• 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

使用CXCR4靶向磁性荧光纳米探针单芯片分离耐药急性髓系白血病细胞

One-Chip Isolation of Drug-Resistant Acute Myeloid Leukemia Cells with CXCR4-Targeted Magnetic Fluorescent Nanoprobes.

作者信息

Wang Fan, Jiang Yuqi, Wang Luhai, Chen Yi, Zhang Yu, Ma Ming

机构信息

State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Sciences and Medical Engineering, Southeast University, Nanjing 210096, China.

出版信息

Nanomaterials (Basel). 2022 May 17;12(10):1711. doi: 10.3390/nano12101711.

DOI:10.3390/nano12101711
PMID:35630929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9142899/
Abstract

Drug resistance and relapse lead to high mortality in acute myeloid leukemia, and studies have shown that CXCR4 overexpression is highly correlated with poor prognosis and drug resistance in leukemia cells. Isolation and detection of AML cells with CXCR4 overexpression will be crucial to the treatment of AML. In this paper, magnetic nanoparticles were firstly prepared successfully by high-temperature thermal decomposition method, and then characterized by TEM, VSM and DLS. Subsequently CXCR4-targeted magnetic fluorescent nanoprobes conjugated with antibody 12G5 were constructed by stepwise coupling. In cell experiments, the obtained probes demonstrated excellent targeting efficacy to CXCR4 overexpressed AML cells HL-60. In addition, HL-60 cells labelled with the magnetic probes can be magnetic isolated successfully in one microfluidics chip, with efficiency of 82.92 ± 7.03%. Overall, this method utilizes the superiority of superparamagnetic nanomaterials and microfluidic technology to achieve the enrichment and capture of drug-resistant cells in a microfluidic chip, providing a new idea for the isolation and detective of drug-resistant acute myeloid leukemia cells.

摘要

耐药性和复发导致急性髓系白血病的高死亡率,研究表明CXCR4过表达与白血病细胞的不良预后和耐药性高度相关。分离和检测CXCR4过表达的急性髓系白血病细胞对急性髓系白血病的治疗至关重要。本文首先通过高温热分解法成功制备了磁性纳米颗粒,然后通过透射电子显微镜、振动样品磁强计和动态光散射对其进行了表征。随后,通过逐步偶联构建了与抗体12G5偶联的CXCR4靶向磁性荧光纳米探针。在细胞实验中,所获得的探针显示出对CXCR4过表达的急性髓系白血病细胞HL-60具有优异的靶向效果。此外,用磁性探针标记的HL-60细胞能够在一个微流控芯片中成功地进行磁性分离,分离效率为82.92±7.03%。总体而言,该方法利用超顺磁性纳米材料和微流控技术的优势,在微流控芯片中实现耐药细胞的富集和捕获,为耐药急性髓系白血病细胞的分离和检测提供了新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/8d836ca5000e/nanomaterials-12-01711-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/f32999926f57/nanomaterials-12-01711-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/7f3e290a41ae/nanomaterials-12-01711-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/30d17c5113d2/nanomaterials-12-01711-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/df014f985994/nanomaterials-12-01711-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/2862452175ce/nanomaterials-12-01711-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/4111eeb1f574/nanomaterials-12-01711-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/9a071c05b44e/nanomaterials-12-01711-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/5ca0b7797efb/nanomaterials-12-01711-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/8d836ca5000e/nanomaterials-12-01711-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/f32999926f57/nanomaterials-12-01711-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/7f3e290a41ae/nanomaterials-12-01711-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/30d17c5113d2/nanomaterials-12-01711-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/df014f985994/nanomaterials-12-01711-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/2862452175ce/nanomaterials-12-01711-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/4111eeb1f574/nanomaterials-12-01711-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/9a071c05b44e/nanomaterials-12-01711-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/5ca0b7797efb/nanomaterials-12-01711-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6181/9142899/8d836ca5000e/nanomaterials-12-01711-g008.jpg

