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老药新用:I 型干扰素治疗急性髓系白血病。

Old Dog, New Trick: Type I IFN-Based Treatment for Acute Myeloid Leukemia.

机构信息

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, England, United Kingdom.

MRC Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, England, United Kingdom.

出版信息

Mol Cancer Res. 2021 May;19(5):753-756. doi: 10.1158/1541-7786.MCR-20-0871. Epub 2021 Jan 26.

DOI:10.1158/1541-7786.MCR-20-0871
PMID:33500358
Abstract

Despite strong biological rationale for the use of type-I IFNs for the treatment of acute myeloid leukemia (AML), their usage is limited to few hematologic malignancies. Here, we propose that innate immune sensing machinery, particularly the stimulator of IFN genes pathway, may be exploited to deliver antileukemic effects in AML.

摘要

尽管 I 型干扰素(IFNs)在治疗急性髓系白血病(AML)方面具有强有力的生物学理论基础,但它们的应用仅限于少数血液恶性肿瘤。在这里,我们提出先天免疫感应机制,特别是干扰素基因刺激途径,可用于在 AML 中发挥抗白血病作用。

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Mol Cancer Res. 2021 May;19(5):753-756. doi: 10.1158/1541-7786.MCR-20-0871. Epub 2021 Jan 26.
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引用本文的文献

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Cancer Gene Ther. 2025 Apr;32(4):475-485. doi: 10.1038/s41417-025-00888-7. Epub 2025 Mar 19.
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TLR3 agonism augments CD47 inhibition in acute myeloid leukemia.TLR3 激动剂增强急性髓系白血病中的 CD47 抑制作用。
Haematologica. 2024 Jul 1;109(7):2111-2121. doi: 10.3324/haematol.2023.283850.
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SHR1032, a novel STING agonist, stimulates anti-tumor immunity and directly induces AML apoptosis.
SHR1032,一种新型的 STING 激动剂,能刺激抗肿瘤免疫并直接诱导 AML 细胞凋亡。
Sci Rep. 2022 May 20;12(1):8579. doi: 10.1038/s41598-022-12449-1.
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Recent Progress in Interferon Therapy for Myeloid Malignancies.骨髓恶性肿瘤干扰素治疗的最新进展
Front Oncol. 2021 Oct 29;11:769628. doi: 10.3389/fonc.2021.769628. eCollection 2021.