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一种基于多模态纳米粒子的癌症成像探针,同时靶向核仁素、整合素 αvβ3 和 tenascin-C 蛋白。

A multimodal nanoparticle-based cancer imaging probe simultaneously targeting nucleolin, integrin αvβ3 and tenascin-C proteins.

机构信息

Laboratory of Molecular Imaging, Department of Applied Bioscience, CHA Stem Cell Institute, CHA University, 605-21 Yoeksam 1-dong, Gangnam-gu, Seoul 135-081, Republic of Korea.

出版信息

Biomaterials. 2011 Feb;32(4):1130-8. doi: 10.1016/j.biomaterials.2010.10.034. Epub 2010 Nov 10.

Abstract

Molecular imaging of cancers has been characterized based on the sensitivity and selectivity of a single cancer probe targeting a cancer biomarker of a specific cancer cell line. Here, we designed a multimodal nanoparticle-based Simultaneously Multiple Aptamers and RGD Targeting (SMART) cancer probe targeting multiple cancer biomarkers to enhance the specificity and signal sensitivity for various cancers. Transmission electron microscopy revealed that the multimodal SMART cancer probe was spheric and well dispersed. Fluorescence, radioisotope, and magnetic resonance analysis demonstrated that the SMART cancer probe simultaneously targeting the nucleolin, integrin α(v)β(3) and Tnc proteins had dramatically enhanced specificity and signal intensity when used to target cancers from C6, NPA, DU145, HeLa and A549 cells when compared with single cancer probes conjugated with AS1411, RGD or TTA1 targeting a single cancer biomarker. The results demonstrated that the SMART cancer probe will be useful for the diagnosis of different cancers as a cancer master probe.

摘要

基于针对特定癌细胞系的癌症标志物的单一癌症探针的灵敏度和选择性,对癌症的分子成像进行了描述。在这里,我们设计了一种基于多模态纳米粒子的同时靶向多个癌症标志物的多适体和 RGD(SMART)癌症探针,以增强针对各种癌症的特异性和信号灵敏度。透射电子显微镜显示,多模态 SMART 癌症探针呈球形且分散良好。荧光、放射性同位素和磁共振分析表明,当用于靶向 C6、NPA、DU145、HeLa 和 A549 细胞的癌症时,同时靶向核仁素、整合素 α(v)β(3)和 Tnc 蛋白的 SMART 癌症探针与靶向单一癌症标志物的 AS1411、RGD 或 TTA1 连接的单一癌症探针相比,特异性和信号强度显著增强。结果表明,SMART 癌症探针将作为一种癌症主探针,可用于不同癌症的诊断。

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