Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Like certain other sirtuins, SIRT6 isemerging to have an oncogenic function as well as tumor suppressor roles in cancer.
|
31696978 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Sirtuin 6 (SIRT6), a tumor suppressor, modulates aerobic glycolysis of malignant cells and has an impact on tumorigenesis.
|
30989475 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Sirtuin (SIRT)6 is a member of the sirtuin family, which may be useful targets in the treatment of tumors.
|
31257493 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, the effect of NQO1 and SIRT6 on tumor growth was determined in cell model and orthotopic tumor implantation model.
|
31842909 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We generated shSIRT6 LoVo cells and xenograft mouse to reveal the essential role of SIRT6 in cell apoptosis and tumor growth.
|
31149050 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
This review focuses on one the mammalian sirtuins, SIRT6, which has emerged as an important regulator of longevity and appears to have multiple biochemical functions that interfere with tumor development and may be useful in cancer prevention and for site-specific treatment.
|
31591350 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The present study suggested that SIRT6 may serve as a tumor suppressor during the development of osteosarcoma.
|
30655890 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Sirt family has been reported playing a significant role in the cancer development, especial its deacetylase activity plays a key function, but whether SIRT6 plays a role in mediating tumor epithelial-mesenchymal transition (EMT) and metastasis in colon cancer has not been explored.
|
29227545 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Thus, we conclude that, by targeting SIRT6, miR-125b can function as a tumor suppressor to induce the cellular senescence and apoptosis in hepatocellular carcinogenesis and could provide a novel insight for HCC treatment.
|
30034937 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The reduced expression of SIRT6 and increased expression of NMNAT2 were associated with the tumor depth invasion, stage, differentiation grade (SIRT6 only) and the presence of lymph node metastasis (P<0.05).
|
30333863 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, the present study confirms that SIRT6 functions as a tumor suppressor gene in colon cancer by modulating PTEN/AKT signaling, which may provide a novel target for the treatment of colon cancer.
|
29957460 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Overall, our findings show how the tumor suppressor SIRT6 is regulated in hepatocellular carcinoma and establish the mechanism underlying UBE3A-mediated tumorigenesis in this disease.<b>Significance:</b> These findings provide mechanistic insights into regulation of the tumor suppressive sirtuin SIRT6 and its implications for the development of hepatocellular carcinoma.<i></i>.
|
29217762 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Silent information regulator 6 (SIRT6) is broadly considered as a tumor suppressor due to its function in the suppression of oncogene expression.
|
29552180 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Bioinformatic predictions, a luciferase reporter assay, and protein expression analysis suggested that miR-186 could inhibit the protein levels of SIRT6, a purported tumor suppressor gene.
|
29125477 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SIRT6 study has concentrated on the effects of this molecule on tumors and shown promising trends in understanding neural diseases.
|
30457131 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Our results provide preliminary evidence suggesting that SIRT1, SIRT3, and SIRT6 function as tumor suppressors in RCC.
|
28935184 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Decreased SIRT6 expression was associated with unfavorable clinical parameters including tumor differentiation, tumor size and TNM stage.
|
28656307 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our data identify SIRT6 as a putative molecular target that hinders stemness of tumors with PI3K activation.
|
28228253 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our study establishes lysine fatty acylation as a previously unknown mechanism that regulates the Ras family of GTPases and provides an important mechanism by which SIRT6 functions as a tumor suppressor.
|
28406396 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Sirtuin 6, a member of sirtuin family, is generally regarded as a tumor suppressor as it participates in suppressing hypoxia-inducible factor 1α and MYC transcription activity by deacetylating H3K9 (histone H3 lysine 9) and H3K56 (histone H3 lysine) at promoters of target genes, leading to the aerobic glycolysis inhibition and cell growth suppression.
|
28653878 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Sirt6 has been shown as a tumor suppressor partially via inhibiting the expression of c-Myc target genes and ribosome biogenesis.
|
26898756 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Sirt6 acts as a tumor suppressor and deficiency of Sirt6 leads to cardiac hypertrophy and heart failure.
|
27045575 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SIRT6 has recently been reported to be a tumor suppressor that controls cancer metabolism, although this effect of SIRT6 is still in dispute.
|
26648570 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
SIRT6 expression was frequently upregulated in clinical HCC samples, and its expression was highly associated with tumor grade (P = 0.02), tumor size (P = 0.02), vascular invasion (P = 0.004), and shorter survival (P = 0.024).
|
26861461 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results revealed that SIRT6 might function as a tumor suppressor of endometrial cancer cells.
|
26183563 |
2015 |