Paediatric bone marrow mesenchymal stem cells support acute myeloid leukaemia cell survival and enhance chemoresistance via contact-independent mechanism.

IF 5.1 2区 医学 Q1 HEMATOLOGY British Journal of Haematology Pub Date : 2024-11-10 DOI:10.1111/bjh.19884
Alison Laing, Ahmed Elmarghany, Arwa A Alghaith, Aya Gouma, Thomas Stevens, Alexander Winton, Jennifer Cassels, Cassie J Clarke, Claire Schwab, Christine J Harrison, Brenda Gibson, Karen Keeshan
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引用次数: 0

Abstract

Children diagnosed with acute myeloid leukaemia (paediatric AML [pAML]) have limited treatment options and relapse rates due to chemoresistance and refractory disease are over 30%. Current treatment is cytotoxic and in itself has long-lasting harsh side effects. New, less toxic treatments are needed. The bone marrow microenvironment provides chemoprotection to leukaemic cells through cell communication and interaction with mesenchymal stem cells (MSCs), but this is not well defined in pAML. Using primary patient material, we identify a cell contact-independent mechanism of MSC-mediated chemoprotection involving extrinsic soluble factors that is abrogated through inhibition of the JAK/STAT and ERK pathways.

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小儿骨髓间充质干细胞通过接触无关机制支持急性髓性白血病细胞存活并增强化疗抵抗力。
被诊断出患有急性髓性白血病(儿科急性髓性白血病 [pAML])的儿童可选择的治疗方法有限,因化疗耐药性和难治性疾病导致的复发率超过 30%。目前的治疗方法是细胞毒疗法,其本身具有长期的严重副作用。我们需要毒性较低的新疗法。骨髓微环境通过细胞通讯和与间充质干细胞(MSCs)的相互作用为白血病细胞提供化学保护,但这在pAML中还没有得到很好的定义。我们利用原发患者材料,确定了间充质干细胞介导的化学保护机制,该机制与细胞接触无关,涉及外在可溶性因子,通过抑制JAK/STAT和ERK通路可抑制该机制。
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
期刊最新文献
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