| Literature DB >> 33096584 |
Rui Obara1, Mako Kamiya1,2, Yoko Tanaka3, Atsuki Abe1, Ryosuke Kojima1,2, Tokuichi Kawaguchi3,4, Minoru Sugawara4, Akiko Takahashi2,3, Tetsuo Noda3, Yasuteru Urano1,5,6.
Abstract
γ-Glutamyltranspeptidase (GGT) is overexpressed in several types of cancer. Existing GGT-targeting fluorescence probes can image these cancers, but the fluorescent hydrolysis product leaks from the target cancer cells during prolonged incubation or fixation. Here, we present a functionalized fluorescence probe for GGT, 4-CH2 F-HMDiEtR-gGlu, which is designed to generate an azaquinone methide intermediate during activation by GGT; this intermediate reacts with intracellular nucleophiles to generate a fluorescent adduct that is trapped inside the cells, without loss of the target enzyme activity. Application of the probe to patient-derived xenograft (PDX) mice enabled in vivo cancer imaging for a prolonged period and was also compatible with fixation and immunostaining of the cancer tissue.Entities:
Keywords: azaquinone methide; cancer imaging; fluorescence probe; γ-glutamyltranspeptidase
Year: 2020 PMID: 33096584 DOI: 10.1002/anie.202013265
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336