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BRMS1 reduces the metastatic potential, but not the tumorogenicity, of human breast cancer and melanoma cell lines. Additionally we are shipping BRMS1 Antibodies (64) and BRMS1 Kits (4) and many more products for this protein.
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BRMS1 promoter methylation and aberrant protein expression seem to be related to high-risk types of human papilloma virus-induced carcinogenesis in uterine cervix.
miR (show MLXIP Proteins)-346 promotes migration and invasion of nasopharyngeal carcinoma cells via targeting BRMS1.
expression of BRMS1 and/or HPA (show HPSE Proteins) might be closely related to the carcinogenesis, clinical biological behaviors, and prognosis of gallbladder adenocarcinoma
A novel link has been discussed between CDK2 (show CDK2 Proteins) expression and cell migration by characterizing the CDK2 (show CDK2 Proteins)-mediated phosphorylation of BRMS1.
Phosphorylation of BRMS1 by CDK2 (show CDK2 Proteins) regulates the migration of tumor cells.
Data show that Cullin3 exerts its function through promoting breast-cancer metastasis suppressor 1 (BRMS1) protein degradation, which was associated with epithelial-mesenchymal transition (EMT (show ITK Proteins)), migration and invasion.
The studies reviewed here with respect to BRMS1 structure, cellular effects, intracellular signaling, and clinical value consolidate the importance of BRMS1 in the development of metastasis.
Aberrant methylation of BRMS1 frequently occurs in the down-regulation of BRMS1 in triple negative breast cancer and that it may play a role in the metastasis of breast cancer.
the present study demonstrates a mechanical cascade of BRMS1 suppressing cancer cell invasion through downregulating HIF-1alpha (show HIF1A Proteins) transcript and consequently reducing Snail (show SNAI1 Proteins) and TWIST1 (show TWIST1 Proteins) expression.
MRTF-A and STAT3 (show STAT3 Proteins) synergistically recruited DNMT1 (show DNMT1 Proteins) to hypermethylate the promoter of BRMS1 and affect the expression of BRMS1.MRTF-A and STAT3 (show STAT3 Proteins) promote breast cancer cell migration via hypermethylating BRSM1.
findings indicate the expression of Brms1L (show BRMS1L Proteins) depends on beta-catenin (show CTNNB1 Proteins) activity and contributes to follicle stimulating hormone beta (show FSHB Proteins) induction by Gonadotropin-Releasing Hormone.
The Brms1 suppressed pulmonary metastasis and promoted apoptosis of tumor cells located in the lungs but not in the mammary glands.
BRMS1 may participate in transcriptional regulation via interaction with the mSin3.HDAC (show HDAC3 Proteins) complex
results show for the first time that BRMS1 contains both nuclear import and export signals enabling its nucleo-cytoplasmic shuttling
This gene reduces the metastatic potential, but not the tumorogenicity, of human breast cancer and melanoma cell lines. The protein encoded by this gene localizes primarily to the nucleus and is a component of the mSin3a family of histone deacetylase complexes (HDAC). The protein contains two coiled-coil motifs and several imperfect leucine zipper motifs. Alternative splicing results in two transcript variants encoding different isoforms.
breast cancer metastasis suppressor 1
, breast cancer metastasis-suppressor 1
, breast cancer metastasis-suppressor 1 homolog
, breast cancer metastasis-suppressor 1-like protein