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设计、合成及细胞色素 P450 1B1 靶向的用于结直肠肿瘤检测的分子成像探针的生物学评价。

Design, Synthesis, and Biological Evaluation of Cytochrome P450 1B1 Targeted Molecular Imaging Probes for Colorectal Tumor Detection.

机构信息

School of Pharmacy , Shanghai Jiao Tong University , 800 Dongchuan Road , Shanghai 200240 , China.

出版信息

J Med Chem. 2018 Dec 13;61(23):10901-10909. doi: 10.1021/acs.jmedchem.8b01633. Epub 2018 Nov 27.

Abstract

Cytochrome P450 1B1 (CYP1B1) was found to be universally expressed in various tumors. Herein, we reported near-infrared fluorescent imaging probes for tumor detection via visualizing CYP1B1. After introducing the linker to a CYP1B1 selective inhibitor we found previously, we got the resulting compound 5b which kept strong inhibition ability against CYP1B1 (IC = 8.7 ± 1.2 nM) and high selectivity. Then, in vitro microscope studies and cell binding assay of probes indicated that the corresponding probe 6b could specifically be accumulated in CYP1B1 overexpressed colorectal cancer cell HCT-15 and showed satisfying binding affinity to target. During the in vivo noninvasive optical imaging, 6b was proved to rapidly lighten tumor in vivo as early as 6 h after injection. This work is the first attempt to visualize CYP1B1 for noninvasive imaging of tumor which could provide new approach for tumor diagnosis.

摘要

细胞色素 P450 1B1(CYP1B1)被发现普遍存在于各种肿瘤中。在此,我们报告了通过可视化 CYP1B1 进行肿瘤检测的近红外荧光成像探针。在引入我们之前发现的 CYP1B1 选择性抑制剂的连接子后,得到了具有强 CYP1B1 抑制能力(IC = 8.7 ± 1.2 nM)和高选择性的化合物 5b。然后,探针的体外显微镜研究和细胞结合实验表明,相应的探针 6b 可以特异性地在 CYP1B1 过表达的结直肠癌细胞 HCT-15 中积累,并表现出对靶标的满意结合亲和力。在体内非侵入性光学成像期间,6b 在注射后 6 小时内即可迅速减轻肿瘤,这是首次尝试可视化 CYP1B1 进行肿瘤的非侵入性成像,为肿瘤诊断提供了新的方法。

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