The Cell Killing Mechanisms of Hydroxyurea

被引:155
作者
Singh, Amanpreet [1 ,2 ]
Xu, Yong-Jie [1 ]
机构
[1] Wright State Univ, Boonshoft Sch Med, Dept Pharmacol & Toxicol, Dayton, OH 45435 USA
[2] NYSDOH, Wadsworth Ctr, 120 New Scotland Ave, Albany, NY 12208 USA
关键词
hydroxyurea; ribonucleotide reductase; oxidative stress; cytokinesis arrest; DNA replication checkpoint; cell cycle; MOUSE RIBONUCLEOTIDE REDUCTASE; DAMAGE-INDUCED PHOSPHORYLATION; CHINESE-HAMSTER CELLS; DNA-DAMAGE; ESCHERICHIA-COLI; HYDROGEN-PEROXIDE; SCHIZOSACCHAROMYCES-POMBE; MAMMALIAN-CELLS; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTOR;
D O I
10.3390/genes7110099
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hydroxyurea is a well-established inhibitor of ribonucleotide reductase that has a long history of scientific interest and clinical use for the treatment of neoplastic and non-neoplastic diseases. It is currently the staple drug for the management of sickle cell anemia and chronic myeloproliferative disorders. Due to its reversible inhibitory effect on DNA replication in various organisms, hydroxyurea is also commonly used in laboratories for cell cycle synchronization or generating replication stress. However, incubation with high concentrations or prolonged treatment with low doses of hydroxyurea can result in cell death and the DNA damage generated at arrested replication forks is generally believed to be the direct cause. Recent studies in multiple model organisms have shown that oxidative stress and several other mechanisms may contribute to the majority of the cytotoxic effect of hydroxyurea. This review aims to summarize the progress in our understanding of the cell-killing mechanisms of hydroxyurea, which may provide new insights towards the improvement of chemotherapies that employ this agent.
引用
收藏
页数:15
相关论文
共 136 条
[1]  
ADRAGNA NC, 1994, BLOOD, V83, P553
[2]   OVERPRODUCTION OF THE FREE-RADICAL OF RIBONUCLEOTIDE REDUCTASE IN HYDROXYUREA-RESISTANT MOUSE FIBROBLAST 3T6-CELLS [J].
AKERBLOM, L ;
EHRENBERG, A ;
GRASLUND, A ;
LANKINEN, H ;
REICHARD, P ;
THELANDER, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (04) :2159-2163
[3]   Replication in hydroxyurea: It's a matter of time [J].
Alvino, Gina M. ;
Collingwood, David ;
Murphy, John M. ;
Delrow, Jeffrey ;
Brewer, Bonita J. ;
Raghuraman, M. K. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (18) :6396-6406
[4]  
BARRANCO SC, 1974, CANCER RES, V34, P1616
[5]   Cytokinesis and the contractile ring in fission yeast: towards a systems-level understanding [J].
Bathe, Mark ;
Chang, Fred .
TRENDS IN MICROBIOLOGY, 2010, 18 (01) :38-45
[6]   The Oxidative Stress Responsive Transcription Factor Pap1 Confers DNA Damage Resistance on Checkpoint-Deficient Fission Yeast Cells [J].
Belfield, Carrie ;
Queenan, Craig ;
Rao, Hui ;
Kitamura, Kenji ;
Walworth, Nancy C. .
PLOS ONE, 2014, 9 (02)
[7]   The transcription factor Pap1/Caf3 plays a central role in the determination of caffeine resistance in Schizosaccharomyces pombe [J].
Benko, Z ;
Fenyvesvolgyi, C ;
Pesti, M ;
Sipiczki, M .
MOLECULAR GENETICS AND GENOMICS, 2004, 271 (02) :161-170
[8]  
BJORKLUND S, 1990, BIOCHEMISTRY-US, V29, P5452
[9]   Thiol-based H2O2 signalling in microbial systems [J].
Boronat, Susanna ;
Domenech, Alba ;
Paulo, Esther ;
Calvo, Isabel A. ;
Garcia-Santamarina, Sarela ;
Garcia, Patricia ;
Encinar del Dedo, Javier ;
Barcons, Anna ;
Serrano, Erica ;
Carmona, Merce ;
Hidalgo, Elena .
REDOX BIOLOGY, 2014, 2 :395-399
[10]   N-hydroxyurea as zinc binding group in matrix metalloproteinase inhibition:: Mode of binding in a complex with MMP-8 [J].
Campestre, C ;
Agamennone, M ;
Tortorella, P ;
Preziuso, S ;
Biasone, A ;
Gavuzzo, E ;
Pochetti, G ;
Mazza, F ;
Hiller, O ;
Tschesche, H ;
Consalvi, V ;
Gallina, C .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (01) :20-24