in chitosan/miR-141 nanoplexes.
|
31389101 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
<i>TP53, KRAS, APC</i>) has limited diagnostic sensitivity (40-60%), however, methylated DNA including <i>SEPT9, SFRP1, SDC2</i> can be applied with higher sensitivity (up to 90%) for CRC.Circulating miRNAs (e.g. miR-21, miR-92, miR-141) provide comparably high sensitivity for CRC as the circulating tumor cell mRNA markers (e.g.EGFR, CK19, CK20, CEA).
|
31046485 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, the findings suggested that miR-141-3p can act as a tumor suppressor in PTC and may be a potential therapeutic target for PTC treatment.Anat Rec, 302:258-268, 2019.
|
30290400 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
There was also a positive correlation between the percentage of PD-L1-positive tumor cells and the expression levels of miR-141 (R=0.441; P=0.0024), miR-200b (R=0.372; P=0.011) and miR-429 (R=0.430; P=0.0028), and between the percentage of the tumor area with immune cell infiltration and the expression levels of miR-141 (R=0.333; P=0.03) and miR-200b (R=0.312; P=0.046).
|
31186735 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Consistent up-regulation in tumor tissue was found for miR-141 and miR-330.
|
30972782 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Enforced expression of FOXA2 blocked the effects of miR-141-3p on cervical cancer cell proliferation and invasion. miR-141-3p overexpression significantly accelerated the growth of xenograft tumors, which was accompanied by a striking reduction in FOXA2 expression. miR-141-3p acts as an oncogene in cervical cancer largely through repression of FOXA2.
|
30222949 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, restoration of miR-141 in c-Myc knockdown NPC cells notably rescued the effect of c-Myc on cell proliferation and tumor growth, as well as the blocking of PTEN/AKT pathway.
|
29559001 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Mechanistic studies identified that BMI1 served as the direct target of miR-141, and overexpression of BMI1 reversed the tumor repressor effect of miR-141.
|
30405786 |
2018 |
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 |
It was also revealed that exogenous miR‑141 expression resulted in in vivo inhibition of tumor growth and inhibition of the development of VM.
|
29901110 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
WIPF1 antagonizes the tumor suppressive effect of miR-141/200c and is associated with poor survival in patients with PDAC.
|
30041660 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our results suggest that miR-141 employs multiple mechanisms to obstruct tumour growth and metastasis.
|
28112170 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, decreased miR-141-3p levels were detected in the multiple tumor nodes group ( P = .004), the metastasis group ( P < .001), and the advanced TNM stage group ( P = .01), compared to the single tumor nodes group, the nonmetastasis group, and the early TNM stage group.
|
28436261 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Downregulation of miR-141 expression correlated with tumor stage, lymph node involvement, and expressions of PCNA, Ki67, and HER2.
|
28220627 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In addition, a Cox regression model was used to examine whether miR-141 was a potential biomarker of glioblastoma. miR-141 was aberrantly downregulated in glioblastoma cell lines and human glioblastoma tumors.
|
28943957 |
2017 |