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血液系统恶性肿瘤的表观突变图谱作为新型表观遗传疗法的诱人靶点。

Epimutational profile of hematologic malignancies as attractive target for new epigenetic therapies.

作者信息

Fratta Elisabetta, Montico Barbara, Rizzo Aurora, Colizzi Francesca, Sigalotti Luca, Dolcetti Riccardo

机构信息

Cancer Bio-Immunotherapy Unit, Centro di Riferimento Oncologico, IRCCS, National Cancer Institute, Aviano, PN, Italy.

University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Australia.

出版信息

Oncotarget. 2016 Aug 30;7(35):57327-57350. doi: 10.18632/oncotarget.10033.

DOI:10.18632/oncotarget.10033
PMID:27329599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5302993/
Abstract

In recent years, recurrent somatic mutations in epigenetic regulators have been identified in patients with hematological malignancies. Furthermore, chromosomal translocations in which the fusion protein partners are themselves epigenetic regulators or where epigenetic regulators are recruited/targeted by oncogenic fusion proteins have also been described. Evidence has accumulated showing that "epigenetic drugs" are likely to provide clinical benefits in several hematological malignancies, granting their approval for the treatment of myelodysplastic syndromes and cutaneous T-cell lymphomas. A large number of pre-clinical and clinical trials evaluating epigenetic drugs alone or in combination therapies are ongoing. The aim of this review is to provide a comprehensive summary of known epigenetic alterations and of the current use of epigenetic drugs for the treatment of hematological malignancies.

摘要

近年来,在血液系统恶性肿瘤患者中已发现表观遗传调节因子的复发性体细胞突变。此外,也有报道称存在染色体易位,其中融合蛋白伴侣本身就是表观遗传调节因子,或者致癌融合蛋白招募/靶向表观遗传调节因子。越来越多的证据表明,“表观遗传药物”可能会给多种血液系统恶性肿瘤带来临床益处,这使得它们被批准用于治疗骨髓增生异常综合征和皮肤T细胞淋巴瘤。大量评估表观遗传药物单药治疗或联合治疗的临床前和临床试验正在进行。本综述的目的是全面总结已知的表观遗传改变以及目前表观遗传药物在治疗血液系统恶性肿瘤中的应用情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/5302993/d5bedc6497cd/oncotarget-07-57327-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/5302993/d5bedc6497cd/oncotarget-07-57327-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/5302993/d5bedc6497cd/oncotarget-07-57327-g001.jpg

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本文引用的文献

1
The safety profile of vorinostat (suberoylanilide hydroxamic acid) in hematologic malignancies: A review of clinical studies.伏立诺他(琥珀酰亚胺基羟肟酸)在血液系统恶性肿瘤中的安全性:临床研究综述。
Cancer Treat Rev. 2016 Feb;43:58-66. doi: 10.1016/j.ctrv.2015.04.003. Epub 2015 Apr 9.
2
An update of current treatments for adult acute myeloid leukemia.成人急性髓系白血病当前治疗方法的最新进展。
Blood. 2016 Jan 7;127(1):53-61. doi: 10.1182/blood-2015-08-604520. Epub 2015 Dec 10.
3
Molecular Pathways: IDH2 Mutations-Co-opting Cellular Metabolism for Malignant Transformation.
Targeting Histone Deacetylases to Modulate Graft-Versus-Host Disease and Graft-Versus-Leukemia.
靶向组蛋白去乙酰化酶调节移植物抗宿主病和移植物抗白血病。
Int J Mol Sci. 2020 Jun 16;21(12):4281. doi: 10.3390/ijms21124281.
4
Frequent upregulation of G9a promotes RelB-dependent proliferation and survival in multiple myeloma.G9a的频繁上调促进了多发性骨髓瘤中RelB依赖性的增殖和存活。
Exp Hematol Oncol. 2020 May 22;9:8. doi: 10.1186/s40164-020-00164-4. eCollection 2020.
5
Hypomethylating Agent Azacitidine Is Effective in Treating Brain Metastasis Triple-Negative Breast Cancer Through Regulation of DNA Methylation of Keratin 18 Gene.低甲基化剂阿扎胞苷通过调节角蛋白18基因的DNA甲基化有效治疗脑转移三阴性乳腺癌。
Transl Oncol. 2020 Jun;13(6):100775. doi: 10.1016/j.tranon.2020.100775. Epub 2020 May 11.
6
Epigenetic-Based Mechanisms of Osteoblast Suppression in Multiple Myeloma Bone Disease.多发性骨髓瘤骨病中基于表观遗传学的成骨细胞抑制机制
JBMR Plus. 2019 Mar 15;3(3):e10183. doi: 10.1002/jbm4.10183. eCollection 2019 Mar.
7
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Nucleic Acids Res. 2018 Nov 2;46(19):10019-10033. doi: 10.1093/nar/gky679.
8
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PLoS Genet. 2018 Jun 7;14(6):e1007362. doi: 10.1371/journal.pgen.1007362. eCollection 2018 Jun.
9
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10
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Clin Cancer Res. 2016 Jan 1;22(1):16-9. doi: 10.1158/1078-0432.CCR-15-0362. Epub 2015 Nov 9.
4
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5
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Clin Cancer Res. 2015 Nov 1;21(21):4767-73. doi: 10.1158/1078-0432.CCR-15-0530. Epub 2015 Sep 11.
6
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J Clin Oncol. 2015 Aug 10;33(23):2492-9. doi: 10.1200/JCO.2014.59.2782. Epub 2015 Jun 22.
9
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Proc Natl Acad Sci U S A. 2015 Mar 10;112(10):E1116-25. doi: 10.1073/pnas.1501199112. Epub 2015 Feb 23.
10
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Br J Haematol. 2015 May;169(4):506-19. doi: 10.1111/bjh.13318. Epub 2015 Feb 23.