Malignant neoplasm of breast
|
0.360 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
Chest Pain
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Coughing
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Nausea and vomiting
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Esophageal carcinoma
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Lymphadenopathy
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Feeding difficulties in infancy
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Abnormality of the voice
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Clinodactyly of the 5th toe
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
DLC-1 may be a tumor suppressor gene in liver cancer as well as in other cancers.
|
9605766 |
1998 |
Adult Liver Carcinoma
|
0.070 |
Biomarker
|
disease |
BEFREE |
DLC-1 may be a tumor suppressor gene in liver cancer as well as in other cancers.
|
9605766 |
1998 |
Liver and Intrahepatic Biliary Tract Carcinoma
|
0.070 |
Biomarker
|
disease |
BEFREE |
DLC-1 may be a tumor suppressor gene in liver cancer as well as in other cancers.
|
9605766 |
1998 |
Malignant neoplasm of liver
|
0.070 |
Biomarker
|
disease |
BEFREE |
DLC-1 may be a tumor suppressor gene in liver cancer as well as in other cancers.
|
9605766 |
1998 |
Squamous cell carcinoma of esophagus
|
0.300 |
GeneticVariation
|
disease |
ORPHANET |
Molecular cloning of a candidate tumor suppressor gene, DLC1, from chromosome 3p21.3.
|
10213508 |
1999 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Transfection of DLC-1 into 5 HCC cell lines (two with DLC-1 deletion and three with intact DLC-1) showed significant growth inhibition in these two HCC cell lines with deleted DLC-1 with both 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and colony formation assays but not in three other HCC cell lines with intact DLC-1.
|
11118037 |
2000 |
Adult Liver Carcinoma
|
0.070 |
GeneticVariation
|
disease |
BEFREE |
We investigated the expression and deletion of DLC-1 (frequently deleted in liver cancer gene), first reported in 1998 and having a high homology with rat p122RhoGAP in hepatocellular carcinoma (HCC).
|
11118037 |
2000 |
Liver and Intrahepatic Biliary Tract Carcinoma
|
0.070 |
GeneticVariation
|
disease |
BEFREE |
We investigated the expression and deletion of DLC-1 (frequently deleted in liver cancer gene), first reported in 1998 and having a high homology with rat p122RhoGAP in hepatocellular carcinoma (HCC).
|
11118037 |
2000 |
Malignant neoplasm of liver
|
0.070 |
GeneticVariation
|
disease |
BEFREE |
We investigated the expression and deletion of DLC-1 (frequently deleted in liver cancer gene), first reported in 1998 and having a high homology with rat p122RhoGAP in hepatocellular carcinoma (HCC).
|
11118037 |
2000 |
Hepatocarcinogenesis
|
0.050 |
Biomarker
|
disease |
BEFREE |
Our findings suggest that DLC-1 may play an important role in hepatocarcinogenesis.
|
11118037 |
2000 |
Liver neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
DLC-1 is deleted in primary hepatocellular carcinoma and exerts inhibitory effects on the proliferation of hepatoma cell lines with deleted DLC-1.
|
11118037 |
2000 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
DLC-1 (deleted in liver cancer 1) is a candidate tumor suppressor gene for hepatocellular carcinoma and other cancers.
|
12034501 |
2002 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
DLC-1 (deleted in liver cancer 1) is a candidate tumor suppressor gene for hepatocellular carcinoma and other cancers.
|
12034501 |
2002 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
BEFREE |
Our results indicate a role of DLC-1 in BC carcinogenesis.
|
12759748 |
2003 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
BEFREE |
Furthermore, introduction of the DLC-1 cDNA abolished the in vivo tumorigenicity in nude mice, suggesting that the DLC-1 gene plays a role in breast cancer by acting as a bona fide tumor suppressor gene.
|
12545165 |
2003 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
While the pathogenic relevance of the intronic polymorphism is not known, the low rate of mutation of the DLC-1 gene in HCC implies that genomic deletion and promoter methylation primarily account for the altered expression and tumor suppressive inactivation of the DLC-1 gene.
|
12792785 |
2003 |