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Cancer Lett ; 212(2): 185-94, 2004 Aug 30.
Article in English | MEDLINE | ID: mdl-15279899

ABSTRACT

Mammalian myeloid and epithelial cells express many antimicrobiotic peptides that contribute to innate host defense against invading microbes. In the present study, a 27-mer peptide of the C-terminal domain (hCAP18(109-135)) and analogs of the antimicrobial peptide human cathelicidin LL-37/human cationic antimicrobial protein 18 (hCAP18) were examined for tumoricidal activity. In vitro results showed that hCAP18(109-135) induced apoptosis in human oral squamous cell carcinoma (OSCC), SAS-H1 cells. The hCAP18(109-135) induced mitochondrial depolarization and apoptosis in SAS-H1 cells, but not in healthy human gingival fibroblasts (HGF) and human keratinocyte line HaCaT cells. Caspases were not activated during hCAP18(109-135)-induced apoptosis in SAS-H1 cells. The results indicate that hCAP18(109-135) may induce caspase-independent apoptosis in OSCC but not in normal cells. hCAP18(109-135) can therefore be a useful anti-tumor therapeutic agent in the treatment of OSCC.


Subject(s)
Anti-Infective Agents/pharmacology , Antimicrobial Cationic Peptides/chemistry , Antimicrobial Cationic Peptides/pharmacology , Apoptosis , Peptides/chemistry , Carcinoma, Squamous Cell/drug therapy , Carcinoma, Squamous Cell/pathology , Caspase 3 , Caspases/metabolism , Cathelicidins , Cell Death , Cell Line, Tumor , Cells, Cultured , DNA/metabolism , DNA Fragmentation , Dose-Response Relationship, Drug , Enzyme Activation , Fibroblasts/metabolism , Humans , Membrane Potentials , Mitochondria/metabolism , Mitochondria/pathology , Mouth Neoplasms/drug therapy , Mouth Neoplasms/pathology , Protein Structure, Tertiary , Time Factors
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