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RUNX1和CBFB改变在急性髓系白血病及其他血液系统疾病中的临床相关性

Clinical Relevance of RUNX1 and CBFB Alterations in Acute Myeloid Leukemia and Other Hematological Disorders.

作者信息

Metzeler Klaus H, Bloomfield Clara D

机构信息

Laboratory for Leukemia Diagnostics, Department of Internal Medicine III, University of Munich, Munich, Germany.

The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.

出版信息

Adv Exp Med Biol. 2017;962:175-199. doi: 10.1007/978-981-10-3233-2_12.

DOI:10.1007/978-981-10-3233-2_12
PMID:28299658
Abstract

The translocation t(8;21), leading to a fusion between the RUNX1 gene and the RUNX1T1 locus, was the first chromosomal translocation identified in cancer. Since the first description of this balanced rearrangement in a patient with acute myeloid leukemia (AML) in 1973, RUNX1 translocations and point mutations have been found in various myeloid and lymphoid neoplasms. In this chapter, we summarize the currently available data on the clinical relevance of core binding factor gene alterations in hematological disorders. In the first section, we discuss the prognostic implications of the core binding factor translocations RUNX1-RUNX1T1 and CBFB-MYH11 in AML patients. We provide an overview of the cooperating genetic events in patients with CBF-rearranged AML and their clinical implications, and review current treatment approaches for CBF AML and the utility of minimal residual disease monitoring. In the next sections, we summarize the available data on rare RUNX1 rearrangements in various hematologic neoplasms and the role of RUNX1 translocations in therapy-related myeloid neoplasia. The final three sections of the chapter cover the spectrum and clinical significance of RUNX1 point mutations in AML and myelodysplastic syndromes, in familial platelet disorder with associated myeloid malignancy, and in acute lymphoblastic leukemia.

摘要

导致RUNX1基因与RUNX1T1基因座融合的8号和21号染色体易位,是在癌症中发现的首例染色体易位。自1973年在一名急性髓系白血病(AML)患者中首次描述这种平衡重排以来,在各种髓系和淋巴系肿瘤中均发现了RUNX1易位和点突变。在本章中,我们总结了目前关于核心结合因子基因改变在血液系统疾病中的临床相关性的可用数据。在第一节中,我们讨论了核心结合因子易位RUNX1-RUNX1T1和CBFB-MYH11在AML患者中的预后意义。我们概述了CBF重排AML患者中协同发生的遗传事件及其临床意义,并回顾了CBF AML的当前治疗方法以及微小残留病监测的效用。在接下来的部分中,我们总结了各种血液系统肿瘤中罕见RUNX1重排的可用数据以及RUNX1易位在治疗相关髓系肿瘤中的作用。本章的最后三节涵盖了RUNX1点突变在AML和骨髓增生异常综合征、伴有相关髓系恶性肿瘤的家族性血小板疾病以及急性淋巴细胞白血病中的范围和临床意义。

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Ann Hematol. 2025 Aug 11. doi: 10.1007/s00277-025-06545-1.
2
Efficacy of novel agents against cellular models of familial platelet disorder with myeloid malignancy (FPD-MM).新型药物对伴有髓系恶性肿瘤的家族性血小板疾病(FPD-MM)细胞模型的疗效。
Blood Cancer J. 2024 Feb 5;14(1):25. doi: 10.1038/s41408-024-00981-4.
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Outcome and prognostic factors of CBF pediatric AML patients with t(8;21) differ from patients with inv(16).
CBF 儿科 AML 伴 t(8;21)患者的预后因素和结果与 inv(16)患者不同。
BMC Cancer. 2023 May 25;23(1):476. doi: 10.1186/s12885-023-10965-5.
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Genome-wide CRISPR screens identify ferroptosis as a novel therapeutic vulnerability in acute lymphoblastic leukemia.全基因组 CRISPR 筛选鉴定铁死亡为急性淋巴细胞白血病的一种新的治疗靶点。
Haematologica. 2023 Feb 1;108(2):382-393. doi: 10.3324/haematol.2022.280786.
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Is a Novel Translocation Partner of via t(2;16)(q37;q22) in Acute Myeloid Leukemia.在急性髓系白血病中, 是通过 t(2;16)(q37;q22) 与 的新型易位伙伴。
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