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抗肿瘤剂杯芳烃 0118 作为糖结合的别构抑制剂,以人半乳糖凝集素-1 为靶点。

Antitumor agent calixarene 0118 targets human galectin-1 as an allosteric inhibitor of carbohydrate binding.

机构信息

Department of Biochemistry, Molecular Biology & Biophysics, University of Minnesota Health Sciences Center, 6-155 Jackson Hall, 321 Church Street, Minneapolis, Minnesota 55455, United States.

出版信息

J Med Chem. 2012 Jun 14;55(11):5121-9. doi: 10.1021/jm300014q. Epub 2012 May 30.

Abstract

Calix[4]arene compound 0118 is an angiostatic agent that inhibits tumor growth in mice. Although 0118 is a topomimetic of galectin-1-targeting angiostatic amphipathic peptide Anginex, we had yet to prove that 0118 targets galectin-1. Galectin-1 is involved in pathological disorders like tumor endothelial cell adhesion and migration and therefore presents a relevant target for therapeutic intervention against cancer. Here, (15)N-(1)H HSQC NMR spectroscopy demonstrates that 0118 indeed targets galectin-1 at a site away from the lectin's carbohydrate binding site and thereby attenuates lactose binding to the lectin. Flow cytometry and agglutination assays show that 0118 attenuates binding of galectin-1 to cell surface glycans, and the inhibition of cell proliferation by 0118 is found to be correlated with the cellular expression of the lectin. In general, our data indicate that 0118 targets galectin-1 as an allosteric inhibitor of glycan/carbohydrate binding. This work contributes to the clinical development of antitumor calixarene compound 0118.

摘要

冠醚化合物 0118 是一种血管生成抑制剂,可抑制小鼠肿瘤生长。虽然 0118 是靶向半乳糖凝集素-1 的血管生成两亲肽 Anginex 的拟态物,但我们尚未证明 0118 靶向半乳糖凝集素-1。半乳糖凝集素-1 参与肿瘤内皮细胞黏附和迁移等病理紊乱,因此是治疗癌症的相关靶点。在这里,(15)N-(1)H HSQC NMR 光谱表明,0118 确实在远离凝集素碳水化合物结合位点的部位靶向半乳糖凝集素-1,从而减弱乳糖与凝集素的结合。流式细胞术和凝集试验表明,0118 减弱了半乳糖凝集素-1与细胞表面糖链的结合,并且发现 0118 抑制细胞增殖与该凝集素的细胞表达有关。总的来说,我们的数据表明,0118 作为糖/碳水化合物结合的变构抑制剂靶向半乳糖凝集素-1。这项工作为抗肿瘤冠醚化合物 0118 的临床开发做出了贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1020/4242090/e3dd511bc4b8/nihms-381819-f0001.jpg

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