The hyposensitive N187D P2X7 mutant promotes malignant progression in nude mice

Journal of Biological Chemistry

Volumn 285, Issue 46, 2010, Pages 36179-36187

  Chong, Jing Hui ^a   Zheng, Guo Guang ^a   Ma, Yuan Yuan ^a   Zhang, Hai Yan ^a   Nie, Kun ^a   Lin, Yong Min ^a   Wu, Ke Fu ^a  

^a PEKING UNION MEDICAL COLLEGE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOGENESIS; APOPTOSIS; ATP-ASE ACTIVITY; BIOLOGICAL FUNCTIONS; CELL SURFACE EXPRESSION; CELL SURFACES; EXTRACELLULAR SPACE; IN-VITRO; INTERCELLULAR COMMUNICATIONS; K562 CELLS; LEUKEMIA CELLS; MALIGNANT PROGRESSION; NUDE MICE; PLASMA MEMBRANES; TUMOR TISSUES; WILD TYPES;

CELL CULTURE; CELL DEATH; CELL MEMBRANES; PHOSPHORYLATION; TUMORS;

HISTOLOGY;

ADENINE; ADENOSINE TRIPHOSPHATASE; CALCIUM ION; GUANINE; MITOGEN ACTIVATED PROTEIN KINASE; MONOCYTE CHEMOTACTIC PROTEIN 1; MUTANT PROTEIN; PURINERGIC P2X7 RECEPTOR; VASCULOTROPIN;

ANGIOGENESIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CALCIUM TRANSPORT; CANCER GROWTH; CANCER TISSUE; CELL PROLIFERATION; CELL STRAIN K 562; CELL SURFACE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME PHOSPHORYLATION; EXTRACELLULAR SPACE; GENETIC TRANSFECTION; HEMATOLOGIC MALIGNANCY; HUMAN; HUMAN CELL; IN VITRO STUDY; IN VIVO STUDY; LEUKEMIA CELL J6 1; LEUKEMIA CELL LINE; MACROPHAGE; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEIC ACID BASE SUBSTITUTION; NUDE MOUSE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ADENOSINE TRIPHOSPHATE; ANIMALS; BLOTTING, WESTERN; CALCIUM; CELL LINE, TUMOR; DISEASE PROGRESSION; ENZYME ACTIVATION; FEMALE; GENE EXPRESSION REGULATION, LEUKEMIC; HUMANS; INTRACELLULAR SPACE; K562 CELLS; LEUKEMIA, EXPERIMENTAL; MACROPHAGES; MAP KINASE SIGNALING SYSTEM; MICE; MICE, INBRED BALB C; MICE, NUDE; MUTATION, MISSENSE; NEOVASCULARIZATION, PATHOLOGIC; P38 MITOGEN-ACTIVATED PROTEIN KINASES; RECEPTORS, PURINERGIC P2X7; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TRANSPLANTATION, HETEROLOGOUS; TUMOR BURDEN;

MUS MUSCULUS;

EID: 78149263196     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.128488     Document Type: Article

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