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High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects

BACKGROUND: PARP-1 plays a critical role in DNA damage repair and contributes to progression of cancer. To explore the role of PARP-1 in acute myeloid leukemia (AML), we analyzed the expression of PARP-1 in AML and its relation to the clinical prognosis. Then, we investigated the efficacy and mechan...

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Autores principales: Li, Xia, Li, Chenying, Jin, Jingrui, Wang, Jinghan, Huang, Jiansong, Ma, Zhixin, Huang, Xin, He, Xiao, Zhou, Yile, Xu, Yu, Yu, Mengxia, Huang, Shujuan, Yan, Xiao, Li, Fenglin, Pan, Jiajia, Wang, Yungui, Yu, Yongping, Jin, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306376/
https://www.ncbi.nlm.nih.gov/pubmed/30472087
http://dx.doi.org/10.1016/j.ebiom.2018.11.025
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author Li, Xia
Li, Chenying
Jin, Jingrui
Wang, Jinghan
Huang, Jiansong
Ma, Zhixin
Huang, Xin
He, Xiao
Zhou, Yile
Xu, Yu
Yu, Mengxia
Huang, Shujuan
Yan, Xiao
Li, Fenglin
Pan, Jiajia
Wang, Yungui
Yu, Yongping
Jin, Jie
author_facet Li, Xia
Li, Chenying
Jin, Jingrui
Wang, Jinghan
Huang, Jiansong
Ma, Zhixin
Huang, Xin
He, Xiao
Zhou, Yile
Xu, Yu
Yu, Mengxia
Huang, Shujuan
Yan, Xiao
Li, Fenglin
Pan, Jiajia
Wang, Yungui
Yu, Yongping
Jin, Jie
author_sort Li, Xia
collection PubMed
description BACKGROUND: PARP-1 plays a critical role in DNA damage repair and contributes to progression of cancer. To explore the role of PARP-1 in acute myeloid leukemia (AML), we analyzed the expression of PARP-1 in AML and its relation to the clinical prognosis. Then, we investigated the efficacy and mechanism of PARP inhibitor BMN673 (Talazoparib) combined with NL101, a novel SAHA-bendamustine hybrid in vitro and in vivo. METHODS: The expression of PARP-1 in 339 cytogenetically normal AML (CN-AML) cases was evaluated using RT-PCR. According to the expression of PARP-1, the clinical characteristics and prognosis of the patients were grouped and compared. The combination effects of BMN673 and NL101 were studied in AML cells and B-NSG mice xenograft model of MV4-11. FINDINGS: We found patients in high PARP-1 expression group had higher levels of blast cells in bone marrow (P = .003) and white blood cells (WBC) in peripheral blood (P = .008), and were associated with a more frequent FLT3-ITD mutation (28.2% vs 17.3%, P = .031). The overall survival (OS) and event free survival (EFS) of the high expression group were significantly shorter than those in the low expression group (OS, P = .005 and EFS, P = .004). BMN673 combined with NL101 had a strong synergistic effect in treating AML. The combination significantly induced cell apoptosis and arrested cell cycle in G2/M phase. Mechanistically, BMN673 and NL101 combinatorial treatment promoted DNA damage. In vivo, the combination effectively delayed the development of AML and prolonged survival. INTERPRETATION: High PARP-1 expression predicts poor survival in CN-AML patients. The synergistic effects of PARP inhibitor BMN673 in combination with SAHA-bendamustine hybrid, NL101, provide a new therapeutic strategy against AML. FUND: National Natural Science Foundation of China and Zhejiang Provincial Key Innovation Team.
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spelling pubmed-63063762018-12-28 High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects Li, Xia Li, Chenying Jin, Jingrui Wang, Jinghan Huang, Jiansong Ma, Zhixin Huang, Xin He, Xiao Zhou, Yile Xu, Yu Yu, Mengxia Huang, Shujuan Yan, Xiao Li, Fenglin Pan, Jiajia Wang, Yungui Yu, Yongping Jin, Jie EBioMedicine Research paper BACKGROUND: PARP-1 plays a critical role in DNA damage repair and contributes to progression of cancer. To explore the role of PARP-1 in acute myeloid leukemia (AML), we analyzed the expression of PARP-1 in AML and its relation to the clinical prognosis. Then, we investigated the efficacy and mechanism of PARP inhibitor BMN673 (Talazoparib) combined with NL101, a novel SAHA-bendamustine hybrid in vitro and in vivo. METHODS: The expression of PARP-1 in 339 cytogenetically normal AML (CN-AML) cases was evaluated using RT-PCR. According to the expression of PARP-1, the clinical characteristics and prognosis of the patients were grouped and compared. The combination effects of BMN673 and NL101 were studied in AML cells and B-NSG mice xenograft model of MV4-11. FINDINGS: We found patients in high PARP-1 expression group had higher levels of blast cells in bone marrow (P = .003) and white blood cells (WBC) in peripheral blood (P = .008), and were associated with a more frequent FLT3-ITD mutation (28.2% vs 17.3%, P = .031). The overall survival (OS) and event free survival (EFS) of the high expression group were significantly shorter than those in the low expression group (OS, P = .005 and EFS, P = .004). BMN673 combined with NL101 had a strong synergistic effect in treating AML. The combination significantly induced cell apoptosis and arrested cell cycle in G2/M phase. Mechanistically, BMN673 and NL101 combinatorial treatment promoted DNA damage. In vivo, the combination effectively delayed the development of AML and prolonged survival. INTERPRETATION: High PARP-1 expression predicts poor survival in CN-AML patients. The synergistic effects of PARP inhibitor BMN673 in combination with SAHA-bendamustine hybrid, NL101, provide a new therapeutic strategy against AML. FUND: National Natural Science Foundation of China and Zhejiang Provincial Key Innovation Team. Elsevier 2018-11-22 /pmc/articles/PMC6306376/ /pubmed/30472087 http://dx.doi.org/10.1016/j.ebiom.2018.11.025 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Li, Xia
Li, Chenying
Jin, Jingrui
Wang, Jinghan
Huang, Jiansong
Ma, Zhixin
Huang, Xin
He, Xiao
Zhou, Yile
Xu, Yu
Yu, Mengxia
Huang, Shujuan
Yan, Xiao
Li, Fenglin
Pan, Jiajia
Wang, Yungui
Yu, Yongping
Jin, Jie
High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
title High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
title_full High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
title_fullStr High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
title_full_unstemmed High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
title_short High PARP-1 expression predicts poor survival in acute myeloid leukemia and PARP-1 inhibitor and SAHA-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
title_sort high parp-1 expression predicts poor survival in acute myeloid leukemia and parp-1 inhibitor and saha-bendamustine hybrid inhibitor combination treatment synergistically enhances anti-tumor effects
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306376/
https://www.ncbi.nlm.nih.gov/pubmed/30472087
http://dx.doi.org/10.1016/j.ebiom.2018.11.025
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