Epigenomic machinery regulating pediatric AML: Clonal expansion mechanisms, therapies, and future perspectives

IF 12.1 1区 医学 Q1 ONCOLOGY Seminars in cancer biology Pub Date : 2023-07-01 DOI:10.1016/j.semcancer.2023.03.009
Ugo Chianese , Chiara Papulino , Wout Megchelenbrink , Francesco Paolo Tambaro , Fortunato Ciardiello , Rosaria Benedetti , Lucia Altucci
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Abstract

Acute myeloid leukemia (AML) is a heterogeneous disease with a genetic, epigenetic, and transcriptional etiology mainly presenting somatic and germline abnormalities. AML incidence rises with age but can also occur during childhood. Pediatric AML (pAML) accounts for 15–20% of all pediatric leukemias and differs considerably from adult AML. Next-generation sequencing technologies have enabled the research community to “paint” the genomic and epigenomic landscape in order to identify pathology-associated mutations and other prognostic biomarkers in pAML. Although current treatments have improved the prognosis for pAML, chemoresistance, recurrence, and refractory disease remain major challenges. In particular, pAML relapse is commonly caused by leukemia stem cells that resist therapy. Marked patient-to-patient heterogeneity is likely the primary reason why the same treatment is successful for some patients but, at best, only partially effective for others. Accumulating evidence indicates that patient-specific clonal composition impinges significantly on cellular processes, such as gene regulation and metabolism. Although our understanding of metabolism in pAML is still in its infancy, greater insights into these processes and their (epigenetic) modulation may pave the way toward novel treatment options. In this review, we summarize current knowledge on the function of genetic and epigenetic (mis)regulation in pAML, including metabolic features observed in the disease. Specifically, we describe how (epi)genetic machinery can affect chromatin status during hematopoiesis, leading to an altered metabolic profile, and focus on the potential value of targeting epigenetic abnormalities in precision and combination therapy for pAML. We also discuss the possibility of using alternative epidrug-based therapeutic approaches that are already in clinical practice, either alone as adjuvant treatments and/or in combination with other drugs.

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调节儿童AML的表观基因组机制:克隆扩增机制、疗法和未来展望
急性粒细胞白血病(AML)是一种异质性疾病,其病因包括遗传、表观遗传和转录,主要表现为体细胞和种系异常。AML的发病率随着年龄的增长而上升,但也可能发生在儿童时期。儿童AML(pAML)占所有儿童白血病的15-20%,与成人AML有很大不同。下一代测序技术使研究界能够“描绘”基因组和表观基因组景观,以识别pAML中的病理学相关突变和其他预后生物标志物。尽管目前的治疗已经改善了pAML的预后,但化疗耐药性、复发和难治性疾病仍然是主要的挑战。特别是,pAML复发通常是由白血病干细胞抵抗治疗引起的。显著的患者间异质性可能是相同治疗对某些患者成功,但对其他患者充其量只能部分有效的主要原因。越来越多的证据表明,患者特异性克隆组成显著影响细胞过程,如基因调节和代谢。尽管我们对pAML代谢的理解仍处于初级阶段,但对这些过程及其(表观遗传学)调节的深入了解可能会为新的治疗选择铺平道路。在这篇综述中,我们总结了目前关于pAML中遗传和表观遗传学(mis)调节功能的知识,包括在该疾病中观察到的代谢特征。具体而言,我们描述了(epi)遗传机制如何影响造血过程中的染色质状态,导致代谢谱的改变,并重点关注靶向表观遗传异常在pAML精准治疗和联合治疗中的潜在价值。我们还讨论了使用已经在临床实践中的替代表观药物治疗方法的可能性,无论是单独作为辅助治疗还是与其他药物联合使用。
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来源期刊
Seminars in cancer biology
Seminars in cancer biology 医学-肿瘤学
CiteScore
26.80
自引率
4.10%
发文量
347
审稿时长
15.1 weeks
期刊介绍: Seminars in Cancer Biology (YSCBI) is a specialized review journal that focuses on the field of molecular oncology. Its primary objective is to keep scientists up-to-date with the latest developments in this field. The journal adopts a thematic approach, dedicating each issue to an important topic of interest to cancer biologists. These topics cover a range of research areas, including the underlying genetic and molecular causes of cellular transformation and cancer, as well as the molecular basis of potential therapies. To ensure the highest quality and expertise, every issue is supervised by a guest editor or editors who are internationally recognized experts in the respective field. Each issue features approximately eight to twelve authoritative invited reviews that cover various aspects of the chosen subject area. The ultimate goal of each issue of YSCBI is to offer a cohesive, easily comprehensible, and engaging overview of the selected topic. The journal strives to provide scientists with a coordinated and lively examination of the latest developments in the field of molecular oncology.
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