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PIWI通路:连接急性髓系白血病干性与细胞分化

PIWI pathway: bridging acute myeloid leukemia stemness and cellular differentiation.

作者信息

Garcia-Silva M R, Márquez M E, Pinello N

机构信息

Functional Genomics Laboratory, Institut Pasteur Montevideo, Montevideo, Uruguay.

出版信息

Front Cell Dev Biol. 2024 Aug 12;12:1449353. doi: 10.3389/fcell.2024.1449353. eCollection 2024.

Abstract

PIWI proteins are stem cell-associated RNA-binding proteins crucial for survival of germ stem cells. In cancer, PIWI proteins are overexpressed. Specifically, PIWIL4 is highly expressed in multiple cancers with the highest levels found in acute myeloid leukemia (AML), an aggressive malignancy propagated by a population of leukemia stem cells (LSCs). Bamezai et al. (Blood Journal, blood, 2023, 142, 90-105) demonstrated that PIWIL4 supports AML blasts and LSCs but is not necessary for healthy human hematopoietic progenitor stem cells (HSPCs) function . PIWIL4 in AML acts by preventing the accumulation of R-loops in key genes for LSCs persistence implicated in: DNA damage, replicative stress, and transcription arrest. We report that PIWIL4 expression significantly decreases in THP-1 monocytes exposed to a differentiating agent, suggesting a potential role for PIWIL4 in maintaining the undifferentiated state of myeloid cells. PIWIL4 overexpression could lead to the emergence of LSCs, driving leukemia propagation and maintenance. Our findings correlate with the persistent overexpression of PIWIL4 in myeloid cancers as reported by Bamezai et al., and suggest that PIWIL4 may be involved in myeloid cell differentiation. In this perspective, we highlight recent findings on the implication of PIWI pathway in maintaining AML stemness. Additionally, we propose further investigation on the role of PIWI pathway in oncogenesis and cellular differentiation as a strategy to identify biomarkers and therapeutic targets for AML.

摘要

PIWI蛋白是与干细胞相关的RNA结合蛋白,对生殖干细胞的存活至关重要。在癌症中,PIWI蛋白过表达。具体而言,PIWIL4在多种癌症中高表达,在急性髓系白血病(AML)中表达水平最高,AML是一种由白血病干细胞(LSC)群体传播的侵袭性恶性肿瘤。Bamezai等人(《血液杂志》,《血液》,2023年,第142卷,第90 - 105页)证明,PIWIL4支持AML原始细胞和LSC,但对健康人类造血祖干细胞(HSPC)的功能不是必需的。AML中的PIWIL4通过防止参与LSC存活的关键基因中R环的积累发挥作用,这些关键基因涉及DNA损伤、复制应激和转录停滞。我们报告,在暴露于分化剂的THP - 1单核细胞中,PIWIL4表达显著降低,这表明PIWIL4在维持髓系细胞未分化状态中可能发挥作用。PIWIL4过表达可能导致LSC出现,驱动白血病的传播和维持。我们的发现与Bamezai等人报道的髓系癌症中PIWIL4的持续过表达相关,并表明PIWIL4可能参与髓系细胞分化。从这个角度来看,我们强调了关于PIWI通路在维持AML干性方面作用的最新发现。此外,我们建议进一步研究PIWI通路在肿瘤发生和细胞分化中的作用,作为识别AML生物标志物和治疗靶点的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4929/11345186/f2a4a4fdf726/fcell-12-1449353-g001.jpg

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