Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
<i>TP53, KRAS, APC</i>) has limited diagnostic sensitivity (40-60%), however, methylated DNA including <i>SEPT9, SFRP1, SDC2</i> can be applied with higher sensitivity (up to 90%) for CRC.Circulating miRNAs (e.g. miR-21, miR-92, miR-141) provide comparably high sensitivity for CRC as the circulating tumor cell mRNA markers (e.g.EGFR, CK19, CK20, CEA).
|
31046485 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Methylated SEPT9 is a novel circulating tumor DNA marker for colorectal cancer, while the effects of various colorectal cancer clinicopathological factors on its detection performance have not been fully evaluated.
|
30223720 |
2018 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
Pre-therapeutic levels of SHOX2 and SEPT9 ccfDNA methylation were strongly associated with Union for International Cancer Control (UICC) stages, tumour (T), nodal (N), and metastasis (M) categories, and histological grade (all P ≤ 0.001), as well as lymphatic invasion and extracapsular lymph node extension (all P< 0.05).
|
29610456 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Repression of Septin9 and Septin2 suppresses tumor growth of human glioblastoma cells.
|
29724999 |
2018 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
The SEPT9 gene is a key regulator of cell division and tumor suppressor whose hypermethylation is associated with liver carcinogenesis.
|
29627389 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The mean levels of plasma septin-9 in epithelial ovarian carcinoma patients with tumor family history or distant metastases were significantly higher than that of patients without (P = 0.040, P = 0.025).
|
29970704 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
A three-gene panel (MGMT, RASSF1A, SEPT9) identified malignancy with 96.6% sensitivity, 74.0% specificity and 91.5 positive predictive value (area under the curve: 0.97), independently of tumor location, stage, and molecular pathway.
|
29486770 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We confirmed that HOXB2 and SEPT9 were highly methylated in LNM-positive tumors in 59 ESCC validation samples.
|
28465481 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In the present study, we analyze the protein expression of Sept9_i2, an uncharacterized isoform, in breast cancer cell lines and tumors and describe its specific impact on cancer cell migration and Sept9 cytoskeletal distribution.
|
28338090 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Methylation of the SEPT9_v2 promoter as a novel marker for the detection of circulating tumor DNA in breast cancer patients.
|
27499429 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
This comprehensive analysis of SEPT9 provides substantial evidence for increased SEPT9 expression as a consequence of genomic amplification and is the first study to profile SEPT9_v1 through SEPT9_v7 isoform-specific mRNA expression in tumor and nontumor tissues from patients with breast cancer.
|
24127542 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SEPT9 plays a role in multiple cancers as either an oncogene or a tumor suppressor gene.
|
23988185 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SEPT9_i1-HIF-1 activation promotes tumor growth and angiogenesis.
|
20407014 |
2010 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Small interfering RNA-mediated and short hairpin RNA-mediated inhibition of SEPT9_v1 expression in two BCCs with high levels of endogenous SEPT9_v1 expression inhibited neoplastic growth properties of the cells.
|
17875694 |
2007 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We now describe a comprehensive analysis of SEPT9 expression specifically in serous and mucinous ovarian tumours (benign, borderline and malignant), using cDNA microarray, semi- and quantitative RTPCR of microdissected archival tumour material.
|
16161048 |
2006 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
We have studied the expression of wild-type- and GTP-binding mutants (G144V and S148N) of the SEPT9_v4 isoform in the MCF7 cell line as a model for its deregulation in neoplasia.
|
15902694 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Our data indicate that the overexpression of SEPT9 in neoplasia is not simply a proliferation-associated phenomenon, despite its role in cytokinesis.
|
15782116 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We identified down-regulation of Thsp1- and Bax-regulated apoptotic response in those tumors with Sept9 overexpression, an effect that could be reversed by inhibiting Sept9 expression using transfection with small interference RNA.
|
12727837 |
2003 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
A genomic fragment was used as a hybridization probe to isolate a 3-kb cDNA clone, the expression of which was upregulated in one of two tumors harboring a provirus in Sint1.
|
10666245 |
2000 |