Synthesis and Preclinical Evaluation of [68Ga]SP94 for Micro-PET Imaging of GRP78 Expression in Hepatocellular Carcinoma

被引:5
|
作者
Xu, Yifei [1 ]
Jiang, Jinhui [2 ]
Wang, Hui [2 ]
Yu, Wenjing [2 ]
Sun, Guoping [1 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Oncol, Hefei 230022, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Nucl Med, Hefei 230022, Peoples R China
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2021年 / 12卷 / 10期
基金
中国国家自然科学基金;
关键词
GRP78; micro-PET imaging; Ga-68]SP94; molecular probe; hepatocellular carcinoma; CANCER; PROTEINS;
D O I
10.1021/acsmedchemlett.1c00350
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glucose-regulated protein 78 (GRP78) is overexpressed in a wide variety of solid tumors, serving as a well-characterized target for tumor imaging or therapy. In this work, we developed a GRP78-responsive radiotracer (DOTA(68)Ga)-Gly-Gly-Gly-Ser-Phe-Ser-Ile-Ile-His-Thr-Pro-Ile-Leu-Pro-Leu-Gly-Gly-Cys ([Ga-68]SP94) for hepatocellular carcinoma (HCC) micro-PET imaging. DOTA-SP94 was synthesized by solid phase synthesis and then radiolabeled with (GaCl3)-Ga-68 with >99% radiochemical purity. The expression levels of GRP78 in HepG(2) cells were confirmed by Western blotting. In vitro and in vivo study of [(68) Ga]SP94 showed high stability and high uptake in GRP78-overexpressing HepG(2) cells and tumor, fast clearance, and low nontarget uptake. Micro-PET images showed excellent tumor accumulation of [Ga-68]SP94 in the HepG(2)-implanted nude mice tumor model. Additionally, the radiotracer uptake in HepG(2) tumors can be blocked by unlabeled DOTA-SP94, suggesting that the tracer uptake by HCC was receptor-mediated. We envision that our radiotracer can be used for noninvasive imaging of HCC and is worthy of further clinical investigations.
引用
收藏
页码:1553 / 1558
页数:6
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