相似文献

1
One-Chip Isolation of Drug-Resistant Acute Myeloid Leukemia Cells with CXCR4-Targeted Magnetic Fluorescent Nanoprobes.使用CXCR4靶向磁性荧光纳米探针单芯片分离耐药急性髓系白血病细胞
Nanomaterials (Basel). 2022 May 17;12(10):1711. doi: 10.3390/nano12101711.
2
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.
3
Label-free microfluidic chip for segregation and recovery of circulating leukemia cells: clinical applications in acute myeloid leukemia.用于循环白血病细胞分离和回收的无标记微流控芯片:在急性髓系白血病中的临床应用
Biomed Microdevices. 2023 Dec 12;26(1):3. doi: 10.1007/s10544-023-00687-7.
4
Antineoplastic effect of a diphtheria toxin-based nanoparticle targeting acute myeloid leukemia cells overexpressing CXCR4.基于白喉毒素的纳米颗粒对过表达 CXCR4 的急性髓系白血病细胞的抗肿瘤作用。
J Control Release. 2021 Jul 10;335:117-129. doi: 10.1016/j.jconrel.2021.05.014. Epub 2021 May 15.
5
CXCR4 Overexpression is a Poor Prognostic Factor in Pediatric Acute Myeloid Leukemia With Low Risk: A Report From the Japanese Pediatric Leukemia/Lymphoma Study Group.CXCR4过表达是低危小儿急性髓系白血病的不良预后因素:来自日本小儿白血病/淋巴瘤研究组的报告
Pediatr Blood Cancer. 2016 Aug;63(8):1394-9. doi: 10.1002/pbc.26035. Epub 2016 May 2.
6
MiR-9 functions as a tumor suppressor in acute myeloid leukemia by targeting CX chemokine receptor 4.微小RNA-9通过靶向CXC趋化因子受体4在急性髓系白血病中发挥肿瘤抑制作用。
Am J Transl Res. 2019 Jun 15;11(6):3384-3397. eCollection 2019.
7
Long non-coding RNA MALAT1 modulate cell migration, proliferation and apoptosis by sponging microRNA-146a to regulate CXCR4 expression in acute myeloid leukemia.长链非编码 RNA MALAT1 通过海绵吸附 microRNA-146a 调节 CXCR4 表达来调节急性髓系白血病中的细胞迁移、增殖和凋亡。
Hematology. 2021 Dec;26(1):43-52. doi: 10.1080/16078454.2020.1867781.
8
CXCR4-mediated signaling regulates autophagy and influences acute myeloid leukemia cell survival and drug resistance.CXCR4 介导的信号转导调节自噬,影响急性髓系白血病细胞的存活和耐药性。
Cancer Lett. 2018 Jul 1;425:1-12. doi: 10.1016/j.canlet.2018.03.024. Epub 2018 Mar 21.
9
The FLT3-ITD mutation and the expression of its downstream signaling intermediates STAT5 and Pim-1 are positively correlated with CXCR4 expression in patients with acute myeloid leukemia.FLT3-ITD 突变及其下游信号转导介质 STAT5 和 Pim-1 的表达与急性髓系白血病患者的 CXCR4 表达呈正相关。
Sci Rep. 2019 Aug 21;9(1):12209. doi: 10.1038/s41598-019-48687-z.
10
Targeting primary acute myeloid leukemia with a new CXCR4 antagonist IgG1 antibody (PF-06747143).针对原发性急性髓细胞白血病的新型 CXCR4 拮抗剂 IgG1 抗体(PF-06747143)。
Sci Rep. 2017 Aug 4;7(1):7305. doi: 10.1038/s41598-017-07848-8.

