Sezary Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
Within the first region of deletion at 10q23.33-10q24.1, around microsatellite marker D10S185 (2.77 Mb), 23 genes were identified, including three (KIF11, HHEX, and HELLS) with functions that, if dysregulated, could be critical in MF and SS.
|
15540164 |
2005 |
Malignant neoplasm of stomach
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
TP53 in gastric cancer: mutations in the l3 loop and LSH motif DNA-binding domains of TP53 predict poor outcome.
|
15254976 |
2004 |
Stomach Carcinoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
TP53 in gastric cancer: mutations in the l3 loop and LSH motif DNA-binding domains of TP53 predict poor outcome.
|
15254976 |
2004 |
Tumor Cell Invasion
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Moreover, specific mutations in functional domain (L3 and LSH), together with advanced TNM stage, node involvement, depth of invasion, diffuse histotype, proved to be significantly related to quicker relapse and to shorter overall survival.
|
15254976 |
2004 |
Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, targeting HELLS may permit the functional disruption of the relatively undruggable MYC and E2F3 transcription factors and serve as a novel therapeutic paradigm for glioblastoma.
|
30779712 |
2019 |
Glioma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
The potential clinical significance of HELLS was reinforced by improved survival of tumor-bearing mice upon targeting HELLS and poor prognosis of glioma patients with elevated HELLS expression.
|
30779712 |
2019 |
Neoplasm Metastasis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
In contrast, depletion of HELLS reduced HCC growth and metastasis both in vitro and in vivo.
|
30516846 |
2019 |
Adult Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, targeting HELLS may permit the functional disruption of the relatively undruggable MYC and E2F3 transcription factors and serve as a novel therapeutic paradigm for glioblastoma.
|
30779712 |
2019 |
Childhood Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, targeting HELLS may permit the functional disruption of the relatively undruggable MYC and E2F3 transcription factors and serve as a novel therapeutic paradigm for glioblastoma.
|
30779712 |
2019 |
Glioblastoma Multiforme
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, targeting HELLS may permit the functional disruption of the relatively undruggable MYC and E2F3 transcription factors and serve as a novel therapeutic paradigm for glioblastoma.
|
30779712 |
2019 |
Liver carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
In contrast, depletion of HELLS reduced HCC growth and metastasis both in vitro and in vivo.
|
30516846 |
2019 |
Liver carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Therefore, LSH may be a novel predictor for prognosis and a potential therapeutic target for HCC.
|
31066149 |
2019 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
This suggests that while HELLS may serve as a biomarker for tumorigenesis and for RB-E2F pathway status, it is unlikely to serve as a relevant target for therapeutics in osteosarcoma.
|
30220967 |
2018 |
Glioblastoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Up-regulation of transcription factor E2F1 in astrocytomas and glioblastoma was associated with the progression of gliomas and correlated with LSH expression.
|
28042322 |
2017 |
Glioma
|
0.020 |
Biomarker
|
disease |
BEFREE |
A mechanistic link between LSH expression and activation of the LPR6/ GSK3β/E2F1 axis in gliomas illustrates a novel role of LSH in malignant astrocytomas and glioblastoma.
|
28042322 |
2017 |
Neoplasm Metastasis
|
0.020 |
GeneticVariation
|
phenotype |
BEFREE |
Decrease in Lymphoid Specific Helicase and 5-hydroxymethylcytosine Is Associated with Metastasis and Genome Instability.
|
29109788 |
2017 |
Adult Glioblastoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Up-regulation of transcription factor E2F1 in astrocytomas and glioblastoma was associated with the progression of gliomas and correlated with LSH expression.
|
28042322 |
2017 |
Childhood Glioblastoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Up-regulation of transcription factor E2F1 in astrocytomas and glioblastoma was associated with the progression of gliomas and correlated with LSH expression.
|
28042322 |
2017 |
Glioblastoma Multiforme
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Up-regulation of transcription factor E2F1 in astrocytomas and glioblastoma was associated with the progression of gliomas and correlated with LSH expression.
|
28042322 |
2017 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Linking expression of FOXM1, CEP55 and HELLS to tumorigenesis in oropharyngeal squamous cell carcinoma.
|
22109759 |
2011 |
Non-Small Cell Lung Carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
The expression of chromatin modifier lymphoid-specific helicase (LSH) and GINS4 was assessed in tumor and normal tissue from 79 patients with NSCLC with clinical characteristics.
|
31253190 |
2019 |
Tumor Progression
|
0.030 |
PosttranslationalModification
|
phenotype |
BEFREE |
The chromatin modifier lymphoid-specific helicase (LSH) is essential for DNA methylation and cancer progression as a transcriptional repressor.
|
31594538 |
2019 |
Malignant neoplasm of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
GINS4 facilitates lung cancer progression by promoting key characteristics of tumor potential, and LSH epigenetically interacts with and stabilizes GINS4 transcripts.
|
31253190 |
2019 |
Carcinoma of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
GINS4 facilitates lung cancer progression by promoting key characteristics of tumor potential, and LSH epigenetically interacts with and stabilizes GINS4 transcripts.
|
31253190 |
2019 |
Primary malignant neoplasm of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
GINS4 facilitates lung cancer progression by promoting key characteristics of tumor potential, and LSH epigenetically interacts with and stabilizes GINS4 transcripts.
|
31253190 |
2019 |