• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

近红外氧化磷酸化抑制剂整合急性髓系白血病靶向成像与治疗。

Near-infrared oxidative phosphorylation inhibitor integrates acute myeloid leukemia-targeted imaging and therapy.

机构信息

Institute of Rocket Force Medicine, State Key Laboratory of Trauma, Burns and Combined Injury, College of Preventive Medicine, Third Military Medical University (Army Medical University), Chongqing 400038, China.

Department of Hematology, Xinqiao Hospital, Third Military Medical University (Army Medical University), Chongqing 400037, China.

出版信息

Sci Adv. 2021 Jan 1;7(1). doi: 10.1126/sciadv.abb6104. Print 2021 Jan.

DOI:10.1126/sciadv.abb6104
PMID:33523835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7775779/
Abstract

Acute myeloid leukemia (AML) is a deadly hematological malignancy with frequent disease relapse. The biggest challenge for AML therapy is the lack of methods to target and kill the heterogeneous leukemia cells, which lead to disease relapse. Here, we describe a near-infrared (NIR) fluorescent dye, IR-26, which preferentially accumulates in the mitochondria of AML cells, depending on the hyperactive glycolysis of malignant cell, and simultaneously impairs oxidative phosphorylation (OXPHOS) to exert targeted therapeutic effects for AML cells. In particular, IR-26 also exhibits potential for real-time monitoring of AML cells with an in vivo flow cytometry (IVFC) system. Therefore, IR-26 represents a novel all-in-one agent for the integration of AML targeting, detection, and therapy, which may help to monitor disease progression and treatment responses, prevent unnecessary delays in administering upfront therapy, and improve therapeutic efficiency to the residual AML cells, which are responsible for disease relapse.

摘要

急性髓系白血病(AML)是一种致命的血液系统恶性肿瘤,常伴有疾病复发。AML 治疗的最大挑战是缺乏靶向和杀伤异质性白血病细胞的方法,这导致疾病复发。在这里,我们描述了一种近红外(NIR)荧光染料 IR-26,它依赖于恶性细胞的过度活跃糖酵解,优先积聚在 AML 细胞的线粒体中,同时损害氧化磷酸化(OXPHOS),以发挥针对 AML 细胞的靶向治疗作用。特别是,IR-26 还可以通过体内流式细胞术(IVFC)系统实时监测 AML 细胞。因此,IR-26 代表了一种新型的 AML 靶向、检测和治疗一体化的试剂,它可能有助于监测疾病进展和治疗反应,防止不必要地延迟进行一线治疗,并提高对负责疾病复发的残留 AML 细胞的治疗效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/8c0c007c2d20/abb6104-F6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/05b8b3ff66d3/abb6104-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/5669fc91fd8f/abb6104-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/433a27d53b27/abb6104-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/3136e4ed000c/abb6104-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/3db5a2754ee6/abb6104-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/8c0c007c2d20/abb6104-F6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/05b8b3ff66d3/abb6104-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/5669fc91fd8f/abb6104-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/433a27d53b27/abb6104-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/3136e4ed000c/abb6104-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/3db5a2754ee6/abb6104-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/7775779/8c0c007c2d20/abb6104-F6.jpg

