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蛙皮素受体介导的成像和细胞毒性:综述与现状。

Bombesin receptor-mediated imaging and cytotoxicity: review and current status.

机构信息

Digestive Diseases Branch, National Institutes of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Curr Drug Deliv. 2011 Jan;8(1):79-134. doi: 10.2174/156720111793663624.


DOI:10.2174/156720111793663624
PMID:21034419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3058932/
Abstract

The three mammalian bombesin (Bn) receptors (gastrin-releasing peptide [GRP] receptor, neuromedin B [NMB] receptor, BRS-3) are one of the classes of G protein-coupled receptors that are most frequently over-express/ectopically expressed by common, important malignancies. Because of the clinical success of somatostatin receptor-mediated imaging and cytotoxicity with neuroendocrine tumors, there is now increasing interest in pursuing a similar approach with Bn receptors. In the last few years then have been more than 200 studies in this area. In the present paper, the in vitro and in vivo results, as well as results of human studies from many of these studies are reviewed and the current state of Bn receptor-mediated imaging or cytotoxicity is discussed. Both Bn receptor-mediated imaging studies as well as Bn receptor-mediated tumoral cytotoxic studies using radioactive and non-radioactive Bn-based ligands are covered.

摘要

三种哺乳动物脑肠肽(Bn)受体(胃泌素释放肽[GRP]受体、神经介素 B[NMB]受体、BRS-3)是 G 蛋白偶联受体中最常过度表达/异位表达的一类,常见于重要的恶性肿瘤。由于生长抑素受体介导的神经内分泌肿瘤成像和细胞毒性的临床成功,现在人们越来越有兴趣采用类似的方法研究 Bn 受体。在过去的几年中,该领域已经进行了 200 多项研究。本文综述了这些研究中的体外和体内结果,以及来自许多人类研究的结果,并讨论了 Bn 受体介导的成像或细胞毒性的现状。本文涵盖了 Bn 受体介导的放射性和非放射性基于 Bn 的配体成像研究以及 Bn 受体介导的肿瘤细胞毒性研究。

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本文引用的文献

[1]
Neuromedin B receptors regulate EGF receptor tyrosine phosphorylation in lung cancer cells.

Eur J Pharmacol. 2010-4-11

[2]
A standardised study to compare prostate cancer targeting efficacy of five radiolabelled bombesin analogues.

Eur J Nucl Med Mol Imaging. 2010-2-25

[3]
Evaluation of [99mTc-(CO)3-X-Y-Bombesin(7-14)NH2] conjugates for targeting gastrin-releasing peptide receptors overexpressed on breast carcinoma.

Anticancer Res. 2010-1

[4]
Selective apoptotic killing of solid and hematologic tumor cells by bombesin-targeted delivery of mitochondria-disrupting peptides.

Mol Pharm. 2010-4-5

[5]
Tetraamine-derived bifunctional chelators for technetium-99m labelling: synthesis, bioconjugation and evaluation as targeted SPECT imaging probes for GRP-receptor-positive tumours.

Chemistry. 2010-2-15

[6]
Versatile new bis(thiosemicarbazone) bifunctional chelators: synthesis, conjugation to bombesin(7-14)-NH(2), and copper-64 radiolabeling.

Inorg Chem. 2010-2-15

[7]
Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

Bioconjug Chem. 2009-12

[8]
177Lu-AMBA biodistribution, radiotherapeutic efficacy, imaging, and autoradiography in prostate cancer models with low GRP-R expression.

J Nucl Med. 2009-12

[9]
Receptor-binding, biodistribution, dosimetry, and micro-SPECT/CT imaging of 111In-[DTPA(1), Lys(3), Tyr(4)]-bombesin analog in human prostate tumor-bearing mice.

Cancer Biother Radiopharm. 2009-8

[10]
Evaluation of a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-conjugated bombesin-based radioantagonist for the labeling with single-photon emission computed tomography, positron emission tomography, and therapeutic radionuclides.

Clin Cancer Res. 2009-8-15

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