| Literature DB >> 29777796 |
Qian Wang1, Shi-Bing Li1, Yi-Ying Zhao2, Da-Nian Dai1, Hui Du1, Yan-Zhu Lin1, Jia-Cong Ye1, Jing Zhao1, Wei Xiao1, Yan Mei1, Yi-Tai Xiao1, Shi-Chu Liu3, Yan Li1, Yun-Fei Xia1, Er-Wei Song4, Gang-Hua Tang5, Wei-Guang Zhang1, Zhi-Jian Li1, Xiao-Bin Zheng1, De-Hai Cao1, Man-Zhi Li1, Qian Zhong1, Zhong-Ping Chen1, Chao-Nan Qian1, Wei Fan6, Guo-Kai Feng7, Mu-Sheng Zeng8.
Abstract
The sodium pump Na+/K+ ATPase a1 subunit(NKA a1), an attractive cancer-related biomarker and therapeutic target, is closely related to the development and progression of several cancers including breast cancer. Currently, a NKA a1 inhibitor, UNBS1450, has already evidenced its great therapeutic potential in personalized cancer treatment. The ability of non-invasive imaging of NKA a1 expression would be useful for selecting cancer patients who may benefit from this drug. Here, we identified an S3 peptide that is specifically homed to breast cancer by phage display. All data of in vitro and in vivo experiments suggested the excellent targeting character of the S3 peptide. As the binding activity of the S3 phage was positively correlated to the level of NKA α1 expression in various breast cancer cells, NKA α1 was validated as the primary target of the S3 peptide. Based on immunohistochemistry staining result of 107 breast cancer patients, NKA α1 was verified to be a novel tracking marker and a prognostic predictor for breast cancer. Importantly, we proposed and validated an S3 peptide-based radiotracer 18F-ALF-NOTA-S3 for PET (Positron Emission Tomography) imaging of breast cancer and other NKA α1-overexpressing cancers, including hepatocellular carcinoma and non-small cell lung cancer, in mouse models. Our findings demonstrated the potential application of 18F-ALF-NOTA-S3 for visualization of NKA α1-positive lesions, which provide a new approach to character tumor phenotypic imaging.Entities:
Keywords: Breast cancer; Na(+)/K(+) ATPase a1; Phage display; Positron emission tomography; Targeting peptide
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Year: 2018 PMID: 29777796 DOI: 10.1016/j.jconrel.2018.05.019
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776