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uPAR放射性核素靶向显像研究进展

Research progress of uPAR-targeted nuclear imaging
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摘要 尿激酶型纤溶酶原激活物及其特异性受体(uPA/uPAR)系统是肿瘤侵袭、转移和血管生成的核心环节之一,且与肿瘤的不良预后密切相关。检测肿瘤组织中uPA/uPAR表达水平及其随病情的变化情况,对于肿瘤预后判断、治疗方案的选择与疗效评价意义重大。放射性核素分子靶向显像方法在靶向受体表达水平测定上具有独特的优势,近来年医学研究者使用多种放射性核素标记uPAR的特异性配体进行了动物显像研究,并于2015年首次用于人体显像。笔者就近年来uPAR放射性核素靶向显像的研究进展作一综述。 Urokinase plasminogen activator (uPA) and urokinase plasminogen activator receptor (uPAR) system play an important role in the process of cancer invasion, metastasis and angiogenesiss, and it is closely associated with poor prognosis of tumors. Evaluate of uPAR expression level in the tumor cell is very significant for cancer prognosis, selection and assement the therapy. Molecular targeted nuclear imaging has unique advantage in testing receptor expression, several research group labeled uPAR specially ligands with different radionuclides for imaging uPAR. The first human uPAR imaging has taken in 2015. This article reviewed the research progress of uPAR-targeted molecular nuclear imaging in recent years.
作者 孙芳芳 张欣
出处 《国际放射医学核医学杂志》 2016年第3期230-234,共5页 International Journal of Radiation Medicine and Nuclear Medicine
基金 辽宁省自然科学基金(2013023017)
关键词 放射性核素显像 尿纤溶酶原激活物 靶向显像 Radionuclide imaging Urinary plasminogen activator Targeted imaging
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参考文献32

  • 1Dass K, Ahmad A, Azmi AS, et al. Evolving role of uPA/uPAR sys- tem in human cancers[J]. Cancer Treat Rev, 2008, 34 (2): 122- 136.
  • 2Noh H, Hong S, Huang S. Role of urokinase receptor in tumor pro- gression and development[J]. Theranostics, 2013, 3 (7): 487-495.
  • 3Dohn LH, Pappot H, Iversen BR, et al. uPAR expression pattern in patients with urothelial carcinoma of the Bladder-Possible clinical implications[J/OL]. PLoS One, 2015, 10(8): e013582412016-01- 05]. http://www, ncbi. nlm. nih. gov/pubmed/26292086.
  • 4Smith HW, Marshall CJ. Regulation of cell signalling by uPAR[J]. Nat Rev Mol Cell Biol, 2010, 11 (1): 23-36.
  • 5Yang J, Duh E J, Caldwell RB, et al. Antipermeability function of PEDF involves blockade of the MAP kinase/GSK/beta-catenin sig- naling pathway and uPAR expression[J]. Invest Ophthalmol Vis Sci, 2010, 51 (6): 3273-3280.
  • 6Messaritou G, East L, Roghi C, et al. Membrane type-1 matrix met- alloproteinase activity is regulated by the endocytic collagen re- ceptor Endol80[J]. J Cell Sci, 2009, 122(Pt 22): 4042-4048.
  • 7Czekay RP, Loskutoff DJ. Plasminogen activator inhibitors regulatecell adhesion through a uPAR-dependent mechanism[J]. J Cell Physiol, 2009, 220(3): 655-663.
  • 8Baldini E, Sorrenti S, D'Armiento E, et al. The urokinase plasmino- gen activating system in thyroid cancer: clinical implications[J]. G Chir, 2012, 33 (10): 305-310.
  • 9Gonias SL, Hu J. Urokinase receptor and resistance to targeted an- ticancer agents[J/OL]. Front Pharmacol, 2015, 6: 15412016-01-05]. http://www, ncbi. nlm. nih. gov/pmc/articles/PMC4515545/.
  • 10Nalla AK, Gorantla B, Gondi CS, et al. Targeting MMP-9, uPAR, and cathepsin B inhibits invasion, migration and acti,ates apoptosis in prostate eancer cells[J]. Cancer Gene Ther, 2010, 17 (9): 599- 613.

二级参考文献18

  • 1Dass K,Ahmad A,Azmi AS. Evolving role of uPA/uPAR system in human cancers[J].{H}Cancer Treatment Reviews,2008.122-136.
  • 2Messaritou G,East L,Roghi C. Membrane type-1 matrix metalloproteinase activity is regulated by the endocytic collagen receptor Endo180[J].{H}Journal of Cell Science,2009,(Pt 22):4042-4048.
  • 3Czekay RP,Loskutoff DJ. Plasminogen activator inhibitors regulate cell adhesion through a uPAR-dependent mechanism[J].{H}Journal of Cellular Physiology,2009.655-663.
  • 4Yang J,Duh E J,Caldwell RB. Antipermeability function of PEDF involves blockade of the MAP kinase/GSK/beta-catenin signaling pathway and uPAR expression[J].{H}Investigative Ophthalmology & Visual Science,2010.3273-3280.
  • 5Smith HW,Marshall CJ. Regulation of cell signalling by uPAR[J].{H}Nature Reviews Molecular Cell Biology,2010.23-36.
  • 6Kntir S,Sato S,Huber T. Development and evaluation of peptidic ligands targeting tumour-associated urokinase plasminogen activator receptor (uPAR) for use in alpha-emitter therapy for disseminated ovarian cancer[J].{H}Europen Journl of Nucler Medicine and Molecular Imging,2008.53-64.
  • 7Gondi CS,Rao JS. Therapeutic potential of siRNA-mediated targeting of urokinase plasminogen activator,its receptor,and matrix metalloproteinases[J].{H}Methods in Molecular Biology,2009.267-281.
  • 8Ahmad A,Kong D,Wang Z. Down-regulation of uPA and uPAR by 3,3'-diindolylmethane contributes to the inhibition of cell growth and migration of breast cancer cells[J].{H}Journal of Cellular Biochemistry,2009.916-925.
  • 9Ulisse S,Baldini E,Sorrenti S. The urokinase plasminogen activator system:a target for anti-cancer therapy[J].{H}CURRENT CANCER DRUG TARGETS,2009.32-71.
  • 10Nalla AK,Gorantla B,Gondi CS. Targeting MMP-9,uPAR,and cathepsin B inhibits invasion,migration and activates apoptosis in prostate cancer cells[J].{H}Cancer Gene Therapy,2010.599-613.

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