Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, although much is still unknown, Gpr49 may be critically involved in the development of HCCs with beta-catenin mutations and has the potential to be a new therapeutic target in the treatment of HCC.
|
12601349 |
2003 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
In conclusion, although much is still unknown, Gpr49 may be critically involved in the development of HCCs with beta-catenin mutations and has the potential to be a new therapeutic target in the treatment of HCC.
|
12601349 |
2003 |
Ankyloglossia
|
0.230 |
Biomarker
|
disease |
MGD |
Neonatal lethality of LGR5 null mice is associated with ankyloglossia and gastrointestinal distension.
|
15509778 |
2004 |
Ankyloglossia
|
0.230 |
Biomarker
|
disease |
BEFREE |
Neonatal lethality of LGR5 null mice is associated with ankyloglossia and gastrointestinal distension.
|
15509778 |
2004 |
Hepatocellular Adenoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Quantitative RT-PCR showed that FABP1 (liver fatty acid binding protein) and UGT2B7 were downregulated in HNF1alpha-inactivated HCA (P <or= 0.0002); GLUL (glutamine synthetase) and GPR49 overexpression were associated with beta-catenin-activating mutations (P <or= 0.0005), and SAA2 (serum amyloid A2) and CRP (C-reactive protein) were upregulated in inflammatory HCA (P = 0.0001).
|
17663417 |
2007 |
Colonic Neoplasms
|
0.350 |
Biomarker
|
group |
LHGDN |
Identification of stem cells in small intestine and colon by marker gene Lgr5.
|
17934449 |
2007 |
Basal cell carcinoma
|
0.010 |
AlteredExpression
|
disease |
LHGDN |
G-protein-coupled receptor GPR49 is up-regulated in basal cell carcinoma and promotes cell proliferation and tumor formation.
|
18688030 |
2008 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.040 |
Biomarker
|
disease |
BEFREE |
We performed an association study of 9 SNPs in or around JAZF1, CDC123/ CAMK1D, NOTCH2, BCL11A, ADAMTS9, VEGFA, DCD, THADA, and TSPAN8/ LGR5 with T2D and related quantitative traits (fasting insulin and glucose, indices derived from OGTT) in the isolated population of Sorbs (205 cases and 695 controls) and in a mixed German population (Leipzig) (938 subjects with and 918 without T2D).
|
19670153 |
2010 |
Ankyloglossia
|
0.230 |
GeneticVariation
|
disease |
BEFREE |
The aim of the present study was to characterize the phenotype and to verify sequence variations in the LGR5 gene in a Brazilian family with ankyloglossia associated with tooth number anomalies.
|
20042737 |
2010 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We prioritized three targets [centromere-associated protein E (Cenpe), Gpr49, and inosine monophosphate dehydrogenase type II] with previously determined roles in cancer.
|
20233875 |
2010 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
We prioritized three targets [centromere-associated protein E (Cenpe), Gpr49, and inosine monophosphate dehydrogenase type II] with previously determined roles in cancer.
|
20233875 |
2010 |
Malignant tumor of colon
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Moreover, LGR5 expression was higher in colon cancer cell lines derived from metastatic tumors compared with those from primary tumors.
|
20384634 |
2010 |
Colorectal Carcinoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
LGR5 expression showed marked variation among CRC cases and correlated significantly with lymphatic invasion, vascular invasion, tumor depth, lymph node metastasis, and tumor stage (IIIC vs. IIIB).
|
20384634 |
2010 |
Adenoma
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In clinical specimens, there was significant overexpression of LGR5 in 35 of 50 colorectal cancers (CRCs), and in seven of seven sporadic colonic adenomas, compared with matched normal mucosa.
|
20384634 |
2010 |
Malignant Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition to cancer cells, crypt base columnar cells of the small intestine and colon were shown by in situ hybridization to express LGR5.
|
20384634 |
2010 |
Neoplasm Metastasis
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Moreover, LGR5 expression was higher in colon cancer cell lines derived from metastatic tumors compared with those from primary tumors.
|
20384634 |
2010 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
LGR5 expression showed marked variation among CRC cases and correlated significantly with lymphatic invasion, vascular invasion, tumor depth, lymph node metastasis, and tumor stage (IIIC vs. IIIB).
|
20384634 |
2010 |
Carcinogenesis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
This is the first report suggesting the involvement of LGR5, not only in early events but also in late events in colorectal tumorigenesis.
|
20384634 |
2010 |
Colon Carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Moreover, LGR5 expression was higher in colon cancer cell lines derived from metastatic tumors compared with those from primary tumors.
|
20384634 |
2010 |
Tumor Cell Invasion
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
LGR5 expression showed marked variation among CRC cases and correlated significantly with lymphatic invasion, vascular invasion, tumor depth, lymph node metastasis, and tumor stage (IIIC vs. IIIB).
|
20384634 |
2010 |
Primary malignant neoplasm
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition to cancer cells, crypt base columnar cells of the small intestine and colon were shown by in situ hybridization to express LGR5.
|
20384634 |
2010 |
Malignant neoplasm of colon and/or rectum
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Overexpression of leucine-rich repeat-containing G protein-coupled receptor 5 in colorectal cancer.
|
20384634 |
2010 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
This large population-based study and meta-analysis further confirmed the modest effects of the JAZF1, TSPAN8/LGR5 and HHEX-IDE loci on type 2 diabetes in Chinese and other East Asians.
|
20927120 |
2010 |
Colorectal Carcinoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
This study supports a significant role for LGR5 in the CSC hypothesis in CRC: (1) Lgr5(+ve) CSCs, presumably derived from normal stem cells in colonic crypts, proliferate, and the gene is overexpressed during CRC development; (2) LGR5 expression is associated with activation of Wnt pathway, including oncogenic c-MYC and high energy production via glutaminolysis; (3) LGR5 expression may be a poor prognostic factor for CRC patients.
|
21125339 |
2011 |
Malignant Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
High level of LGR5 expression was associated with poor prognosis for CRC cancer patients (disease-free survival; p < 0.05).
|
21125339 |
2011 |