Acute lymphocytic leukemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
To verify a linkage between c-myb and NmU, their mRNA levels were quantitated using real-time polymerase chain reaction in primary acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL), as well as normal hematopoietic cells.
|
15187020 |
2004 |
Leukemia, Myelocytic, Acute
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
To verify a linkage between c-myb and NmU, their mRNA levels were quantitated using real-time polymerase chain reaction in primary acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL), as well as normal hematopoietic cells.
|
15187020 |
2004 |
Myeloid Leukemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Neuromedin U: a Myb-regulated autocrine growth factor for human myeloid leukemias.
|
15187020 |
2004 |
Myeloid Leukemia
|
0.010 |
AlteredExpression
|
disease |
LHGDN |
Combined, these results suggest that NmU expression is related to Myb and that the NmU/NMU1R axis constitutes a previously unknown growth-promoting autocrine loop in myeloid leukemia cells.
|
15187020 |
2004 |
Precursor Cell Lymphoblastic Leukemia Lymphoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
To verify a linkage between c-myb and NmU, their mRNA levels were quantitated using real-time polymerase chain reaction in primary acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL), as well as normal hematopoietic cells.
|
15187020 |
2004 |
Squamous cell carcinoma of the head and neck
|
0.020 |
Biomarker
|
disease |
BEFREE |
We identified 12 novel methylated genes in HNSCC cell lines, including PGP9.5, cyclin A1, G0S2, bone-morphogenetic protein 2A, MT1G, and neuromedin U, which showed frequent promoter hypermethylation in primary HNSCC (60%, 45%, 35%, 25%, 25%, and 20%, respectively).
|
15342377 |
2004 |
Obesity
|
0.250 |
GeneticVariation
|
disease |
BEFREE |
Studies of the neuromedin U-2 receptor gene in human obesity: evidence for the existence of two ancestral forms of the receptor.
|
15525579 |
2004 |
Malignant neoplasm of breast
|
0.050 |
AlteredExpression
|
disease |
BEFREE |
The gene expression profiles of the NMU-induced primary tumors were most similar to ER-positive, low to intermediate grade breast cancer.
|
15845649 |
2005 |
Breast Carcinoma
|
0.050 |
AlteredExpression
|
disease |
BEFREE |
The gene expression profiles of the NMU-induced primary tumors were most similar to ER-positive, low to intermediate grade breast cancer.
|
15845649 |
2005 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
The NMU breast cancer model induced in the rat is used for the study of mammary carcinogenesis because it closely mimics human breast disease.
|
15845649 |
2005 |
Breast Diseases
|
0.010 |
Biomarker
|
group |
BEFREE |
The NMU breast cancer model induced in the rat is used for the study of mammary carcinogenesis because it closely mimics human breast disease.
|
15845649 |
2005 |
Obesity
|
0.250 |
Biomarker
|
disease |
BEFREE |
Screening of neuromedin U2 receptor (NMU2R) ligands may be very useful to treat obesity for the reason that centrally administered neuromedin U affects feeding behavior, energy expenditure, and pituitary.
|
16111886 |
2005 |
Malignant Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
In conclusion, NMU is a RhoGDI2-regulated gene that appears important for tumorigenicity, lung metastasis and cancer cachexia, and thus a promising therapeutic target in cancer.
|
16878152 |
2007 |
Neoplasm Metastasis
|
0.060 |
AlteredExpression
|
phenotype |
LHGDN |
Recently, we noted an inverse correlation between tumor RhoGDI2 and Neuromedin U (NMU) expression, suggesting that NMU might be a target of the lung metastasis suppressor effect of RhoGDI2.
|
16878152 |
2007 |
Neoplasm Metastasis
|
0.060 |
Biomarker
|
phenotype |
BEFREE |
Neuromedin U is regulated by the metastasis suppressor RhoGDI2 and is a novel promoter of tumor formation, lung metastasis and cancer cachexia.
|
16878152 |
2007 |
Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
Furthermore, NMU-overexpressing xenografts were associated with lower animal body weight than control tumors, indicating a possible role of NMU in cancer cachexia.
|
16878152 |
2007 |
Primary malignant neoplasm
|
0.050 |
Biomarker
|
group |
BEFREE |
In conclusion, NMU is a RhoGDI2-regulated gene that appears important for tumorigenicity, lung metastasis and cancer cachexia, and thus a promising therapeutic target in cancer.
|
16878152 |
2007 |
Tumor Progression
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Here we evaluated whether NMU is regulated by RhoGDI2 and is functionally important in tumor progression.
|
16878152 |
2007 |
Malignant neoplasm of urinary bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We used small interfering RNA knockdown of endogenous RhoGDI2 in poorly tumorigenic and non-metastatic human bladder cancer T24 cells and observed increased NMU RNA expression.
|
16878152 |
2007 |
Bladder Neoplasm
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We used small interfering RNA knockdown of endogenous RhoGDI2 in poorly tumorigenic and non-metastatic human bladder cancer T24 cells and observed increased NMU RNA expression.
|
16878152 |
2007 |
Bladder Neoplasm
|
0.010 |
AlteredExpression
|
disease |
LHGDN |
Although NMU overexpression did not increase the monolayer growth of T24 or related T24T poorly metastatic human bladder cancer cells, it did augment anchorage-independent growth for the latter.
|
16878152 |
2007 |
Cachexia
|
0.010 |
AlteredExpression
|
phenotype |
LHGDN |
Neuromedin U is regulated by the metastasis suppressor RhoGDI2 and is a novel promoter of tumor formation, lung metastasis and cancer cachexia.
|
16878152 |
2007 |
Secondary malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Recently, we noted an inverse correlation between tumor RhoGDI2 and Neuromedin U (NMU) expression, suggesting that NMU might be a target of the lung metastasis suppressor effect of RhoGDI2.
|
16878152 |
2007 |
Carcinoma of bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We used small interfering RNA knockdown of endogenous RhoGDI2 in poorly tumorigenic and non-metastatic human bladder cancer T24 cells and observed increased NMU RNA expression.
|
16878152 |
2007 |
Cancer cachexia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Furthermore, NMU-overexpressing xenografts were associated with lower animal body weight than control tumors, indicating a possible role of NMU in cancer cachexia.
|
16878152 |
2007 |