Design and Synthesis of Novel Near-Infrared Fluorescence Probes Based on an Open Conformation of a Cytochrome P450 1B1 Complex for Molecular Imaging of Colorectal Tumors.
Dongmei ChenRuining LiQi ShaoZhihao WuJiahua CuiQingqing MengShaoshun LiPublished in: Journal of medicinal chemistry (2023)
Cytochrome P450 1B1 (CYP1B1) is induced during the early stage of cancer and is universally overexpressed in tumors. Thus, it was considered as a potential biomarker for the monitoring of cancer. In this study, we designed and synthesized CYP1B1-targeted near-infrared (NIR) fluorescence molecular probes based on the latest reported open conformation of the CYP1B1-α-naphthoflavone (ANF) complex. According to the architecture of the open channel, we introduced linkers and a Cy5.5 fragment at the 5' position of ANF derivatives with strong CYP1B1 inhibitory activity to obtain probes 19 - 21 . Then, in vitro cell-based studies showed that the probes could be enriched in tumor cells by binding to CYP1B1. During in vivo and ex vivo imaging in a xenograft mouse model, probe 19 with the best binding affinity was proven to be able to identify tumor sites in both fluorescence imaging and photoacoustic imaging modes.
Keyphrases
- fluorescence imaging
- photodynamic therapy
- early stage
- single molecule
- papillary thyroid
- mouse model
- living cells
- minimally invasive
- high resolution
- small molecule
- squamous cell
- single cell
- fluorescent probe
- mesenchymal stem cells
- bone marrow
- lymph node
- binding protein
- stem cells
- diabetic rats
- energy transfer
- sentinel lymph node
- capillary electrophoresis