Overexpression of collagenase 1 (MMP-1) is mediated by the ERK pathway in invasive melanoma cells. Role of BRAF mutation and fibroblast growth factor signaling

Journal of Biological Chemistry

Volumn 279, Issue 32, 2004, Pages 33168-33176

  Huntington, Jonathan T ^a   Shields, Janiel M ^b   Der, Channing J ^b   Wyatt, Colby A ^a   Benbow, Ulrike ^a,d   Slingluff Jr , Craig L ^c   Brinckerhoff, Constance E ^a  

^a DARTMOUTH MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF VIRGINIA   (United States)

^d UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; DEGRADATION; MATRIX ALGEBRA; MUTAGENESIS; THICKNESS MEASUREMENT; TUMORS;

ERK PATHWAY; MATRIX METALLOPROTEINASE (MMP); MELANOMA CELLS; MITOGEN-ACTIVATED PROTEIN KINASE (MAPK);

COLLAGEN;

COLLAGEN; FIBROBLAST GROWTH FACTOR; INTERSTITIAL COLLAGENASE; MATRIX METALLOPROTEINASE; MITOGEN ACTIVATED PROTEIN KINASE; RAF PROTEIN; RAS PROTEIN;

ARTICLE; AUTOCRINE EFFECT; BRAF GENE; CANCER INVASION; CANCER SURVIVAL; CELL PROLIFERATION; CELL SURVIVAL; DISEASE FREE SURVIVAL; ENZYME ACTIVATION; ENZYME SYNTHESIS; EXTRACELLULAR MATRIX; GENE; GENE MUTATION; GENE OVEREXPRESSION; HUMAN; HUMAN CELL; MELANOMA; MELANOMA CELL; METASTASIS; METASTASIS POTENTIAL; PRIORITY JOURNAL; PROTEIN DEGRADATION; SIGNAL TRANSDUCTION; TUMOR GROWTH;

ARSENITES; DISEASE-FREE SURVIVAL; ENZYME ACTIVATION; FIBROBLAST GROWTH FACTORS; GENE EXPRESSION; HUMANS; MAP KINASE KINASE 1; MAP KINASE KINASE 2; MATRIX METALLOPROTEINASE 1; MELANOMA; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 3; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; MITOGEN-ACTIVATED PROTEIN KINASES; MUTATION; NEOPLASM INVASIVENESS; PHOSPHORYLATION; PROGNOSIS; PROTEIN-TYROSINE KINASES; PROTO-ONCOGENE PROTEINS B-RAF; PROTO-ONCOGENE PROTEINS C-RAF; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; SIGNAL TRANSDUCTION; SODIUM COMPOUNDS; TUMOR CELLS, CULTURED;

EID: 4043139430     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M405102200     Document Type: Article

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