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高三尖杉酯碱治疗急性髓系白血病的研究进展。

Homoharringtonine in the treatment of acute myeloid leukemia: A review.

机构信息

The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, P.R. China.

Department of Clinical Hematology and Transfusion, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, P.R. China.

出版信息

Medicine (Baltimore). 2024 Nov 1;103(44):e40380. doi: 10.1097/MD.0000000000040380.

DOI:10.1097/MD.0000000000040380
PMID:39496012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11537654/
Abstract

Acute myeloid leukemia (AML) is a hematological malignancy characterized by the accumulation of immature myeloid precursor cells. Over half of AML patients fail to achieve long-term disease-free survival under existing therapy, and the overall prognosis is poor, necessitating the urgent development of novel therapeutic approaches. The plant alkaloid homoharringtonine (HHT), which has anticancer properties, was first identified more than 40 years ago. It works in a novel method of action that prevents the early elongation phase of protein synthesis. HHT has been widely utilized in the treatment of AML, with strong therapeutic effects, few toxic side effects, and the ability to enhance AML patients' prognoses. In AML, HHT can induce cell apoptosis through multiple pathways, exerting synergistic antitumor effects, according to clinical and pharmacological research. About its modes of action, some findings have been made recently. This paper reviews the development of research on the mechanisms of HHT in treating AML to offer insights for further research and clinical therapy.

摘要

急性髓系白血病(AML)是一种血液系统恶性肿瘤,其特征是不成熟的髓系前体细胞的积累。超过一半的 AML 患者在现有治疗下无法实现长期无病生存,整体预后较差,因此迫切需要开发新的治疗方法。植物生物碱高三尖杉酯碱(HHT)具有抗癌特性,它在 40 多年前首次被发现。它的作用机制是阻止蛋白质合成的早期延伸阶段。HHT 已广泛应用于 AML 的治疗,具有较强的治疗效果、较少的毒副作用,并能改善 AML 患者的预后。在 AML 中,HHT 可以通过多种途径诱导细胞凋亡,根据临床和药理学研究,发挥协同抗肿瘤作用。关于其作用机制,最近有了一些发现。本文综述了 HHT 治疗 AML 的作用机制研究进展,为进一步的研究和临床治疗提供思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/fbb9d0d58f26/medi-103-e40380-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/9e1c81de5a21/medi-103-e40380-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/b6d8801ae06b/medi-103-e40380-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/e1c18549f462/medi-103-e40380-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/4e0878b5e9c2/medi-103-e40380-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/fbb9d0d58f26/medi-103-e40380-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/9e1c81de5a21/medi-103-e40380-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/b6d8801ae06b/medi-103-e40380-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/e1c18549f462/medi-103-e40380-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/4e0878b5e9c2/medi-103-e40380-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d612/11537654/fbb9d0d58f26/medi-103-e40380-g005.jpg

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本文引用的文献

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Acute Myeloid Leukemia, Version 3.2023, NCCN Clinical Practice Guidelines in Oncology.急性髓系白血病,第 3 版 2023 年,NCCN 肿瘤学临床实践指南。
J Natl Compr Canc Netw. 2023 May;21(5):503-513. doi: 10.6004/jnccn.2023.0025.
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Acute myeloid leukaemia.急性髓细胞白血病。
Lancet. 2023 Jun 17;401(10393):2073-2086. doi: 10.1016/S0140-6736(23)00108-3. Epub 2023 Apr 15.
3
Spermatogenesis associated serine rich 2 like plays a prognostic factor and therapeutic target in acute myeloid leukemia by regulating the JAK2/STAT3/STAT5 axis.
丝氨酸丰富的精原细胞瘤相关蛋白 2 样通过调控 JAK2/STAT3/STAT5 轴在急性髓系白血病中发挥预后因子和治疗靶点的作用。
J Transl Med. 2023 Feb 11;21(1):115. doi: 10.1186/s12967-023-03968-0.
4
Dihydropyrimidinase-like 2 can serve as a novel therapeutic target and prognostic biomarker in acute myeloid leukemia.二氢嘧啶酶样 2 可作为急性髓系白血病的新型治疗靶点和预后生物标志物。
Cancer Med. 2023 Apr;12(7):8319-8330. doi: 10.1002/cam4.5531. Epub 2023 Jan 9.
5
Homoharringtonine is synergistically lethal with BCL-2 inhibitor APG-2575 in acute myeloid leukemia.高三尖杉酯碱与 BCL-2 抑制剂 APG-2575 在急性髓系白血病中具有协同致死作用。
J Transl Med. 2022 Jul 6;20(1):299. doi: 10.1186/s12967-022-03497-2.
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The Metabolic Signature of AML Cells Treated With Homoharringtonine.高三尖杉酯碱处理的急性髓系白血病细胞的代谢特征
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