Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Finally, the effect of miR-27a on tumorigenesis and microvessel density (MVD) was analysed after xenograft tumour inoculation in nude mice.
|
31724333 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, recent studies show that miR-27a pays an important role in epithelial-mesenchymal-transition, regulating tumor immune response, and chemoresistance.
|
31572683 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The diagnostic efficacy for miR 27a was superior to both tumor markers for early detection of BC especially high-risk BC groups.
|
31145011 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In this review, we discuss the role of miR-27a in tumor biology and clinical significance in detail and offer novel insights into molecular targeting therapy for human cancers.
|
31258791 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
miR-27a-3p Functions as a Tumor Suppressor and Regulates Non-Small Cell Lung Cancer Cell Proliferation via Targeting HOXB8.
|
31319766 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, the present study demonstrated that the effects of miR-27a-3p on colon cancer cell proliferation and apoptosis were similar to those of the tumor suppressor gene BTG1.
|
31452761 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The expression levels of miR-27a and miR-31 are related to distant metastasis and tumor grade of patients with colorectal cancer, and positively associated with the survival time of patients, having high diagnostic value.
|
31452786 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-27a-3p (miR-27a-3p) was a tumor oncogene in various cancers.
|
31410369 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Insulin treatment of the human granulosa-like tumor cell line (KGN) resulted in decreased downregulated expression of miR-27a-3p, and this effect appeared to be mediated by signal transducer and activator of transcription STAT1 and STAT3.
|
29029022 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Dual luciferase assay indicated tumor suppressor FOXO1 was a direct target of miR-27a.
|
30138596 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results suggest that miR-27a acts as a tumor suppressor in cervical cancer, especially in adenocarcinoma, by inhibiting TGF-βRI signaling pathway.
|
29531222 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Overall, miR‑27a exhibits an essential role in tumor development and progression in TNBC and may be used as a potential biomarker to predict radiotherapy response and prognosis for the disease.
|
29115608 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings contribute to current understanding of the functions of miR-27a-3p and suggest a mechanism by which miR-27a-3p plays an anti-tumor role in the development of HCC by targeting DUSP16.
|
29143999 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The expression of serum miR-27a in liver cancer patients with higher tumor-node-metastasis (TNM) staging (stage III-IV, number of tumors >1, tumor size >5 cm, and vascular invasion) was significantly higher than those in patients with lower TNM staging (stage I-II, number of tumors =1, tumor size ≤5 cm, and no vascular invasion) (p<0.05).
|
30229820 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, oncogenic miR-27a inhibits AP-2β expression by binding to the AP-2β 3' untranslated region (UTR) and reverses the tumor suppressive role of AP-2β.
|
30026878 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
However, the altered cellular context averts miR-27a-5p from successfully accomplishing its tumor suppressive function at this stage of disease.
|
29415999 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Consistently, down-regulation of miR-27a inhibited the growth and metastasis of engrafted tumors in vivo.
|
28327189 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-27a (miR-27a) has been reported to be an onco-microRNA in multiple cancers promoting tumor growth and metastasis, but the role of miR-27a in regulating the cancer sensitivity to chemotherapy remains unknown.
|
26662313 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, miR-27a functions as a tumor suppressor by suppressing MAP2K4 which acts as an oncogene in prostate cancer cell lines; we also provided a new mechanism of castration-resistant prostate cancer mediated by miR-27a that downregulation of miR-27a caused by aberrant AR signaling and PI3K/Akt signaling after androgen deprivation therapy (ADT) would promote the progression of castration-resistant prostate cancer.
|
27594411 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In the RT-qPCR based validation experiments, no significant difference between tumour and stroma/normal rectal mucosa was detected for the mean of the normaliser candidates miR-27a, miR-193a-5p and let-7g (first validation P = 0.801, second validation P = 0.321).
|
26937645 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Multivariate Cox proportional hazards model analysis showed that low expression of miR-26a and high expression of miR-27a (P = 0.021; P = 0.011), high TNM stage (P = 0.001; P = 0.003), tumor grade (P = 0.005; P = 0.01), and distant metastasis.
|
26377680 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We demonstrated that CBFA2T3 is downregulated in majority of OS samples and its over expression significantly attenuated OS metastatic process mediated by miR-27a/miR-27a* underscoring CBFA2T3 functions as a tumor suppressor in OS.
|
25749032 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, we demonstrated in a mouse xenograft model that both curcumin and AKBA treatments suppressed tumor growth, which corresponded with alterations in the expression of miR-34a and miR-27a, consistent with our in vitro findings.
|
25712055 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, miR-27a was shown to be a significant tumor suppressor by targeting and decreasing PHB protein expression in glioma U251 cells. miR-27a targeting of PHB may be a novel potential therapeutic strategy for glioma.
|
25777779 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Inhibition of MIR21, MIR23A, and MIR27A had synergistic effects in reducing proliferation of PDAC cells in culture and growth of xenograft tumors in mice.
|
24120476 |
2014 |