相似文献

1
Near-infrared oxidative phosphorylation inhibitor integrates acute myeloid leukemia-targeted imaging and therapy.近红外氧化磷酸化抑制剂整合急性髓系白血病靶向成像与治疗。
Sci Adv. 2021 Jan 1;7(1). doi: 10.1126/sciadv.abb6104. Print 2021 Jan.
2
Mitochondrial metabolism: powering new directions in acute myeloid leukemia.线粒体代谢:为急性髓系白血病的新方向提供动力。
Leuk Lymphoma. 2021 Oct;62(10):2331-2341. doi: 10.1080/10428194.2021.1910685. Epub 2021 Jun 1.
3
The thymidine dideoxynucleoside analog, alovudine, inhibits the mitochondrial DNA polymerase γ, impairs oxidative phosphorylation and promotes monocytic differentiation in acute myeloid leukemia.胸腺嘧啶脱氧核苷类似物阿昔洛韦能抑制线粒体 DNA 聚合酶 γ,损害氧化磷酸化,并促进急性髓系白血病中的单核细胞分化。
Haematologica. 2019 May;104(5):963-972. doi: 10.3324/haematol.2018.195172. Epub 2018 Dec 20.
4
Targeting mitochondrial RNA polymerase in acute myeloid leukemia.靶向急性髓系白血病中的线粒体RNA聚合酶。
Oncotarget. 2015 Nov 10;6(35):37216-28. doi: 10.18632/oncotarget.6129.
5
Acute myeloid leukemia sensitivity to metabolic inhibitors: glycolysis showed to be a better therapeutic target.急性髓细胞白血病对代谢抑制剂的敏感性:糖酵解被证明是更好的治疗靶点。
Med Oncol. 2020 Jul 28;37(8):72. doi: 10.1007/s12032-020-01394-6.
6
Targeting the metabolic vulnerability of acute myeloid leukemia blasts with a combination of venetoclax and 8-chloro-adenosine.联合 venetoclax 和 8-氯腺苷靶向急性髓系白血病原始细胞的代谢脆弱性。
J Hematol Oncol. 2021 Apr 26;14(1):70. doi: 10.1186/s13045-021-01076-4.
7
Targeting mitochondrial respiration for the treatment of acute myeloid leukemia.针对线粒体呼吸治疗急性髓系白血病。
Biochem Pharmacol. 2020 Dec;182:114253. doi: 10.1016/j.bcp.2020.114253. Epub 2020 Oct 2.
8
Adrenomedullin-CALCRL axis controls relapse-initiating drug tolerant acute myeloid leukemia cells.肾上腺髓质素-CALCRL 轴控制复发起始的药物耐受急性髓系白血病细胞。
Nat Commun. 2021 Jan 18;12(1):422. doi: 10.1038/s41467-020-20717-9.
9
An Auristatin nanoconjugate targeting CXCR4+ leukemic cells blocks acute myeloid leukemia dissemination.靶向 CXCR4+白血病细胞的 Auristatin 纳米偶联物阻断急性髓系白血病的扩散。
J Hematol Oncol. 2020 Apr 15;13(1):36. doi: 10.1186/s13045-020-00863-9.
10
Mitochondrial metabolism as a potential therapeutic target in myeloid leukaemia.线粒体代谢作为髓系白血病的潜在治疗靶点。
Leukemia. 2022 Jan;36(1):1-12. doi: 10.1038/s41375-021-01416-w. Epub 2021 Sep 24.

引用本文的文献

1
Feasibility and Safety of Targeting Mitochondria Function and Metabolism in Acute Myeloid Leukemia.靶向急性髓系白血病线粒体功能和代谢的可行性与安全性
Curr Pharmacol Rep. 2024 Dec;10(6):388-404. doi: 10.1007/s40495-024-00378-8. Epub 2024 Oct 4.
2
A Phthalimide-Functionalized Heptamethine Cyanine Dye for Tumor-Targeted Photothermal Therapy.一种用于肿瘤靶向光热治疗的邻苯二甲酰亚胺功能化七甲川花菁染料。
Cancers (Basel). 2024 Dec 13;16(24):4155. doi: 10.3390/cancers16244155.
3
Targeting protein tyrosine phosphatase non-receptor type 6 (PTPN6) as a therapeutic strategy in acute myeloid leukemia.

