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骨髓增生异常综合征和急性髓系白血病中的干细胞:近亲还是无关实体?

Stem Cells in Myelodysplastic Syndromes and Acute Myeloid Leukemia: First Cousins or Unrelated Entities?

作者信息

Joudinaud Romane, Boyer Thomas

机构信息

Laboratory of Hematology, Lille Hospital, Lille, France.

Laboratory of Hematology, University of Amiens, Amiens Hospital, Amiens, France.

出版信息

Front Oncol. 2021 Aug 20;11:730899. doi: 10.3389/fonc.2021.730899. eCollection 2021.

Abstract

Myelodysplastic syndromes (MDSs) are associated with a significant risk of transformation to acute myeloid leukemia (AML), supported by alterations affecting malignant stem cells. This review focuses on the metabolic, phenotypic and genetic characteristics underlying this dynamic evolution, from myelodysplastic stem cells (MDS-SCs) to leukemic stem cells (LSCs). MDS-SCs are more likely to be derived from healthy hematopoietic stem cells (HSCs), whereas LSCs may originate from healthy progenitors, mostly LMPP (lymphoid-primed multipotential progenitors). Moreover, overexpression of CD123 and CLL1 markers by LSCs and MDS-SCs in high risk-MDS [HR-MDS] has led to exciting therapeutic applications. Single-cell sequencing has suggested that clonal evolution in the stem cell compartment was non-linear during MDS initiation and progression to AML, with pre-MDS-SC acquiring distinct additional mutations in parallel, that drive either MDS blast production or AML transformation. In AML and HR-MDS, common metabolic alterations have been identified in malignant stem cells, including activation of the protein machinery and dependence on oxidative phosphorylation. Targeting these metabolic abnormalities could prevent HR-MDS from progressing to AML. Strikingly, in low risk-MDS-SC, the expression of ribosomal proteins is decreased, which may be accompanied by a reduction in protein synthesis.

摘要

骨髓增生异常综合征(MDS)与转化为急性髓系白血病(AML)的显著风险相关,这一过程受到影响恶性干细胞的改变的支持。本综述聚焦于从骨髓增生异常干细胞(MDS-SC)到白血病干细胞(LSC)这一动态演变过程背后的代谢、表型和遗传特征。MDS-SC更有可能源自健康的造血干细胞(HSC),而LSC可能起源于健康的祖细胞,主要是淋巴系定向多能祖细胞(LMPP)。此外,LSC和MDS-SC在高危MDS(HR-MDS)中CD123和CLL1标志物的过表达已带来了令人兴奋的治疗应用。单细胞测序表明,在MDS起始及进展为AML的过程中,干细胞区室中的克隆进化是非线性的,前MDS-SC会同时获得不同的额外突变,这些突变驱动MDS原始细胞生成或AML转化。在AML和HR-MDS中,已在恶性干细胞中鉴定出常见的代谢改变,包括蛋白质机制的激活和对氧化磷酸化的依赖。针对这些代谢异常可能会阻止HR-MDS进展为AML。引人注目的是,在低危MDS-SC中,核糖体蛋白的表达降低,这可能伴随着蛋白质合成的减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8af6/8417738/f9733212d8a0/fonc-11-730899-g001.jpg

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