Yeast as a model organism for studying the actions of DNA topoisomerase-targeted drugs
被引:48
作者:
Reid, RJD
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机构:Thomas Jefferson Univ, Dept Mol Pharmacol & Biochem, Philadelphia, PA 19107 USA
Reid, RJD
Benedetti, P
论文数: 0引用数: 0
h-index: 0
机构:Thomas Jefferson Univ, Dept Mol Pharmacol & Biochem, Philadelphia, PA 19107 USA
Benedetti, P
Bjornsti, MA
论文数: 0引用数: 0
h-index: 0
机构:Thomas Jefferson Univ, Dept Mol Pharmacol & Biochem, Philadelphia, PA 19107 USA
Bjornsti, MA
机构:
[1] Thomas Jefferson Univ, Dept Mol Pharmacol & Biochem, Philadelphia, PA 19107 USA
[2] CNR, Ist Biol Cellulare, I-00137 Rome, Italy
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
|
1998年
/
1400卷
/
1-3期
关键词:
yeast;
Saccharomyces cerevisiae;
camptothecin;
DNA topoisomerase;
drug resistance;
genetics;
D O I:
10.1016/S0167-4781(98)00142-0
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 budding yeast Saccharomyces cerevisiae has been exploited to investigate the cytotoxic mechanisms of drugs that target DNA topoisomerases. This model organism has been used to establish eukaryotic DNA topoisomerase I or II as the cellular target of specific antineoplastic agents, to define mutations in these enzymes that confer drug resistance and to elucidate the cellular factors that modulate cell sensitivity to DNA topoisomerase-targeted drugs. These findings have provided valuable insights into the critical activities of these enzymes and how perturbing their functions produces DNA damage and cell death. 0167-4781/98/$ - see front matter (C) 1998 Elsevier Science B.V. All rights reserved.