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May be related to cancer progression or tumor metastasis in a variety of organ sites, most likely through an interaction with the actin cytoskeleton.. Additionally we are shipping MTSS1 Antibodies (69) and many more products for this protein.
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Missing in metastasis B, regulated by DNMT1 (show DNMT1 Proteins), functions as a putative cancer suppressor in human lung giant-cell carcinoma.
Data identify MTSS1 as a new Akt2 (show AKT2 Proteins)-regulated gene, and point to suppression of MTSS1 as a key step in the metastasis-promoting effects of Akt2 (show AKT2 Proteins) in CRC (show CALR Proteins) cells.
Data suggest that overexpression of MAEL (show MAEL Proteins), caused by gene amplification and/or decreased miR (show MLXIP Proteins)-186, has a critical oncogenic role in UCB pathogenesis by downregulation of MTSS1.
Overexpression of MTSS1 in PDAC cell lines leads to a loss of migratory potential in vitro and an increase in overall survival in vivo. Data provide insight into an important role for MTSS1 in suppressing tumor cell invasion and migration driven by the tumor microenvironment.
Overexpression of MTSS1 reduced BUCC cell proliferation, cell-cycle progression and colony formation, but had no influence on BUCC cell apoptosis.
in contrast to MIM, which is a prototype of I-BAR proteins and does not contain an SH3 domain (show ITSN1 Proteins), IRTKS (show BAIAP2L1 Proteins) promoted serum-induced cell migration along with enhanced phosphorylation of mitogen activated kinases Erk1/2 and p38 (show CRK Proteins)
this study shows a previously unknown property of MIM that establishes the linkage of protein ubiquitylation with Rab (show HRB Proteins)-guided trafficking of CXCR4 (show CXCR4 Proteins) in endocytic vesicles
MTSS1 suppressed H1299 cell migration and invasion, and its expression level can be used as a new independent factor for determining the prognosis of non-small cell lung cancer.
MTSS1 is a new authentic target of miR (show MLXIP Proteins)-96 in prostate carcinoma.
Down-regulation of MTSS1 expression is associated with lymph node metastasis in Pancreatic Cancer.
Mtss1 is a key linker between the actin cytoskeleton and the cell membrane, for the development and maintenance of a paradigmatic neuronal circuit, the cerebellar cortex.
Study showed that MTSS1 regulates neurite outgrowth and dendritic arborization in primary neurons in vitro, possibly through a Rac1- and PIP (show PIP Proteins)-dependent pathway.
role of MIM in the homeostasis of BM cells, including HSPCs, through modulation of the CXCR4 (show CXCR4 Proteins)/SDF-1 (show CXCL12 Proteins) axis and interactions of BM leukocytes with their microenvironments.
Identify the inverse-BAR (I-BAR) protein MIM/MTSS1 as a nucleator of dendritic spines. MIM accumulated to future spine initiation sites in a PIP2-dependent manner and deformed the plasma membrane outward into a proto-protrusion via its I-BAR domain.
The data demonstrated for the first time an important role for missing-in-metastasis protein in B-cell development. There was a predisposition of missing-in-metastasis-null mice to develop diffuse large B lymphomas.
MTSS1 might be involved in shaping neuronal membranes in vivo.
endogenous MIM protein regulates globally the cell architecture and endocytosis that ultimately influence a variety of cellular behaviors, including cell polarity, motility, receptor signaling and membrane ruffling
MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia.
Results suggest that MIM promotes ciliogenesis by antagonizing Src (show SRC Proteins)-dependent phosphorylation of Cortactin (show CTTN Proteins) and describe a mechanism linking regulation of the actin cytoskeleton with ciliogenesis and Shh (show SHH Proteins) signaling during tissue regeneration.
tissue-specific regulator of cytoskeletal dynamics that interacts with ATP-actin monomers through its C-terminal WH2 domain
morphogenetic pathway involving Daam1 (show DAAM1 Proteins) and MIM that transduces non-canonical Wnt (show WNT2 Proteins) signaling for the cytoskeletal changes and membrane dynamics required for vertebrate neural tube closure
May be related to cancer progression or tumor metastasis in a variety of organ sites, most likely through an interaction with the actin cytoskeleton.
metastasis suppressor 1
, metastasis suppressor protein 1
, metastasis suppressor protein 1-like
, metastasis suppressor YGL-1
, missing in metastasis protein
, actin monomer-binding protein