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Thermoacoustic molecular tomography with magnetic nanoparticle contrast agents for targeted tumor detection.基于磁性纳米颗粒对比剂的热声分子断层成像用于靶向肿瘤检测。
Med Phys. 2010 Aug;37(8):4193-200. doi: 10.1118/1.3466696.
2
Proliferating macrophages associated with high grade, hormone receptor negative breast cancer and poor clinical outcome.与高级别、激素受体阴性乳腺癌和不良临床结局相关的增殖巨噬细胞。
Breast Cancer Res Treat. 2011 Aug;128(3):703-711. doi: 10.1007/s10549-010-1154-y. Epub 2010 Sep 15.
3
Gold nanoparticles cellular toxicity and recovery: effect of size, concentration and exposure time.金纳米颗粒的细胞毒性及其恢复:粒径、浓度和暴露时间的影响。
Nanotoxicology. 2010 Mar;4(1):120-37. doi: 10.3109/17435390903471463.
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Optical imaging and magnetic field targeting of magnetic nanoparticles in tumors.肿瘤中磁性纳米粒子的光学成像和磁场靶向。
ACS Nano. 2010 Sep 28;4(9):5217-24. doi: 10.1021/nn101427t.
5
Zinc oxide nanoparticles for selective destruction of tumor cells and potential for drug delivery applications.氧化锌纳米颗粒用于选择性破坏肿瘤细胞和药物输送应用的潜力。
Expert Opin Drug Deliv. 2010 Sep;7(9):1063-77. doi: 10.1517/17425247.2010.502560.
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The promotion of human malignant melanoma growth by mesoporous silica nanoparticles through decreased reactive oxygen species.介孔二氧化硅纳米颗粒通过降低活性氧促进人类恶性黑色素瘤生长。
Biomaterials. 2010 Aug;31(24):6142-53. doi: 10.1016/j.biomaterials.2010.04.055. Epub 2010 May 26.
7
Enhanced cytotoxicity and activation of ROS-dependent c-Jun NH2-terminal kinase and caspase-3 by low doses of tetrandrine-loaded nanoparticles in Lovo cells--a possible Trojan strategy against cancer.载纳米双氢青蒿素对 Lovo 细胞的低剂量增敏作用及其机制:一种潜在的肿瘤治疗策略。
Eur J Pharm Biopharm. 2010 Aug;75(3):334-40. doi: 10.1016/j.ejpb.2010.04.016. Epub 2010 May 11.
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Lipid coated mesoporous silica nanoparticles as photosensitive drug carriers.脂质包覆的介孔硅纳米粒子作为光敏药物载体。
Phys Chem Chem Phys. 2010 May 7;12(17):4418-22. doi: 10.1039/b924370d. Epub 2010 Feb 24.
9
Ratio of M2 macrophage expression is closely associated with poor prognosis for Angioimmunoblastic T-cell lymphoma (AITL).M2 巨噬细胞表达的比例与血管免疫母细胞性 T 细胞淋巴瘤(AITL)的不良预后密切相关。
Pathol Int. 2010 Apr;60(4):278-83. doi: 10.1111/j.1440-1827.2010.02514.x.
10
Manipulation of iron transporter genes results in the suppression of human and mouse mammary adenocarcinomas.操纵铁转运蛋白基因可抑制人源和鼠源乳腺腺癌。
Anticancer Res. 2010 Mar;30(3):759-65.

肿瘤消融与纳米技术。

Tumor ablation and nanotechnology.

机构信息

Department of Biomedical Engineering, Lerner Research Institute, and Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.

出版信息

Mol Pharm. 2010 Dec 6;7(6):1880-98. doi: 10.1021/mp1001944. Epub 2010 Oct 7.

DOI:10.1021/mp1001944
PMID:20866097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2997921/
Abstract

Next to surgical resection, tumor ablation is a commonly used intervention in the treatment of solid tumors. Tumor ablation methods include thermal therapies, photodynamic therapy, and reactive oxygen species (ROS) producing agents. Thermal therapies induce tumor cell death via thermal energy and include radiofrequency, microwave, high intensity focused ultrasound, and cryoablation. Photodynamic therapy and ROS producing agents cause increased oxidative stress in tumor cells leading to apoptosis. While these therapies are safe and viable alternatives when resection of malignancies is not feasible, they do have associated limitations that prevent their widespread use in clinical applications. To improve the efficacy of these treatments, nanoparticles are being studied in combination with nonsurgical ablation regimens. In addition to better thermal effect on tumor ablation, nanoparticles can deliver anticancer therapeutics that show a synergistic antitumor effect in the presence of heat and can also be imaged to achieve precision in therapy. Understanding the molecular mechanism of nanoparticle-mediated tumor ablation could further help engineer nanoparticles of appropriate composition and properties to synergize the ablation effect. This review aims to explore the various types of nonsurgical tumor ablation methods currently used in cancer treatment and potential improvements by nanotechnology applications.

摘要

除了手术切除,肿瘤消融是治疗实体瘤的常用干预手段。肿瘤消融方法包括热疗、光动力疗法和活性氧(ROS)产生剂。热疗通过热能诱导肿瘤细胞死亡,包括射频、微波、高强度聚焦超声和冷冻消融。光动力疗法和 ROS 产生剂导致肿瘤细胞中氧化应激增加,从而导致细胞凋亡。虽然这些疗法在无法进行恶性肿瘤切除时是安全可行的替代方法,但它们确实存在相关限制,阻碍了它们在临床应用中的广泛使用。为了提高这些治疗方法的疗效,正在研究纳米颗粒与非手术消融方案联合使用。除了在肿瘤消融方面有更好的热效应外,纳米颗粒还可以输送抗癌药物,在热的存在下表现出协同抗肿瘤作用,并且还可以进行成像,以实现治疗的精确性。了解纳米颗粒介导的肿瘤消融的分子机制可能有助于进一步设计具有适当组成和性质的纳米颗粒,以协同消融效果。本综述旨在探讨目前用于癌症治疗的各种非手术肿瘤消融方法以及纳米技术应用的潜在改进。