author_facet Aimiuwu, Josephine
Wang, Hongyan
Chen, Ping
Xie, Zhiliang
Wang, Jiang
Liu, Shujun
Klisovic, Rebecca
Mims, Alice
Blum, William
Marcucci, Guido
Chan, Kenneth K.
Aimiuwu, Josephine
Wang, Hongyan
Chen, Ping
Xie, Zhiliang
Wang, Jiang
Liu, Shujun
Klisovic, Rebecca
Mims, Alice
Blum, William
Marcucci, Guido
Chan, Kenneth K.
author Aimiuwu, Josephine
Wang, Hongyan
Chen, Ping
Xie, Zhiliang
Wang, Jiang
Liu, Shujun
Klisovic, Rebecca
Mims, Alice
Blum, William
Marcucci, Guido
Chan, Kenneth K.
spellingShingle Aimiuwu, Josephine
Wang, Hongyan
Chen, Ping
Xie, Zhiliang
Wang, Jiang
Liu, Shujun
Klisovic, Rebecca
Mims, Alice
Blum, William
Marcucci, Guido
Chan, Kenneth K.
Blood
RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
Cell Biology
Hematology
Immunology
Biochemistry
author_sort aimiuwu, josephine
spelling Aimiuwu, Josephine Wang, Hongyan Chen, Ping Xie, Zhiliang Wang, Jiang Liu, Shujun Klisovic, Rebecca Mims, Alice Blum, William Marcucci, Guido Chan, Kenneth K. 0006-4971 1528-0020 American Society of Hematology Cell Biology Hematology Immunology Biochemistry http://dx.doi.org/10.1182/blood-2011-11-382226 <jats:title>Abstract</jats:title> <jats:p>5-Azacytidine (5-azaC) is an azanucleoside approved for myelodysplastic syndrome. Approximately 80%-90% of 5-azaC is believed to be incorporated into RNA, which disrupts nucleic acid and protein metabolism leading to apoptosis. A smaller fraction (10%-20%) of 5-azaC inhibits DNA methylation and synthesis through conversion to decitabine triphosphate and subsequent DNA incorporation. However, its precise mechanism of action remains unclear. Ribonucleotide reductase (RR) is a highly regulated enzyme comprising 2 subunits, RRM1 and RRM2, that provides the deoxyribonucleotides required for DNA synthesis/repair. In the present study, we found for the first time that 5-azaC is a potent inhibitor of RRM2 in leukemia cell lines, in a mouse model, and in BM mononuclear cells from acute myeloid leukemia (AML) patients. 5-azaC–induced RRM2 gene expression inhibition involves its direct RNA incorporation and an attenuated RRM2 mRNA stability. Therefore, 5-azaC causes a major perturbation of deoxyribonucleotide pools. We also demonstrate herein that the initial RR-mediated 5-azaC conversion to decitabine is terminated through its own inhibition. In conclusion, we identify RRM2 as a novel molecular target of 5-azaC in AML. Our findings provide a basis for its more widespread clinical use either alone or in combination.</jats:p> RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia Blood
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title RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_unstemmed RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_full RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_fullStr RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_full_unstemmed RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_short RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_sort rna-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
topic Cell Biology
Hematology
Immunology
Biochemistry
url http://dx.doi.org/10.1182/blood-2011-11-382226
publishDate 2012
physical 5229-5238
description <jats:title>Abstract</jats:title> <jats:p>5-Azacytidine (5-azaC) is an azanucleoside approved for myelodysplastic syndrome. Approximately 80%-90% of 5-azaC is believed to be incorporated into RNA, which disrupts nucleic acid and protein metabolism leading to apoptosis. A smaller fraction (10%-20%) of 5-azaC inhibits DNA methylation and synthesis through conversion to decitabine triphosphate and subsequent DNA incorporation. However, its precise mechanism of action remains unclear. Ribonucleotide reductase (RR) is a highly regulated enzyme comprising 2 subunits, RRM1 and RRM2, that provides the deoxyribonucleotides required for DNA synthesis/repair. In the present study, we found for the first time that 5-azaC is a potent inhibitor of RRM2 in leukemia cell lines, in a mouse model, and in BM mononuclear cells from acute myeloid leukemia (AML) patients. 5-azaC–induced RRM2 gene expression inhibition involves its direct RNA incorporation and an attenuated RRM2 mRNA stability. Therefore, 5-azaC causes a major perturbation of deoxyribonucleotide pools. We also demonstrate herein that the initial RR-mediated 5-azaC conversion to decitabine is terminated through its own inhibition. In conclusion, we identify RRM2 as a novel molecular target of 5-azaC in AML. Our findings provide a basis for its more widespread clinical use either alone or in combination.</jats:p>
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author Aimiuwu, Josephine, Wang, Hongyan, Chen, Ping, Xie, Zhiliang, Wang, Jiang, Liu, Shujun, Klisovic, Rebecca, Mims, Alice, Blum, William, Marcucci, Guido, Chan, Kenneth K.
