Absent nasal septal cartilage
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Adenocarcinoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Moreover, SIX3 mRNA expression was associated with significantly improved overall survival (OS) and progression-free survival (PFS) in adenocarcinoma patients and patients with bronchioloalveolar carcinoma (BAC) features.
|
23977152 |
2013 |
Adenocarcinoma of lung (disorder)
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Association of SIX3 expression levels with clinical outcomes of patients with lung adenocarcinoma was evaluated using the Kaplan-Meier method and a multivariate Cox proportional hazards regression model.
|
23977152 |
2013 |
Adrenal hypoplasia
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Adult Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Epigenetically controlled Six3 expression regulates glioblastoma cell proliferation and invasion alongside modulating the activation levels of WNT pathway members.
|
28643150 |
2017 |
Agenesis of corpus callosum
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Alobar Holoprosencephaly
|
0.500 |
Biomarker
|
disease |
CTD_human |
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
|
10369266 |
1999 |
Alobar Holoprosencephaly
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
Ambiguous Genitalia
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Anterior pituitary agenesis
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Anteverted nostril
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Arhinencephaly
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
|
10369266 |
1999 |
Arrhinia
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Asthma
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Astrocytoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Importantly, interactions between AURKA and AURKB stabilize and protect AURKA/B from degradation, and overexpression of SIX3 does not affect these interactions; SIX3 also acts as a tumor suppressor, and it increases p53 activity and expression at the post-translational level by the negative regulation of AURKA or AURKB, reduces the events of numerical centrosomal aberrations and misaligned chromosomes, and significantly inhibits the proliferation, invasion, and tumorigenesis of astrocytoma in vitro and in vivo.
|
28595628 |
2017 |
Bifid uvula
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Breast Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
However, high SIX3 mRNA level was a protective factor for OS and RFS of basal-like breast cancer patients.Our study suggested that members of SIX family played distinct roles in breast cancer.
|
27399099 |
2016 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
We demonstrate that the SIX3/LSD1/NuRD(MTA3) complex inhibits carcinogenesis in breast cancer cells and suppresses metastasis in breast cancer.
|
29463994 |
2018 |
Bronchioloalveolar Adenocarcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Moreover, SIX3 mRNA expression was associated with significantly improved overall survival (OS) and progression-free survival (PFS) in adenocarcinoma patients and patients with bronchioloalveolar carcinoma (BAC) features.
|
23977152 |
2013 |
Carcinogenesis
|
0.050 |
Biomarker
|
phenotype |
BEFREE |
Little is known about the role of SIX3 in human tumorigenesis.
|
23977152 |
2013 |
Carcinogenesis
|
0.050 |
Biomarker
|
phenotype |
BEFREE |
However, studies on the function of SIX3 in human tumorigenesis remain rare.
|
30672777 |
2019 |
Carcinogenesis
|
0.050 |
Biomarker
|
phenotype |
BEFREE |
However, little is known about the role of Six3 in human tumorigenesis.
|
28643150 |
2017 |
Carcinogenesis
|
0.050 |
Biomarker
|
phenotype |
BEFREE |
We demonstrate that the SIX3/LSD1/NuRD(MTA3) complex inhibits carcinogenesis in breast cancer cells and suppresses metastasis in breast cancer.
|
29463994 |
2018 |
Carcinogenesis
|
0.050 |
AlteredExpression
|
phenotype |
BEFREE |
Importantly, interactions between AURKA and AURKB stabilize and protect AURKA/B from degradation, and overexpression of SIX3 does not affect these interactions; SIX3 also acts as a tumor suppressor, and it increases p53 activity and expression at the post-translational level by the negative regulation of AURKA or AURKB, reduces the events of numerical centrosomal aberrations and misaligned chromosomes, and significantly inhibits the proliferation, invasion, and tumorigenesis of astrocytoma in vitro and in vivo.
|
28595628 |
2017 |
Carcinoma of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
Wound healing assays were used to assess cell migration, and microarrays were utilized to examine genes regulated by SIX3 in lung cancer cells.
|
23977152 |
2013 |