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4‐Amino‐5‐benzoyl‐2‐(4‐methoxyphenylamino)thiazole (DAT1): a cytotoxic agent towards cancer cells and a probe for tubulin‐microtubule system
Author(s) -
Sengupta Suparna,
Smitha Sasidharan L,
Thomas Nisha E,
Santhoshkumar Thankaiyyan R,
Devi Satyabhama K C,
Sreejalekshmi Kumaran G,
Rajasekharan Kallikat N
Publication year - 2005
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0706276
Subject(s) - tubulin , prometaphase , microtubule , mitosis , metaphase , vinblastine , microbiology and biotechnology , cytoskeleton , biology , colchicine , chemistry , biochemistry , cell , genetics , chromosome , chemotherapy , gene
1 Microtubule binding drugs are of special interest as they have important roles in the modulation of cellular functions and many of them act as anticancer agents. 4‐Amino‐5‐benzoyl‐2‐(4‐methoxyphenylamino)thiazole (DAT1) was identified as one of the active compounds from a series of diaminoketothiazoles in a cell‐based screening assay to discover cytotoxic compounds. 2 DAT1 shows cytotoxicity with GI 50 values ranging from 0.05 to 1 μ M in different malignant cell lines with an average value of 0.35 μ M . It blocks mitosis in the prometaphase and metaphase stages. In HeLa cells, DAT1 blocks the spindle function by disturbing spindle microtubule and chromosome organization. 3 The drug also inhibits assembly of brain microtubules and binds tubulin specifically at a single site with induction of fluorescence. The dissociation constant of DAT1 binding to tubulin was determined as 2.9±1 μ M at 24°C. The binding site of DAT1 on tubulin overlaps with that of the conventional colchicine‐binding site. 4 DAT1 can thus be considered as a lead compound of a new class of small molecules and this study can be used as a step to develop potent antimitotic agents for the control of cytoskeletal functions and cell proliferation. It would also be an interesting probe for the structure–function studies of tubulin–microtubule system.British Journal of Pharmacology (2005) 145 , 1076–1083. doi: 10.1038/sj.bjp.0706276 ; published online 13 June 2005