author_facet Aimiuwu, Josephine, Wang, Hongyan, Chen, Ping, Xie, Zhiliang, Wang, Jiang, Liu, Shujun, Klisovic, Rebecca, Mims, Alice, Blum, William, Marcucci, Guido, Chan, Kenneth K., Aimiuwu, Josephine, Wang, Hongyan, Chen, Ping, Xie, Zhiliang, Wang, Jiang, Liu, Shujun, Klisovic, Rebecca, Mims, Alice, Blum, William, Marcucci, Guido, Chan, Kenneth K.
author_sort aimiuwu, josephine
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container_title Blood
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description <jats:title>Abstract</jats:title> <jats:p>5-Azacytidine (5-azaC) is an azanucleoside approved for myelodysplastic syndrome. Approximately 80%-90% of 5-azaC is believed to be incorporated into RNA, which disrupts nucleic acid and protein metabolism leading to apoptosis. A smaller fraction (10%-20%) of 5-azaC inhibits DNA methylation and synthesis through conversion to decitabine triphosphate and subsequent DNA incorporation. However, its precise mechanism of action remains unclear. Ribonucleotide reductase (RR) is a highly regulated enzyme comprising 2 subunits, RRM1 and RRM2, that provides the deoxyribonucleotides required for DNA synthesis/repair. In the present study, we found for the first time that 5-azaC is a potent inhibitor of RRM2 in leukemia cell lines, in a mouse model, and in BM mononuclear cells from acute myeloid leukemia (AML) patients. 5-azaC–induced RRM2 gene expression inhibition involves its direct RNA incorporation and an attenuated RRM2 mRNA stability. Therefore, 5-azaC causes a major perturbation of deoxyribonucleotide pools. We also demonstrate herein that the initial RR-mediated 5-azaC conversion to decitabine is terminated through its own inhibition. In conclusion, we identify RRM2 as a novel molecular target of 5-azaC in AML. Our findings provide a basis for its more widespread clinical use either alone or in combination.</jats:p>
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spelling Aimiuwu, Josephine Wang, Hongyan Chen, Ping Xie, Zhiliang Wang, Jiang Liu, Shujun Klisovic, Rebecca Mims, Alice Blum, William Marcucci, Guido Chan, Kenneth K. 0006-4971 1528-0020 American Society of Hematology Cell Biology Hematology Immunology Biochemistry http://dx.doi.org/10.1182/blood-2011-11-382226 <jats:title>Abstract</jats:title> <jats:p>5-Azacytidine (5-azaC) is an azanucleoside approved for myelodysplastic syndrome. Approximately 80%-90% of 5-azaC is believed to be incorporated into RNA, which disrupts nucleic acid and protein metabolism leading to apoptosis. A smaller fraction (10%-20%) of 5-azaC inhibits DNA methylation and synthesis through conversion to decitabine triphosphate and subsequent DNA incorporation. However, its precise mechanism of action remains unclear. Ribonucleotide reductase (RR) is a highly regulated enzyme comprising 2 subunits, RRM1 and RRM2, that provides the deoxyribonucleotides required for DNA synthesis/repair. In the present study, we found for the first time that 5-azaC is a potent inhibitor of RRM2 in leukemia cell lines, in a mouse model, and in BM mononuclear cells from acute myeloid leukemia (AML) patients. 5-azaC–induced RRM2 gene expression inhibition involves its direct RNA incorporation and an attenuated RRM2 mRNA stability. Therefore, 5-azaC causes a major perturbation of deoxyribonucleotide pools. We also demonstrate herein that the initial RR-mediated 5-azaC conversion to decitabine is terminated through its own inhibition. In conclusion, we identify RRM2 as a novel molecular target of 5-azaC in AML. Our findings provide a basis for its more widespread clinical use either alone or in combination.</jats:p> RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia Blood
spellingShingle Aimiuwu, Josephine, Wang, Hongyan, Chen, Ping, Xie, Zhiliang, Wang, Jiang, Liu, Shujun, Klisovic, Rebecca, Mims, Alice, Blum, William, Marcucci, Guido, Chan, Kenneth K., Blood, RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia, Cell Biology, Hematology, Immunology, Biochemistry
title RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_full RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_fullStr RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_full_unstemmed RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_short RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_sort rna-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
title_unstemmed RNA-dependent inhibition of ribonucleotide reductase is a major pathway for 5-azacytidine activity in acute myeloid leukemia
topic Cell Biology, Hematology, Immunology, Biochemistry
url http://dx.doi.org/10.1182/blood-2011-11-382226