A novel protein associated with membrane-type1 matrix metalloproteinase binds p27kip1 and regulates RhoA activation, actin remodeling, and matrigel invasion

Journal of Biological Chemistry

Volumn 284, Issue 40, 2009, Pages 27315-27326

  Hoshino, Daisuke ^a   Tomari, Taizo ^a   Nagano, Makoto ^a   Koshikawa, Naohiko ^a   Seiki, Motoharu ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN CYTOSKELETON; CANCER THERAPY; CELL CYCLE REGULATORS; DOWN-REGULATION; GUANINE NUCLEOTIDE EXCHANGE FACTORS; HUMAN TUMOR CELLS; INVASION FRONT; LAMELLIPODIA; LYSOPHOSPHATIDIC ACID; MATRIX METALLOPROTEINASES; NOVEL PROTEINS; OVER-EXPRESSION; PERICELLULAR PROTEOLYSIS; TUMOR CELL INVASION;

CELL CULTURE; PHOSPHOLIPIDS; TUMORS; ULSI CIRCUITS;

CELL MEMBRANES;

ACTIN; CORTACTIN; CYCLIN DEPENDENT KINASE INHIBITOR 1B; GUANINE NUCLEOTIDE EXCHANGE FACTOR; LYSOPHOSPHATIDIC ACID; MATRIX METALLOPROTEINASE 14; RHOA GUANINE NUCLEOTIDE BINDING PROTEIN; CARRIER PROTEIN; COLLAGEN; GELATINASE A; GUANOSINE TRIPHOSPHATE; LAMININ; MATRIGEL; P27RF RHO PROTEIN, HUMAN; P27RF-RHO PROTEIN, HUMAN; PROTEOGLYCAN;

ARTICLE; CANCER INVASION; CELL INVASION; CELL STIMULATION; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CYTOPLASM; DOWN REGULATION; ENZYME ACTIVATION; ENZYME REGULATION; ENZYME RELEASE; GENE OVEREXPRESSION; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; TUMOR CELL; ANIMAL; DRUG ANTAGONISM; DRUG COMBINATION; DRUG POTENTIATION; ENZYME SPECIFICITY; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; TUMOR CELL LINE;

ACTINS; ANIMALS; CARRIER PROTEINS; CELL LINE, TUMOR; COLLAGEN; CONSERVED SEQUENCE; CYCLIN-DEPENDENT KINASE INHIBITOR P27; DRUG COMBINATIONS; ENZYME ACTIVATION; GENE EXPRESSION REGULATION; GUANOSINE TRIPHOSPHATE; HUMANS; LAMININ; MATRIX METALLOPROTEINASE 14; MATRIX METALLOPROTEINASE 2; PROTEOGLYCANS; RHOA GTP-BINDING PROTEIN; SUBSTRATE SPECIFICITY;

EID: 70350451708     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.041400     Document Type: Article

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