本文引用的文献

1
Nucleophosmin1 (NPM1) abnormality in hematologic malignancies, and therapeutic targeting of mutant NPM1 in acute myeloid leukemia.血液系统恶性肿瘤中的核磷蛋白1(NPM1)异常以及急性髓系白血病中突变型NPM1的治疗靶点
Ther Adv Hematol. 2020 Feb 3;11:2040620719899818. doi: 10.1177/2040620719899818. eCollection 2020.
2
The leukaemia stem cell: similarities, differences and clinical prospects in CML and AML.白血病干细胞:CML 和 AML 中的相似性、差异性和临床前景。
Nat Rev Cancer. 2020 Mar;20(3):158-173. doi: 10.1038/s41568-019-0230-9. Epub 2020 Jan 6.
3
Metabolic dependencies and vulnerabilities in leukemia.
靶向蛋白酪氨酸磷酸酶非受体6型(PTPN6)作为急性髓系白血病的一种治疗策略。
Cell Biol Toxicol. 2024 Dec 21;41(1):11. doi: 10.1007/s10565-024-09965-3.
4
Dysfunction of astrocytic glycophagy exacerbates reperfusion injury in ischemic stroke.星形胶质细胞糖酵解功能障碍加剧缺血性脑卒中再灌注损伤。
Redox Biol. 2024 Aug;74:103234. doi: 10.1016/j.redox.2024.103234. Epub 2024 Jun 7.
5
Mitochondria Energy Metabolism Depression as Novel Adjuvant to Sensitize Radiotherapy and Inhibit Radiation Induced-Pulmonary Fibrosis.线粒体能量代谢抑制作为增敏放疗和抑制放射性肺纤维化的新辅助手段。
Adv Sci (Weinh). 2024 Jul;11(26):e2401394. doi: 10.1002/advs.202401394. Epub 2024 May 7.
6
Unimolecular Self-Assembled Hemicyanine-Oleic Acid Conjugate Acts as a Novel Succinate Dehydrogenase Inhibitor to Amplify Photodynamic Therapy and Eliminate Cancer Stem Cells.单分子自组装半菁-油酸共轭物作为一种新型琥珀酸脱氢酶抑制剂,可增强光动力疗法并消除癌症干细胞。
Research (Wash D C). 2023 Sep 6;6:0223. doi: 10.34133/research.0223. eCollection 2023.
7
Recent Metal Nanotheranostics for Cancer Diagnosis and Therapy: A Review.近期用于癌症诊断与治疗的金属纳米诊疗学:综述
Diagnostics (Basel). 2023 Feb 22;13(5):833. doi: 10.3390/diagnostics13050833.
8
supports mitochondrial dynamics and immune evasion to CD8 T cell in lung adenocarcinoma.支持肺腺癌中 CD8 T 细胞的线粒体动力学和免疫逃逸。
PeerJ. 2022 Dec 21;10:e14543. doi: 10.7717/peerj.14543. eCollection 2022.
9
Affinity probes based on small-molecule inhibitors for tumor imaging.基于小分子抑制剂的亲和探针用于肿瘤成像。
Front Oncol. 2022 Oct 27;12:1028493. doi: 10.3389/fonc.2022.1028493. eCollection 2022.
10
Cascade two-stage tumor re-oxygenation and immune re-sensitization mediated by self-assembled albumin-sorafenib nanoparticles for enhanced photodynamic immunotherapy.自组装白蛋白-索拉非尼纳米颗粒介导的级联双阶段肿瘤再氧合和免疫再敏化用于增强光动力免疫治疗
Acta Pharm Sin B. 2022 Nov;12(11):4204-4223. doi: 10.1016/j.apsb.2022.07.023. Epub 2022 Aug 8.
白血病中的代谢依赖性和脆弱性。
Genes Dev. 2019 Nov 1;33(21-22):1460-1474. doi: 10.1101/gad.326470.119.
4
Oxidative phosphorylation as a potential therapeutic target for cancer therapy.氧化磷酸化作为癌症治疗的潜在治疗靶点。
Int J Cancer. 2020 Jan 1;146(1):10-17. doi: 10.1002/ijc.32616. Epub 2019 Sep 11.
5
Mubritinib Targets the Electron Transport Chain Complex I and Reveals the Landscape of OXPHOS Dependency in Acute Myeloid Leukemia.Mubritinib 靶向电子传递链复合物 I,并揭示急性髓系白血病中氧化磷酸化依赖性的全景。
Cancer Cell. 2019 Jul 8;36(1):84-99.e8. doi: 10.1016/j.ccell.2019.06.003.
6
Metabolic reprogramming toward oxidative phosphorylation identifies a therapeutic target for mantle cell lymphoma.向氧化磷酸化代谢重编程鉴定出治疗套细胞淋巴瘤的一个治疗靶点。
Sci Transl Med. 2019 May 8;11(491). doi: 10.1126/scitranslmed.aau1167.
7
Gboxin is an oxidative phosphorylation inhibitor that targets glioblastoma.Gboxin 是一种靶向神经胶质瘤的氧化磷酸化抑制剂。
Nature. 2019 Mar;567(7748):341-346. doi: 10.1038/s41586-019-0993-x. Epub 2019 Mar 6.
8
Genetic Hierarchy of Acute Myeloid Leukemia: From Clonal Hematopoiesis to Molecular Residual Disease.急性髓系白血病的遗传层次:从克隆性造血到分子残留病。
Int J Mol Sci. 2018 Dec 3;19(12):3850. doi: 10.3390/ijms19123850.
9
Identification of Chemotherapy-Induced Leukemic-Regenerating Cells Reveals a Transient Vulnerability of Human AML Recurrence.鉴定化疗诱导的白血病再生细胞揭示了人类 AML 复发的短暂脆弱性。
Cancer Cell. 2018 Sep 10;34(3):483-498.e5. doi: 10.1016/j.ccell.2018.08.007.
10
An NIR-Fluorophore-Based Therapeutic Endoplasmic Reticulum Stress Inducer.一种基于近红外荧光团的内质网应激诱导治疗剂。
Adv Mater. 2018 Jul 1:e1800475. doi: 10.1002/adma.201800475.