Stat3 activation is required for the growth of U87 cell-derived tumours in mice

European Journal of Cancer

Volumn 45, Issue 4, 2009, Pages 677-684

  Dasgupta, Atreyi ^a   Raychaudhuri, Baisakhi ^a   Haqqi, Talat ^a   Prayson, Richard ^a   Van Meir, Erwin G ^b   Vogelbaum, Michael ^a   Haque, Saikh Jaharul ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Angiogenesis; Apoptosis; Glioblastoma multiforme; Hypoxia; Stat3; VEGF

Indexed keywords

STAT3 PROTEIN;

ANGIOGENESIS; ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; CANCER CELL CULTURE; CANCER INHIBITION; CELL CLONE; CELL CLONING; CONTROLLED STUDY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNE DEFICIENCY; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; TUMOR CELL; TUMOR GROWTH; VECTOR CONTROL;

ANIMALS; APOPTOSIS; CELL HYPOXIA; CELL PROLIFERATION; DISEASE MODELS, ANIMAL; DISEASE PROGRESSION; ELECTROPHORETIC MOBILITY SHIFT ASSAY; GENETIC VECTORS; GLIOBLASTOMA; HUMANS; IMMUNOCOMPROMISED HOST; MICE; MICE, NUDE; NEOPLASM PROTEINS; NEOPLASM TRANSPLANTATION; NEOVASCULARIZATION, PATHOLOGIC; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; STAT3 TRANSCRIPTION FACTOR; SURVIVAL ANALYSIS; TRANSPLANTATION, HETEROLOGOUS; TUMOR CELLS, CULTURED;

EID: 60349107511     PISSN: 09598049     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejca.2008.11.027     Document Type: Article

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