| Literature DB >> 24656799 |
Masato Tamura1, Hirofumi Matsui2, Shiho Hirohara3, Kiyomi Kakiuchi4, Masao Tanihara4, Naruto Takahashi5, Kozi Nakai5, Yasukazu Kanai6, Hiroshi Watabe6, Jun Hatazawa7.
Abstract
Positron-emission tomography (PET) can be used to visualize active stage cancer. Fluorine-18 ([(18)F])-labeled 2-([(18)F])2-deoxy-2-fluoroglucose (([(18)F])-FDG), which accumulates in glucose-dependent tissues, is a good cancer-targeting tracer. However, ([(18)F])-FDG is obscured in glucose-dependent normal tissues. In this study, we assessed the cancer-selective accumulation of zinc-labeled glycoconjugated 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin (ZnGlc1-4), both in vitro and in vivo. Experiments using both normal and cancer cells confirmed the relationship between cancer cell-selective accumulation and the substitution numbers and orientations of glycoconjugated porphyrins. ZnGlctrans-2 accumulated at greater levels in cancer cells compared with other glycoconjugated porphyrins. PET imaging showed that ZnGlctrans-2 accumulated in tumor.Entities:
Keywords: Cancer selective accumulation; Positron emission tomography; [(62)Zn]-labeling PET tracer; [(62)Zn]-zinc porphyrins
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Year: 2014 PMID: 24656799 DOI: 10.1016/j.bmc.2014.02.021
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641