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Cytotoxicity, DNA binding and localisation of novel bis-naphthalimidopropyl polyamine derivatives.

作者信息

Pavlov V, Kong Thoo Lin P, Rodilla V

机构信息

School of Applied Sciences, The Robert Gordon University, St. Andrew Street, Aberdeen AB25 1HG, Scotland, UK.

出版信息

Chem Biol Interact. 2001 Jul 31;137(1):15-24. doi: 10.1016/s0009-2797(01)00165-x.

DOI:10.1016/s0009-2797(01)00165-x
PMID:11518561
Abstract

Bis-naphthalimidopropyl spermidine (BNIPSpd), spermine (BNIPSpm) and oxa-spermine (BNIPOSpm) showed high in vitro cytotoxicity against human breast cancer MCF-7 cells with IC(50) values of 1.38, 2.91 and 8.45 microM, respectively. These compounds were found to effectively displace the intercalating agent ethidium bromide bound to the calf thymus DNA using fluorimetric methods (C(50) 0.08-0.12 microM) and their apparent equilibrium binding constants (K(app)) were calculated to be in the range of 10.5-18 x 10(7) M(-1). Furthermore, strong stabilisation of calf thymus DNA duplex in the presence of bis-naphthalimidopropyl polyamine derivatives (BNIPSpd, BNIPSpm and BNIPOSpm) was observed by UV spectrophotometric analysis (T(m)=93.3-97 degrees C compared with 75 degrees C for calf thymus DNA without drug). Because of their inherent fluorescence, these compounds were localised preferentially inside the nucleus as evidenced by their direct observation under the fluorescence microscope. The results obtained suggest that the cytotoxic activity of the bis-naphthalimidopropyl polyamines may be in part, caused by their effects on DNA.

摘要

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