乳腺癌
肽
癌症研究
体内
菁
PALB2
医学
噬菌体展示
癌症
肿瘤科
内科学
化学
生物
荧光
生物技术
生物化学
物理
量子力学
突变
种系突变
基因
作者
Mengdie Chen,Anying Zhu,Furong Zhu,Ziwen Lei,Tao Huang,Shengnan Du,Dongdong Wang,Xiaoyu Zhang,Huan Min,Yingqiu Qi,Guangjun Nie
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-11-17
卷期号:17 (10): 9044-9051
被引量:7
标识
DOI:10.1007/s12274-023-6268-8
摘要
Breast cancer remains a leading cause of morbidity and mortality among women worldwide, emphasizing the urgent need for enhanced diagnostic and therapeutic approaches. Leucine-rich-alpha-2-glycoprotein 1 (LRG1) has emerged as a notable target due to its markedly elevated expression in breast tumors, suggesting the viability of LRG1 as a theranostic target. In our study, we employed phage display technology to identify a peptide, termed ET, that binds to LRG1 with a dissociation constant of 48.4 µM. After modified with fluorescent cyanine dye, the ET peptide showcased effective tumor-targeting imaging across three different primary breast tumor models and a metastatic breast tumor model. We also undertook a comprehensive safety evaluation, which verified the good biosafety credentials of ET peptide. In summary, the ET peptide identified in this study shows effective LRG1-targeting ability both in vitro and in vivo, thus exhibiting immense potential for clinical translation.
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