Pancreatic cancer cells respond to type I collagen by inducing snail expression to promote membrane type 1 matrix metalloproteinase-dependent collagen invasion

Journal of Biological Chemistry

Volumn 286, Issue 12, 2011, Pages 10495-10504

  Shields, Mario A ^a   Dangi Garimella, Surabhi ^a   Krantz, Seth B ^a   Bentrem, David J ^a,b   Munshi, Hidayatullah G ^a,b  

^a NORTHWESTERN UNIVERSITY   (United States)

^b JESSE BROWN VA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CANCER INVASION; COLLAGEN GELS; DUCTAL ADENOCARCINOMAS; EPITHELIAL-MESENCHYMAL TRANSITION; IN-VIVO; MAPK SIGNALING; MATRIX METALLOPROTEINASES; MEMBRANE TYPE-1 MATRIX METALLOPROTEINASE; MEMBRANE TYPES; OVER-EXPRESSION; PANCREATIC CANCERS; POSITIVE CORRELATIONS; TISSUE CULTURE PLASTICS; TYPE I COLLAGEN;

ANIMALS; CELL CULTURE; CELLS; DISEASES; ENZYME ACTIVITY; GELS; SIGNALING; THREE DIMENSIONAL; TISSUE CULTURE; TUMORS;

COLLAGEN;

COLLAGEN GEL; COLLAGEN TYPE 1; MATRIX METALLOPROTEINASE 14; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; SMAD2 PROTEIN; SMAD3 PROTEIN; SMAD4 PROTEIN; TRANSCRIPTION FACTOR SNAIL; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1;

ARTICLE; CANCER CELL; CANCER GROWTH; CANCER INVASION; CONTROLLED STUDY; HUMAN; HUMAN TISSUE; IN VIVO STUDY; PANCREAS ADENOCARCINOMA; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN INDUCTION; SIGNAL TRANSDUCTION;

ADENOCARCINOMA; CARCINOMA, PANCREATIC DUCTAL; CELL LINE, TRANSFORMED; COLLAGEN TYPE I; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GENE EXPRESSION REGULATION, NEOPLASTIC; HUMANS; MAP KINASE SIGNALING SYSTEM; MATRIX METALLOPROTEINASE 14; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 3; NEOPLASM INVASIVENESS; NEOPLASM PROTEINS; PROTEIN-SERINE-THREONINE KINASES; RECEPTORS, TRANSFORMING GROWTH FACTOR BETA; SMAD PROTEINS; TRANSCRIPTION FACTORS;

GASTROPODA;

EID: 79953230450     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.195628     Document Type: Article

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