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Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines.

Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines. Research Abstract Details 

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  • Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines. Abstract Text:

    fumihiro takekawaFumihiro Takekawa,tatsuhito nagumoTatsuhito Nagumo,satoru shintaniSatoru Shintani,ken hashimotoKen Hashimoto,hirotaka kikuchiHirotaka Kikuchi,tadashi katayamaTadashi Katayama,mariko ishiharaMariko Ishihara,osamu amanoOsamu Amano,masami kawaseMasami Kawase,hiroshi sakagamiHiroshi Sakagami,fumihiro takekawaFumihiro Takekawa,tatsuhito nagumoTatsuhito Nagumo,satoru shintaniSatoru Shintani,ken hashimotoKen Hashimoto,hirotaka kikuchiHirotaka Kikuchi,tadashi katayamaTadashi Katayama,mariko ishiharaMariko Ishihara,osamu amanoOsamu Amano,masami kawaseMasami Kawase,hiroshi sakagamiHiroshi Sakagami,

    Fourteen 4-trifluoromethylimidazole derivatives were investigated for their cytotoxicity against three human normal cells (gingival fibroblast HGF, pulp cell HPC and periodontal ligament fibroblast HPLF) and four human tumor cell lines (oral squamous cell carcinoma HSC-2, HSC-3, HSC-4 and promyelocytic leukemia HL-60). Among these compounds, 4-trifluoromethyl-1,2-diphenylimidazole (IM5), 1-benzyl-4-trifluoromethyl-2-phenylimidazole (IM7) and 5-[1-ethoxy-2,2,2-trifluoro-1-(trifluoromethyl) ethyl]-1-methyl-2-phenyl-1H-imidazole (IM12) showed much higher cytotoxicity and tumor-specificity than the other compounds. IM5, the most potent compound, induced different types of cell death depending on the target cells. IM5 induced DNA fragmentation of oligonucleosomal units (a biochemical hallmark of apoptosis) in the HL-60 cells, but not in such a clear-cut laddering pattern in the HSC-2 cells. On the other hand, IM5 produced secondary lysosomes digesting broken organelles, without induction of internucleosomal DNA fragmentation and disappearance of cell surface microvilli in the HSC-4 cells, even though the HSC-2 and HSC-4 cells showed comparable sensitivity to IM5. These data suggest that the type of cell death is determined by the type of target cells, but not by the drug-sensitivity of the cells.

    Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines. Publishing Authors By Initials

    f takekawaF Takekawa,t nagumoT Nagumo,s shintaniS Shintani,k hashimotoK Hashimoto,h kikuchiH Kikuchi,t katayamaT Katayama,m ishiharaM Ishihara,o amanoO Amano,m kawaseM Kawase,h sakagamiH Sakagami,f takekawaF Takekawa,t nagumoT Nagumo,s shintaniS Shintani,k hashimotoK Hashimoto,h kikuchiH Kikuchi,t katayamaT Katayama,m ishiharaM Ishihara,o amanoO Amano,m kawaseM Kawase,h sakagamiH Sakagami,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE: 2007 Nov-Dec

    Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Anticancer research

    VOLUME: 27

    Page Numbers: 4065-9

    Journal Abbreviation: Anticancer Res.

    ISSN: 0250-7005

    DAY: 29

    MONTH: 01

    YEAR: 2008

    Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8102988

    Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines. Keywords Mesh Terms:

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    Grant and Affiliation Information for Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines.

    AFFILIATION: Division of Pharmacology, Meikai University School of Dentistry, Sakado, Saitama 350-0283, Japan.

    Country: Greece

    Greece Research PublicationGreece Research Publication

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    MEDLINETA: Anticancer Res

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