Both Wnt and mTOR signaling pathways are involved in insulin-stimulated proto-oncogene expression in intestinal cells

Cellular Signalling

Volumn 20, Issue 1, 2008, Pages 219-229

  Sun, Jane ^a,b   Jin, Tianru ^a,b  

^a UNIVERSITY HEALTH NETWORK   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Beta catenin; c Myc; Insulin; mTOR; Wnt

Indexed keywords

BETA ACTIN; BETA CATENIN; HISTONE H3; INSULIN; MAMMALIAN TARGET OF RAPAMYCIN; MYC PROTEIN; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; WNT PROTEIN;

ANIMAL CELL; ARTICLE; CANCER CELL CULTURE; CELL PROLIFERATION; CELL STRAIN HT29; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; DRUG BINDING; DRUG EFFECT; ENZYME INHIBITION; GENE EXPRESSION; HUMAN; HUMAN CELL; INTESTINE CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; ONCOGENE C MYC; PRIORITY JOURNAL; PROTEIN BINDING; RAT; REPORTER GENE;

1-PHOSPHATIDYLINOSITOL 3-KINASE; ANIMALS; BETA CATENIN; CELL LINE; CELL LINE, TUMOR; CELL PROLIFERATION; COLORECTAL NEOPLASMS; HUMANS; HYPERINSULINISM; INSULIN; INTESTINES; PROTEIN KINASES; PROTO-ONCOGENE PROTEINS C-AKT; PROTO-ONCOGENE PROTEINS C-MYC; RATS; SIGNAL TRANSDUCTION; WNT PROTEINS;

RATTUS;

EID: 36248982703     PISSN: 08986568     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cellsig.2007.10.010     Document Type: Article

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