Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
We found seven miRNAs that significantly downregulated CHD5 expression in NB: miR-211, 17, -93, -20b, -106b, -204, and -3666.
|
26895110 |
2016 |
Neuroblastoma
|
0.400 |
Biomarker
|
disease |
CTD_human |
Recurrent alterations at relapse included mutations in the putative CHD5 neuroblastoma tumor suppressor, chromosome 9p losses, DOCK8 mutations, inactivating mutations in PTPN14 and a relapse-specific activity pattern for the PTPN14 target YAP.
|
26121086 |
2015 |
Neuroblastoma
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Recurrent alterations at relapse included mutations in the putative CHD5 neuroblastoma tumor suppressor, chromosome 9p losses, DOCK8 mutations, inactivating mutations in PTPN14 and a relapse-specific activity pattern for the PTPN14 target YAP.
|
26121086 |
2015 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
We explored the role of CHD5 expression in the neuronal differentiation of NB cell lines.
|
26245651 |
2015 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, low CHD5 expression is strongly associated with unfavorable clinical and biologic features as well as outcome in neuroblastomas and many other tumor types.
|
24419087 |
2014 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Reintroduction of CHD5 into neuroblastoma cells represses WEE1 expression, demonstrating that CHD5 can function as a repressor in cells.
|
25247294 |
2014 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
These findings provide insights into the regulatory role of CHD5 during neurogenesis and suggest how inactivation of this candidate tumor suppressor might contribute to neuroblastoma.
|
23948251 |
2013 |
Neuroblastoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Unlike wild-type Chd5, Chd5-PHD mutants are unable to induce differentiation or efficiently suppress the growth of human neuroblastoma in vivo.
|
23318260 |
2013 |
Neuroblastoma
|
0.400 |
PosttranslationalModification
|
disease |
BEFREE |
We conclude that (i) somatically acquired CHD5 mutations are rare in primary NBs, so inactivation probably occurs by deletion and epigenetic silencing; (ii) CHD5 expression and promoter methylation are associated with MYCN amplification, suggesting a possible interaction between these 2 genes; and (iii) high CHD5 expression is strongly correlated with favorable clinical/biological features and outcome.
|
22294723 |
2012 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
In the present study, our results showed that genistein, an element found in soy, is an epigenetic modifier able to decrease hypermethylation levels of CHD5, and enhances the expression of CHD5 as well as p53, possibly contributing to inhibition of NB growth in vivo and tumor microvessel formation.
|
22960751 |
2012 |
Neuroblastoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Expression of the neuron-specific protein CHD5 is an independent marker of outcome in neuroblastoma.
|
20950435 |
2010 |
Neuroblastoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Among the best candidate genes predisposing to the development of neuroblastoma located in 1p36, the AJAP1 gene is the only gene present in the duplication while CHD5, TNFRSF25 and CAMTA1 are located outside of the rearrangement.
|
18672103 |
2009 |
Neuroblastoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Our mutation and expression analysis in neuroblastoma cell lines, combined with expression analysis in normal tissues, putative function and prior implication in neuroblastoma pathogenesis, suggests that the most promising TSG deleted from the 1p36 SRD is CHD5, but TNFRSF25, CAMTA1 and AJAP1 are also viable candidates.
|
17667943 |
2008 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
CHD5 expression was very low or absent in neuroblastoma cell lines.
|
18577749 |
2008 |
Neuroblastoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
We examined a panel of neuroblastoma cell lines for CHD5 expression, which was consistently low or undetectable in all these lines.
|
12592387 |
2003 |
Colorectal Carcinoma
|
0.340 |
PosttranslationalModification
|
disease |
BEFREE |
Thus, it can be concluded that the CHD5 methylation rate rises gradually in the evolution of CRC, which is related to the occurrence and development of CRC.
|
26753653 |
2016 |
Colorectal Carcinoma
|
0.340 |
PosttranslationalModification
|
disease |
BEFREE |
The epigenetic silencing mechanisms of CHD5 in colorectal cancer have not been well studied.
|
24243398 |
2014 |
Colorectal Carcinoma
|
0.340 |
AlteredExpression
|
disease |
BEFREE |
Our previous work revealed that the low expression of CHD5 in colorectal cancer is correlated with CHD5 promoter CpG island hypermethylation.
|
22235338 |
2012 |
Colorectal Carcinoma
|
0.340 |
Biomarker
|
disease |
CTD_human |
Genomic and epigenomic integration identifies a prognostic signature in colon cancer.
|
21278247 |
2011 |
Colorectal Carcinoma
|
0.340 |
PosttranslationalModification
|
disease |
BEFREE |
We investigated the status of CAN gene methylation and CHD5 protein expression in African American CRC tissue microarrays (TMA) using immunohistochemical staining.
|
19750230 |
2009 |
Malignant neoplasm of breast
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
CHD5 protein expression was also reduced in breast cancer, and lack of CHD5 expression significantly correlated with higher tumor stage, ER/PR-negativity, HER2 positivity, distant metastasis and worse patient survival (P ≤ 0.01).
|
22569290 |
2012 |
Malignant neoplasm of breast
|
0.320 |
GeneticVariation
|
disease |
BEFREE |
We analyzed all 41 coding exons of CHD5 for somatic mutations in 123 primary ovarian cancers as well as 60 primary breast cancers using high-resolution melt analysis.
|
18953434 |
2008 |
Malignant neoplasm of breast
|
0.320 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
Colorectal Neoplasms
|
0.300 |
Biomarker
|
group |
CTD_human |
Genomic and epigenomic integration identifies a prognostic signature in colon cancer.
|
21278247 |
2011 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
rs187960998 in miR-211 was highly associated with a decreased risk of CC in the Chinese population by deregulating a tumor suppressive gene CHD5.
|
30655677 |
2019 |