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 |
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 |
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 |
Collectively, this work reveals a direct link between the gain-of-function of mutant p53 and miRNA and uncovers a novel mutant p53-273H/miR-27a/EGFR pathway that has an important role in promoting tumor development.
|
23559009 |
2013 |
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 |
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 |
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 |
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 |
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 |
These data indicate that miR-27a contributes a tumor suppressor-like activity in acute leukemia cells via regulation of apoptosis, and that miR-27a and 14-3-3θ may be potential therapeutic targets.
|
23236401 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In vitro and in vivo functional validation in osteosarcoma cell lines confirmed the tumor suppressive role of miR-16 and the pro-metastatic role of miR-27a.
|
22350417 |
2012 |
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 |
Both in vitro and in vivo assays revealed that miR-27a attenuated ESCC proliferation, invasion and tumor growth in nude mice. miR-27a exerts its tumor suppressor function through inhibition of the KRAS-related ERK pathways.
|
24154848 |
2014 |
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 |
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 |
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 |
Biomarker
|
group |
BEFREE |
By integrated bioinformatic analysis and experimental confirmation, we identified MXI1, which has been found to act as a tumor suppressor gene by affecting c‑Myc, as a direct target of miR‑24‑3p and miR‑27a‑3p.
|
23254855 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, we propose that the miR27-FOXO1 tandem inhibits apoptosis and represents an alternative pathway for tumor cell survival in PIK3CA-nonmutated EEC.
|
24746199 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our study indicates for the first time that, in addition to its role in brain development, MCPH1 also functions as a tumor suppressor gene and is directly regulated by miR-27a.
|
25197360 |
2014 |
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 |
Biomarker
|
group |
BEFREE |
Our study indicates for the first time that, in addition to its role in brain development, MCPH1 also functions as a tumor suppressor gene and is regulated by miR-27a.
|
23472065 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Direct intratumoral injection of miR-27a* inhibited tumor growth in vivo.
|
23963114 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Taken together, this study has revealed miR-27a as a tumor suppressor and has identified SGPP1 and Smad2 as novel targets of miR-27a, linking to STAT3 for regulating cancer cell proliferation, apoptosis and migration in colorectal cancer.
|
25166914 |
2014 |
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 |