Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The subcutaneous and metastases tumor models were employed to study the effects of miR-22 on cell proliferation and metastasis of breast cancer cells in vivo.
|
30502362 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings showed that miR-22 served as a tumor suppressor in melanoma progression, implying that miR-22 may function as a novel therapeutic target and prognostic biomarker for melanoma treatments.
|
31298385 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
And besides that, elevated expression of miR-22 was negatively correlated with TNM stage, lymph node metastasis, distant metastasis and recurrence, while no significant association was found between microRNA-22 expression and T stage, tumor differentiation, and lymphatic invasion.
|
31632145 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Interestingly, miR-22 played an important role as a tumor suppresser on suppressing cell proliferation, migration and cell-cycle progression of OSCC cells.
|
29385191 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We demonstrated that miR-22 directly bound to the 3'-UTR of HuR and led to inhibition of HuR protein, which repressed CRC proliferation and migration in vitro and decelerated CRC xenografted tumour growth in vivo.
|
29351796 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These findings indicated that EZH2 facilitates galectin-9 expression by epigenetically repressing miR-22 and that galectin-9, which is known as an immunosuppressant, also functions as a tumor suppressor in HCC.
|
29316949 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-22 was previously reported to act as a tumor suppressor or oncomiRNA in various types of cancer.
|
29434190 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Recently, microRNA-22 (miR-22) has been reported to be a cancer-related miRNA in several types of tumors.
|
29319163 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Overexpression of DGCR5 was able to reverse the tumor inhibitory effect of hsa-mir-22-3p mimics.
|
29030962 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-22 acts as tumor suppressor by inhibiting proliferation and migration, and by inducing apoptosis of cervical cancer cell lines by targeting the 3'UTR of HDAC6.
|
30379969 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our results then demonstrated that microRNA-22 functioned as a tumor suppressor microRNA and indicated potential application for the diagnosis and treatment of cancer in the future.
|
30384806 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Moreover, overexpression of miR-22 could significantly inhibit the HCC cell proliferation, migration and invasion in vitro and decrease HCC tumor growth in vivo.
|
28184176 |
2017 |
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 |
AlteredExpression
|
group |
BEFREE |
Acidosis triggered upregulation of tumor promoting miR-125b in AN3-CA cell (type II EC), whereas in Ishikawa cells (type I EC) miRNAs with tumor suppressive function were found altered in divergent directions, both up- (let-7a) and down- (miR-22) regulated.
|
28627686 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
miR-22 has been shown to be frequently downregulated and act as a tumor suppressor in multiple cancers including breast cancers.
|
28882183 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings showed that miR-22 functioned as tumor suppressor in RCC and blocked RCC growth and metastasis by directly targeting SIRT1 in RCC, indicating a potential novel therapeutic role in RCC treatment.
|
26499759 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our systematic analysis establishes miR-22 as a novel regulator of tumour cell metabolism, a function that could contribute to the role of this miRNA in cellular differentiation and cancer development.
|
26477310 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, lower miR‑22 expression levels were associated with histological grade, tumor stage and lymph node metas-tasis.
|
27082730 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Additionally, we confirmed the higher ACLY protein levels and the lower miR-22 expressions in hundreds of clinical samples of the four primary tumors, and a negative correlation relationship between ACLY and miR-22 was clarified.
|
27317765 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-22 was decreased and acted as a tumor suppressor in melanoma, and MMP14 and Snail were the functional targets of miR-22.
|
27564100 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Moreover, restoring miR-22 expression blocked tumor growth and prevented tumor dissemination in vivo Gene expression profiling analysis of miR-22-expressing cells suggested TACC1 and RAB5B as possible direct miR-22 targets.
|
27569217 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
miR-22 has a potent anti-tumour role with therapeutic potential in acute myeloid leukaemia.
|
27116251 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The down-expression of miR-22 can regulate cell growth and motility in TSCC cells, which indicates that miR-22 acts as a tumor suppressor in TSCC.
|
26943814 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We also observed that the Gal-9/miR-22 axis may influence lymphocyte apoptosis and tumor cell proliferation.
|
26239725 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our data suggest that miR-22 functions as a tumor suppressor and is a promising prognostic biomarker in breast cancer.
|
25304371 |
2015 |