Polycyclic aromatic compounds as anticancer agents: Evaluation of synthesis and in vitro cytotoxicity

被引:41
作者
Bandyopadhyay, Debasish [2 ]
Granados, Jose C. [1 ]
Short, John D. [1 ,3 ]
Banik, Bimal K. [2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Div Med Res, Reg Acad Hlth Ctr, Edinburg, TX 78541 USA
[2] Univ Texas Pan Amer, Dept Chem, Edinburg, TX 78539 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Pharmacol, San Antonio, TX 78229 USA
关键词
polyaromatic; antitumor; cytotoxicity; liver cancer; emission spectrum; BETA-LACTAMS; DNA-INTERCALATORS; BIOLOGICAL EVALUATION; STAUDINGER-REACTION; ANTITUMOR-ACTIVITY; DIBENZOFLUORENE DERIVATIVES; SPECTRAL CHARACTERISTICS; ASYMMETRIC-SYNTHESIS; PYRENE; CHRYSENE;
D O I
10.3892/ol.2011.436
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Polycyclic aromatic hydrocarbons (PAHs) are considered to be significant environmental carcinogens. Additionally, various planar ring systems are capable of intercalating with DNA, leading to a number of drugs that possess chemotherapeutic activity. In this study, three new polyaromatic compounds with a side chain were synthesized, and spectroscopic as well as elemental analyses were performed. The addition of the long chains to either chrysene or pyrene caused a red-shift in the spectral emission when compared to the corresponding polycyclic aromatic hydrocarbons itself. Furthermore, the cytotoxicity of the three novel polyaromatic compounds was evaluated in vitro in a panel of cultured mammalian cell lines. The pyrenyl ether demonstrated better cytotoxicity compared to cisplatin against colon (HT-29) as well as cervical (HeLa) cancer cell lines. In conclusion, three new compounds were synthesized and investigated in this study. This novel method is likely to play a role in other areas of research.
引用
收藏
页码:45 / 49
页数:5
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