引用本文的文献

1
Comprehensive analysis of immune-related lncRNAs in AML patients uncovers potential therapeutic targets and prognostic biomarkers.对急性髓系白血病(AML)患者免疫相关长链非编码RNA(lncRNA)的综合分析揭示了潜在的治疗靶点和预后生物标志物。
Heliyon. 2024 May 7;10(9):e30616. doi: 10.1016/j.heliyon.2024.e30616. eCollection 2024 May 15.
2
Current and Emerging Techniques for Diagnosis and MRD Detection in AML: A Comprehensive Narrative Review.急性髓系白血病诊断及微小残留病检测的当前及新兴技术:一篇全面的叙述性综述
Cancers (Basel). 2023 Feb 21;15(5):1362. doi: 10.3390/cancers15051362.

本文引用的文献

1
Cancer statistics, 2022.癌症统计数据,2022 年。
CA Cancer J Clin. 2022 Jan;72(1):7-33. doi: 10.3322/caac.21708. Epub 2022 Jan 12.
2
Biomarker barcodes: multiplexed microfluidic immunohistochemistry enables high-throughput analysis of tissue microarray.生物标志物条码:多重微流控免疫组化使组织微阵列的高通量分析成为可能。
Lab Chip. 2021 Sep 14;21(18):3471-3482. doi: 10.1039/d1lc00375e.
3
Leukemia stem cell-bone marrow microenvironment interplay in acute myeloid leukemia development.急性髓系白血病发展过程中白血病干细胞与骨髓微环境的相互作用
Exp Hematol Oncol. 2021 Jul 10;10(1):39. doi: 10.1186/s40164-021-00233-2.
4
Flow cytometry: principles, applications and recent advances.流式细胞术:原理、应用及最新进展。
Bioanalysis. 2021 Feb;13(3):181-198. doi: 10.4155/bio-2020-0267. Epub 2021 Feb 5.
5
Design, synthesis, and evaluation of pyrrolidine based CXCR4 antagonists with in vivo anti-tumor metastatic activity.基于吡咯烷的具有体内抗肿瘤转移活性的CXCR4拮抗剂的设计、合成与评价。
Eur J Med Chem. 2020 Nov 1;205:112537. doi: 10.1016/j.ejmech.2020.112537. Epub 2020 Jul 23.
6
Circulating Tumor Cells Detection in Patients with Early Breast Cancer Using MACS Immunomagnetic Flow Cytometry.利用MACS免疫磁珠流式细胞术检测早期乳腺癌患者循环肿瘤细胞
Avicenna J Med Biotechnol. 2020 Jul-Sep;12(3):148-156.
7
CXCR4-Targeted PET Imaging of Central Nervous System B-Cell Lymphoma.CXCR4 靶向 PET 成像在中枢神经系统 B 细胞淋巴瘤中的应用。
J Nucl Med. 2020 Dec;61(12):1765-1771. doi: 10.2967/jnumed.120.241703. Epub 2020 Apr 24.
8
Significance of CXCL12/CXCR4 Ligand/Receptor Axis in Various Aspects of Acute Myeloid Leukemia.CXCL12/CXCR4配体/受体轴在急性髓系白血病各方面的意义
Cancer Manag Res. 2020 Mar 24;12:2155-2165. doi: 10.2147/CMAR.S234883. eCollection 2020.
9
The Importance of Poly(ethylene glycol) Alternatives for Overcoming PEG Immunogenicity in Drug Delivery and Bioconjugation.聚乙二醇替代物在克服药物递送和生物偶联中聚乙二醇免疫原性方面的重要性。
Polymers (Basel). 2020 Feb 2;12(2):298. doi: 10.3390/polym12020298.
10
Expression Profile Screening and Bioinformatics Analysis of circRNA, LncRNA, and mRNA in Acute Myeloid Leukemia Drug-Resistant Cells.急性髓系白血病耐药细胞中 circRNA、lncRNA 和 mRNA 的表达谱筛选及生物信息学分析。
Turk J Haematol. 2020 May 6;37(2):104-110. doi: 10.4274/tjh.galenos.2019.2019.0312. Epub 2019 Dec 10.