Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Collectively, our present results provide the first evidence that UbcH10 is highly expressed in various human primary tumors and that UbcH10 has an ability to promote cell growth and malignant transformation.
|
12874022 |
2003 |
Carcinogenesis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Intriguingly, UbcH10 was expressed at high levels in primary tumors derived from the lung, stomach, uterus, and bladder as compared with their corresponding normal tissues, suggesting that UbcH10 is involved in tumorigenesis or progression of the tumor.
|
12874022 |
2003 |
Malignant transformation
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Collectively, our present results provide the first evidence that UbcH10 is highly expressed in various human primary tumors and that UbcH10 has an ability to promote cell growth and malignant transformation.
|
12874022 |
2003 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
To evaluate whether inhibition of UbcH10 function may be therapeutically relevant in cancer, we used small interfering RNAs (siRNAs) to silence UbcH10 transcription selectively.
|
15208666 |
2004 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Together, these data demonstrate that UbcH10 plays an important role in tumor development and that its inhibition in combination with agonists of the TRAIL receptor may provide an enhanced therapeutic index.
|
15208666 |
2004 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
To evaluate whether inhibition of UbcH10 function may be therapeutically relevant in cancer, we used small interfering RNAs (siRNAs) to silence UbcH10 transcription selectively.
|
15208666 |
2004 |
Carcinoma
|
0.020 |
AlteredExpression
|
group |
BEFREE |
We also show that UbcH10 overexpression in gastro-esophageal, and probably other carcinomas may be a direct consequence of chromosomal amplification at the UbcH10 locus, 20q13.1, a region known to be amplified in diverse tumors.
|
15208666 |
2004 |
Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We show here that the ubiquitin conjugase, UbcH10, is significantly overexpressed in many different types of cancers and is associated with the degree of tumor differentiation in carcinomas of the breast, lung, ovary and bladder, as well as in glioblastomas.
|
15208666 |
2004 |
Thyroid carcinoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
The block of UbcH10 protein synthesis induced by RNA interference significantly reduced the growth rate of thyroid carcinoma cell lines.
|
16106252 |
2005 |
Anaplastic thyroid carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Immunohistochemical studies performed on paraffin-embedded tissue sections showed abundant UbcH10 levels in thyroid anaplastic carcinoma samples, whereas no detectable UbcH10 expression was observed in normal thyroid tissues, in adenomas and goiters.
|
16106252 |
2005 |
Adenoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Immunohistochemical studies performed on paraffin-embedded tissue sections showed abundant UbcH10 levels in thyroid anaplastic carcinoma samples, whereas no detectable UbcH10 expression was observed in normal thyroid tissues, in adenomas and goiters.
|
16106252 |
2005 |
Anaplastic carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Taken together, these results would indicate that UbcH10 overexpression is involved in thyroid cell proliferation, and may represent a marker of thyroid anaplastic carcinomas.
|
16106252 |
2005 |
myeloblastosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cyclin-dependent kinase inhibitor 2A (CDKN2A/p16), mesoderm-specific transcript, forkhead box M1, v-myb myeloblastosis viral oncogene homolog (avian)-like2 (v-Myb), minichromosome maintenance proteins 2, 4, and 5, cyclin B1, prostaglandin E synthase (PTGES), topoisomerase II alpha (TOP2A), ubiquitin-conjugating enzyme E2C, CD97 antigen, E2F transcription factor 1, and dUTP pyrophosphatase were among the most highly overexpressed genes in CVX when compared to NCK.
|
15629771 |
2005 |
Malignant neoplasm of breast
|
0.400 |
Biomarker
|
disease |
BEFREE |
Combination of multiple mRNA markers (PTTG1, Survivin, UbcH10 and TK1) in the diagnosis of Taiwanese patients with breast cancer by membrane array.
|
17220641 |
2006 |
Breast Carcinoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Combination of multiple mRNA markers (PTTG1, Survivin, UbcH10 and TK1) in the diagnosis of Taiwanese patients with breast cancer by membrane array.
|
17220641 |
2006 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tissue microarray showed elevated UBE2C in 70% (7 of 10) of dysplastic samples and in 87% (58 of 67) of tumors relative to metaplastic samples.
|
17217624 |
2006 |
Tumor Progression
|
0.060 |
GeneticVariation
|
phenotype |
BEFREE |
Our results showing aberrations in levels of gene expression and locus copy number of UBE2C suggest that this gene may play an important role in tumor progression leading to advanced colon cancer with liver metastasis.
|
16772118 |
2006 |
Neoplasm Metastasis
|
0.050 |
GeneticVariation
|
phenotype |
LHGDN |
Our results showing aberrations in levels of gene expression and locus copy number of UBE2C suggest that this gene may play an important role in tumor progression leading to advanced colon cancer with liver metastasis.
|
16772118 |
2006 |
Adenocarcinoma
|
0.030 |
Biomarker
|
group |
LHGDN |
Expression and effect of inhibition of the ubiquitin-conjugating enzyme E2C on esophageal adenocarcinoma.
|
17217624 |
2006 |
Colon Carcinoma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Our results showing aberrations in levels of gene expression and locus copy number of UBE2C suggest that this gene may play an important role in tumor progression leading to advanced colon cancer with liver metastasis.
|
16772118 |
2006 |
Barrett Esophagus
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Using oligonucleotide microarrays UBE2C expression was elevated in 73% (11 of 15) of EAs relative to Barrett's metaplasia.
|
17217624 |
2006 |
Malignant tumor of colon
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Our results showing aberrations in levels of gene expression and locus copy number of UBE2C suggest that this gene may play an important role in tumor progression leading to advanced colon cancer with liver metastasis.
|
16772118 |
2006 |
Colonic Neoplasms
|
0.010 |
GeneticVariation
|
group |
LHGDN |
Detection of aberrations of ubiquitin-conjugating enzyme E2C gene (UBE2C) in advanced colon cancer with liver metastases by DNA microarray and two-color FISH.
|
16772118 |
2006 |
Adenocarcinoma Of Esophagus
|
0.010 |
Biomarker
|
disease |
BEFREE |
EA-derived cells expressing UBE2C are sensitive to treatment with MG-262 and to silencing of UBE2C, suggesting that patients with EAs overexpressing UBE2C may benefit from agents targeting this ubiquitin-conjugating enzyme.
|
17217624 |
2006 |
Secondary malignant neoplasm of liver
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Our results showing aberrations in levels of gene expression and locus copy number of UBE2C suggest that this gene may play an important role in tumor progression leading to advanced colon cancer with liver metastasis.
|
16772118 |
2006 |