Feriotto G, Nastruzzi C, Mischiati C, Gambari R
UNIV FERRARA,IST CHIM BIOL,VIA L BORSARI N46,I-44100 FERRARA,ITALY. UNIV FERRARA,DIPARTIMENTO SCI FARMACEUT,I-44100 FERRARA,ITALY. CTR INTERDIPARTIMENTALE BIOTECNOL,I-44100 FERRARA,ITALY.
Int J Oncol. 1992 Aug;1(3):277-81. doi: 10.3892/ijo.1.3.277.
The pharmacological-mediated inhibition of the interaction between regulatory proteins and target DNA sequences could represent a potential experimental strategy to control growth of neoplastic cells, viral DNA replication and biological life cycle of infectious microorganisms. Aromatic polyamidines are powerful inhibitors of DNA-protein interactions, in vitro proliferation of tumor cell lines and in vivo growth of tumorigenic cells xenografted into nude mice. In order to obtain more detailed information on structure-activity relationships, we have analysed the effects of different aromatic polyamidines on the binding of a recombinant protein, the Epstein-Barr Virus (EBV) Nuclear Antigen 1 (EBNA-1) to the DNA target sequence of EBV, containing the 12 bp palindromic consensus TAGCATATGCTA sequence. The results obtained suggest that aromatic polyamidines differentially inhibit the interactions between DNA-binding proteins and target DNA sequences, leading to differential effects on tumor cell growth.
通过药理学方法抑制调节蛋白与靶DNA序列之间的相互作用,可能是一种控制肿瘤细胞生长、病毒DNA复制以及感染性微生物生物生命周期的潜在实验策略。芳香族聚脒是DNA-蛋白质相互作用、肿瘤细胞系体外增殖以及接种于裸鼠体内的致瘤细胞体内生长的强力抑制剂。为了获取更多关于构效关系的详细信息,我们分析了不同芳香族聚脒对重组蛋白——爱泼斯坦-巴尔病毒(EBV)核抗原1(EBNA-1)与EBV的DNA靶序列(包含12bp回文共有序列TAGCATATGCTA)结合的影响。所得结果表明,芳香族聚脒可不同程度地抑制DNA结合蛋白与靶DNA序列之间的相互作用,从而对肿瘤细胞生长产生不同影响。