c-myc suppression in Burkitt's lymphoma cells

被引:49
作者
Simonsson, T
Henriksson, M
机构
[1] Karolinska Inst, Ctr Microbiol & Tumor Biol, SE-17177 Stockholm, Sweden
[2] Chalmers Univ Technol, Lundberg Lab, Dept Mol Biotechnol, SE-40530 Gothenburg, Sweden
关键词
anticancer drug; chromatin; G-quartet; gene therapy; promoter; telomere;
D O I
10.1006/bbrc.2001.6096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of the study was to elucidate how DNA tetraplex (also referred to as G-quadruplex)-forming oligonucleotides mediate suppression of the human c-myc gene at the level of transcription initiation. A 22-base-long oligonucleotide, which is rich in guanines and folds into an intrastrand DNA tetraplex under physiological conditions, was administered to a Burkitt's lymphoma cell line overexpressing a (8:14) translocated c-myc allele. Administration of the oligonucleotide at nanomolar concentrations to the surrounding medium resulted in efficient cellular uptake, and was accompanied by a substantial concentration and conformation-dependent decrease in growth rate. We discuss how c-myc transcription is initiated at the molecular level and speculate that the oligonucleotide exerts a dual effect on c-myc expression in vivo. (C) 2002 Elsevier Science.
引用
收藏
页码:11 / 15
页数:5
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