Combination treatment with HER-2 and VEGF peptide mimics induces potent anti-tumor and anti-angiogenic

Journal of Biological Chemistry

Volumn 286, Issue 15, 2011, Pages 13626-13637

  Foy, Kevin C ^a   Liu, Zhenzhen ^b   Phillips, Gary ^c   Miller, Megan ^a,b   Kaumaya, Pravin T P ^a,b,c  

^a Department of Microbiology ^*  (United States)

^b OHIO STATE UNIVERSITY   (United States)

^c OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOGENESIS; ANTI-TUMORS; BALB/C MICE; BEVACIZUMAB; BLOCKING RECEPTORS; BREAST CANCER; CANCER TREATMENT; CELL VIABILITY; COMBINATION TREATMENTS; DEGRADABILITY; HUMANIZED MONOCLONAL ANTIBODY; IN-VITRO; IN-VIVO; L-AMINO ACIDS; OVER-EXPRESSION; PEPTIDE MIMICS; PROTEIN LEVEL; TUMOR GROWTH; VEGFR-2;

AMINO ACIDS; ASSAYS; DISEASES; MONOCLONAL ANTIBODIES; PHOSPHORYLATION; RNA; TUMORS;

PEPTIDES;

EPIDERMAL GROWTH FACTOR RECEPTOR 2; EPIDERMAL GROWTH FACTOR RECEPTOR 2[266-296]; MATRIGEL; PERTUZUMAB; SYNTHETIC PEPTIDE; UNCLASSIFIED DRUG; VASCULOTROPIN; VASCULOTROPIN RECEPTOR 2; VASCULOTROPIN[76-96];

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIANGIOGENIC ACTIVITY; ANTINEOPLASTIC ACTIVITY; ARTICLE; BIODEGRADABILITY; BREAST CANCER; CANCER CELL CULTURE; CANCER INHIBITION; CELL PROLIFERATION; CELL VIABILITY; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG DESIGN; DRUG DETERMINATION; DRUG POTENCY; DRUG RECEPTOR BINDING; DRUG STRUCTURE; DRUG SYNTHESIS; DRUG TARGETING; IN VITRO STUDY; IN VIVO STUDY; MOUSE; NONHUMAN; PEPTIDE ANALYSIS; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SIGNAL TRANSDUCTION;

ANGIOGENESIS INHIBITORS; ANIMALS; ANTIBODIES, MONOCLONAL; ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS; BIOMIMETIC MATERIALS; DRUG SCREENING ASSAYS, ANTITUMOR; FEMALE; HUMANS; MICE; MICE, INBRED BALB C; NEOPLASMS, EXPERIMENTAL; PEPTIDES; RECEPTOR, ERBB-2; VASCULAR ENDOTHELIAL GROWTH FACTOR A;

EID: 79953859123     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.216820     Document Type: Article

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