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本文引用的文献

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Bioluminescence and MR Imaging of the Safety and Efficacy of Vascular Disruption in Gliomas.胶质瘤中血管破坏安全性和有效性的生物发光与磁共振成像
Mol Imaging Biol. 2016 Dec;18(6):860-869. doi: 10.1007/s11307-016-0963-8.
2
Comparative Analysis of Matrix Metalloproteinase Family Members Reveals That MMP9 Predicts Survival and Response to Temozolomide in Patients with Primary Glioblastoma.基质金属蛋白酶家族成员的比较分析表明,MMP9可预测原发性胶质母细胞瘤患者的生存期及对替莫唑胺的反应。
PLoS One. 2016 Mar 29;11(3):e0151815. doi: 10.1371/journal.pone.0151815. eCollection 2016.
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Inhibition of MMP14 potentiates the therapeutic effect of temozolomide and radiation in gliomas.抑制 MMP14 可增强替莫唑胺和放疗在脑胶质瘤中的治疗效果。
Cancer Med. 2013 Aug;2(4):457-67. doi: 10.1002/cam4.104. Epub 2013 Jun 30.
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Assessment of efficacy of antifungals against Aspergillus fumigatus: value of real-time bioluminescence imaging.评估抗真菌药物对烟曲霉的疗效:实时生物发光成像的价值。
Antimicrob Agents Chemother. 2013 Jul;57(7):3046-59. doi: 10.1128/AAC.01660-12. Epub 2013 Apr 15.
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Real-time bioluminescence and tomographic imaging of gastric cancer in a novel orthotopic mouse model.新型原位小鼠胃癌模型中实时生物发光和断层成像技术的应用。
Oncol Rep. 2012 Jun;27(6):1937-43. doi: 10.3892/or.2012.1713. Epub 2012 Mar 7.
6
Downregulation of Akt and FAK phosphorylation reduces invasion of glioblastoma cells by impairment of MT1-MMP shuttling to lamellipodia and downregulates MMPs expression.Akt和FAK磷酸化的下调通过损害MT1-MMP向丝状伪足的穿梭而减少胶质母细胞瘤细胞的侵袭,并下调MMPs的表达。
Biochim Biophys Acta. 2011 May;1813(5):655-67. doi: 10.1016/j.bbamcr.2011.01.020. Epub 2011 Jan 26.
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J Biol Chem. 2010 Dec 17;285(51):40201-11. doi: 10.1074/jbc.M110.147330. Epub 2010 Oct 11.
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Exciting new advances in neuro-oncology: the avenue to a cure for malignant glioma.神经肿瘤学的激动人心新进展:攻克恶性脑胶质瘤的途径。
CA Cancer J Clin. 2010 May-Jun;60(3):166-93. doi: 10.3322/caac.20069.
9
Tissue inhibitor of metalloproteinase-3 expression from an oncolytic adenovirus inhibits matrix metalloproteinase activity in vivo without affecting antitumor efficacy in malignant glioma.来自溶瘤腺病毒的金属蛋白酶组织抑制剂-3表达可在体内抑制基质金属蛋白酶活性,而不影响对恶性胶质瘤的抗肿瘤疗效。
Cancer Res. 2005 Oct 15;65(20):9398-405. doi: 10.1158/0008-5472.CAN-04-4264.
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Looking and listening to light: the evolution of whole-body photonic imaging.观察与聆听光线:全身光子成像的发展历程
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通过基质金属蛋白酶(MMP)表达的分子成像预测替莫唑胺的抗胶质瘤治疗效果。

Prediction of the anti-glioma therapeutic effects of temozolomide through molecular imaging of MMP expression.

作者信息

Li Li, Du Yang, Xiang Dehui, Chen Liang, Shi Zhifeng, Tian Jie, Chen Xinjian

机构信息

School of Electronic and Information Engineering, Soochow University, No. 1 Ten Azusa Street, Suzhou, 215006, China.

State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Soochow University, Suzhou, 215123, China.

出版信息

Biomed Opt Express. 2018 Jun 20;9(7):3193-3207. doi: 10.1364/BOE.9.003193. eCollection 2018 Jul 1.

DOI:10.1364/BOE.9.003193
PMID:29984093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6033562/
Abstract

Currently, there is no effective way to assess the therapeutic response of temozolomide (TMZ) for the glioma. In this study, the human U87MG-fLuc glioma animal models were set up and the antitumor efficacy of TMZ was evaluated using bioluminescence imaging (BLI) and MRI. Then, bioluminescence tomography (BLT) was reconstructed using an adaptive sparsity matching pursuit (ASMP) algorithm. Second, the expression level of the MMP-750 probe was examined with or without TMZ treatment using FMI. Third, the expression of MMP2 and MMP3 was specifically examined after treatment. The results showed that TMZ effectively inhibited glioma growth. The targeted imaging of MMP-750 was decreased during the treatment of glioma with TMZ. Moreover, the MMP2 and MMP3 expression was found to correlate with the inhibition effect of TMZ. Our study indicated that the therapeutic effects of TMZ can be effectively evaluated at an early stage using molecular imaging, and MMP targeting the fluorescence probe could be utilized for the prediction and assessment of the therapeutic effects of TMZ.

摘要

目前,尚无有效的方法来评估替莫唑胺(TMZ)对胶质瘤的治疗反应。在本研究中,建立了人U87MG-fLuc胶质瘤动物模型,并使用生物发光成像(BLI)和磁共振成像(MRI)评估了TMZ的抗肿瘤疗效。然后,使用自适应稀疏匹配追踪(ASMP)算法重建生物发光断层扫描(BLT)。其次,使用荧光分子成像(FMI)检测有无TMZ治疗时MMP-750探针的表达水平。第三,在治疗后特异性检测MMP2和MMP3的表达。结果显示,TMZ有效抑制了胶质瘤生长。在用TMZ治疗胶质瘤期间,MMP-750的靶向成像降低。此外,发现MMP2和MMP3的表达与TMZ的抑制作用相关。我们的研究表明,使用分子成像可在早期有效评估TMZ的治疗效果,且靶向MMP的荧光探针可用于预测和评估TMZ的治疗效果。