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本文引用的文献

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Biochem Pharmacol. 2020 Dec;182:114253. doi: 10.1016/j.bcp.2020.114253. Epub 2020 Oct 2.
2
DNA Methylation-Based Epigenetic Repression of SLC22A4 Promotes Resistance to Cytarabine in Acute Myeloid Leukemia.基于 DNA 甲基化的 SLC22A4 表观遗传抑制促进急性髓系白血病对阿糖胞苷的耐药性。
Clin Transl Sci. 2021 Jan;14(1):137-142. doi: 10.1111/cts.12861. Epub 2020 Sep 9.
3
Insights on the Interplay between Cells Metabolism and Signaling: A Therapeutic Perspective in Pediatric Acute Leukemias.细胞代谢与信号转导相互作用的研究进展:小儿急性白血病的治疗策略。
Int J Mol Sci. 2020 Aug 28;21(17):6251. doi: 10.3390/ijms21176251.
4
Quantitative proteomics reveals specific metabolic features of acute myeloid leukemia stem cells.定量蛋白质组学揭示了急性髓系白血病干细胞的特定代谢特征。
Blood. 2020 Sep 24;136(13):1507-1519. doi: 10.1182/blood.2019003654.
5
Aldehyde dehydrogenase 3a2 protects AML cells from oxidative death and the synthetic lethality of ferroptosis inducers.醛脱氢酶 3A2 可保护 AML 细胞免受氧化死亡和铁死亡诱导剂的合成致死作用。
Blood. 2020 Sep 10;136(11):1303-1316. doi: 10.1182/blood.2019001808.
6
Metabolomics in acute myeloid leukemia.代谢组学在急性髓系白血病中的应用。
Mol Genet Metab. 2020 Aug;130(4):230-238. doi: 10.1016/j.ymgme.2020.05.005. Epub 2020 May 18.
7
A Bump in the Road: How the Hostile AML Microenvironment Affects CAR T Cell Therapy.道路上的障碍:恶性急性髓系白血病微环境如何影响嵌合抗原受体T细胞疗法
Front Oncol. 2020 Feb 28;10:262. doi: 10.3389/fonc.2020.00262. eCollection 2020.
8
New and Emerging Targeted Therapies for Pediatric Acute Myeloid Leukemia (AML).小儿急性髓系白血病(AML)的新型及新兴靶向治疗方法
Children (Basel). 2020 Feb 10;7(2):12. doi: 10.3390/children7020012.
9
Advances in Pediatric Acute Promyelocytic Leukemia.儿童急性早幼粒细胞白血病的进展
Children (Basel). 2020 Feb 2;7(2):11. doi: 10.3390/children7020011.
10
An update on the molecular pathogenesis and potential therapeutic targeting of AML with t(8;21)(q22;q22.1);RUNX1-RUNX1T1.AML 伴 t(8;21)(q22;q22.1);RUNX1-RUNX1T1 的分子发病机制及潜在治疗靶点的研究进展。
Blood Adv. 2020 Jan 14;4(1):229-238. doi: 10.1182/bloodadvances.2019000168.

从分子和代谢角度对儿童急性髓系白血病可靶向特征的叙述性综述。

Narrative review of targetable features of pediatric acute myeloid leukemia from molecular and metabolic perspectives.

作者信息

Trabal Adriana Milagros, Chandra Joya

机构信息

Division of Pediatric Oncology and Patient Care, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Pediatr Med. 2021 Feb 28;4. doi: 10.21037/pm-20-98.

DOI:10.21037/pm-20-98
PMID:39877586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11774499/
Abstract

BACKGROUND AND OBJECTIVE

Unlike the majority of pediatric leukemia patients, young patients with acute myeloid leukemia (AML) have not seen significant improvement in treatment outcomes. This is frequently attributed to the heterogeneity of this malignancy in terms of its mutations and molecularly defined categories. In adult versus pediatric cases of AML, the heterogeneity is preserved, although there are key differences in the incidence of gene mutations, chromosomal translocations, and other molecular features. Current treatment strategies consider broader cellular features of AML, such as altered metabolic and anti-apoptotic properties, and many of these are common across pediatric and adult AML.

METHODS

A narrative review was conducted to compile literature regarding molecular and metabolic features of AML and new treatment modalities in the adult and pediatric population. Articles published in PubMed were gathered and studied over 6 months for review and comparison. Studies published in English over a ten-year period from 2000-2020 were included. Keywords used for the searches included acute myeloid leukemia, cytogenetics, pediatric acute myeloid leukemia, and treatment of acute myeloid leukemia.

KEY CONTENT AND FINDINGS

Molecular characteristics of adult-onset myeloid leukemia as compared to those in the pediatric population are detailed. We highlight unique features of pediatric AML biology and potential ties to metabolism, as well as recent advances in therapy.

CONCLUSIONS

Differences in adult and pediatric AML cytogenetics, metabolism, and molecular features should be further characterized in order to individualize treatment, develop new therapeutic options, and improve patient outcome.

摘要

背景与目的

与大多数小儿白血病患者不同,急性髓系白血病(AML)的年轻患者治疗结局并未得到显著改善。这通常归因于这种恶性肿瘤在突变和分子定义类别方面的异质性。在成人与小儿AML病例中,尽管基因突变、染色体易位及其他分子特征的发生率存在关键差异,但异质性依然存在。当前的治疗策略考虑了AML更广泛的细胞特征,如代谢改变和抗凋亡特性,其中许多在小儿和成人AML中是共有的。

方法

进行了一项叙述性综述,以汇编有关成人和小儿人群中AML的分子和代谢特征以及新治疗方式的文献。收集并研究了在PubMed上发表超过6个月的文章以供综述和比较。纳入了2000年至2020年十年间以英文发表的研究。搜索使用的关键词包括急性髓系白血病、细胞遗传学、小儿急性髓系白血病以及急性髓系白血病的治疗。

关键内容与发现

详细阐述了成人起病的髓系白血病与小儿人群相比的分子特征。我们强调了小儿AML生物学的独特特征及其与代谢的潜在联系,以及治疗方面的最新进展。

结论

应进一步明确成人和小儿AML在细胞遗传学、代谢和分子特征方面的差异,以便实现个体化治疗、开发新的治疗选择并改善患者结局。