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本文引用的文献

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Controlling toxicity of Peptide-drug conjugates by different chemical linker structures.通过不同化学连接子结构控制肽-药物偶联物的毒性
ChemMedChem. 2015 May;10(5):804-14. doi: 10.1002/cmdc.201402514. Epub 2015 Apr 9.
2
Synthesis and in vitro and in vivo evaluation of an (18)F-labeled neuropeptide Y analogue for imaging of breast cancer by PET.一种用于正电子发射断层显像(PET)乳腺癌成像的(18)F标记神经肽Y类似物的合成及其体外和体内评价
Mol Pharm. 2015 Apr 6;12(4):1121-30. doi: 10.1021/mp500601z. Epub 2015 Mar 13.
3
Drug delivery and release systems for targeted tumor therapy.用于靶向肿瘤治疗的药物递送与释放系统。
J Pept Sci. 2015 Mar;21(3):186-200. doi: 10.1002/psc.2753. Epub 2015 Feb 23.
4
Neuropeptide Y Y1 receptors mediate [corrected] targeted delivery of anticancer drug with encapsulated nanoparticles to breast cancer cells with high selectivity and its potential for breast cancer therapy.神经肽Y Y1受体介导[已修正]用包封纳米颗粒将抗癌药物靶向递送至乳腺癌细胞,具有高选择性及其在乳腺癌治疗中的潜力。
ACS Appl Mater Interfaces. 2015 Mar 11;7(9):5574-82. doi: 10.1021/acsami.5b00270. Epub 2015 Feb 26.
5
Receptor-mediated uptake of boron-rich neuropeptide y analogues for boron neutron capture therapy.用于硼中子俘获治疗的富含硼的神经肽Y类似物的受体介导摄取。
ChemMedChem. 2015 Jan;10(1):164-72. doi: 10.1002/cmdc.201402368. Epub 2014 Oct 22.
6
Nanotechnology and tumor microcirculation.纳米技术与肿瘤微循环。
Adv Drug Deliv Rev. 2014 Jul;74:2-11. doi: 10.1016/j.addr.2013.08.010. Epub 2013 Aug 30.
7
Neuropeptide Y receptors: how to get subtype selectivity.神经肽 Y 受体:如何获得亚型选择性。
Front Endocrinol (Lausanne). 2013 Feb 4;4:5. doi: 10.3389/fendo.2013.00005. eCollection 2013.
8
Heterobivalent dual-target probe for targeting GRP and Y1 receptors on tumor cells.用于针对肿瘤细胞上的 GRP 和 Y1 受体的异价双靶探针。
Bioorg Med Chem Lett. 2013 Feb 1;23(3):687-92. doi: 10.1016/j.bmcl.2012.11.110. Epub 2012 Dec 5.
9
High expression of NPY receptors in the human testis.人睾丸中 NPY 受体的高表达。
Mol Cell Endocrinol. 2011 Apr 30;337(1-2):62-70. doi: 10.1016/j.mce.2011.01.021. Epub 2011 Feb 2.
10
Ligand-induced internalization and recycling of the human neuropeptide Y2 receptor is regulated by its carboxyl-terminal tail.配体诱导的人神经肽 Y2 受体的内化和再循环受其羧基末端尾部调节。
J Biol Chem. 2010 Dec 31;285(53):41578-90. doi: 10.1074/jbc.M110.162156. Epub 2010 Oct 18.

神经肽 Y 受体:癌症成像和治疗的有前途的靶点。

Neuropeptide Y receptors: a promising target for cancer imaging and therapy.

机构信息

Key Laboratory of Magnetic Materials and Devices & Division of Functional Materials and Nano Devices, Ningbo Institute of Materials Technology & Engineering, Chinese Academy of Sciences, Ningbo 315201, China.

出版信息

Regen Biomater. 2015 Sep;2(3):215-9. doi: 10.1093/rb/rbv013. Epub 2015 Aug 7.

DOI:10.1093/rb/rbv013
PMID:26816643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4669009/
Abstract

Neuropeptide Y (NPY) was first identified from porcine brain in 1982, and plays its biological functions in humans through NPY receptors (Y1, Y2, Y4 and Y5). NPY receptors are known to mediate various physiological functions and involve in a majority of human diseases, such as obesity, hypertension, epilepsy and metabolic disorders. Recently, NPY receptors have been found to be overexpressed in many cancers, so they emerged as promising target in cancer diagnosis and therapy. This review focuses on the latest research about NPY and NPY receptors, and summarizes the current knowledge on NPY receptors expression in cancers, selective ligands for NPY receptors and their application in cancer imaging and therapy.

摘要

神经肽 Y(NPY)于 1982 年首次从猪脑中被鉴定出来,通过 NPY 受体(Y1、Y2、Y4 和 Y5)在人体内发挥其生物学功能。已知 NPY 受体介导各种生理功能,并涉及大多数人类疾病,如肥胖、高血压、癫痫和代谢紊乱。最近,人们发现 NPY 受体在许多癌症中过度表达,因此它们成为癌症诊断和治疗有前途的靶点。本综述重点介绍了 NPY 和 NPY 受体的最新研究进展,总结了 NPY 受体在癌症中的表达、NPY 受体的选择性配体及其在癌症成像和治疗中的应用的现有知识。