4.7 Article

Novel fluorescent GLUT1 inhibitor for precision detection and fluorescence image-guided surgery in oral squamous cell carcinoma

Journal

INTERNATIONAL JOURNAL OF CANCER
Volume 151, Issue 3, Pages 450-462

Publisher

WILEY
DOI: 10.1002/ijc.34049

Keywords

fluorescence molecular imaging; glucose transporter type 1; image-guided surgery; mouth neoplasms; WZB117

Categories

Funding

  1. Beijing Natural Science Foundation [7212207]
  2. Ministry of Science and Technology of China [2017YFA0205200, 2017YFA0700401]
  3. China National Key Research and Development Plan Project [2017YFB1304300]
  4. National Natural Science Foundation of China [62027901, 81227901, 81470083, 81527805, 81871514]
  5. Subsidiary of PLA Major Project [AWS17J004]

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A novel fluorescent imaging probe, WZB117-IR820, was synthesized for early detection and fluorescence image-guided surgery in oral squamous cell carcinoma (OSCC), with potential clinical applications.
Early detection and complete resection of oral squamous cell carcinoma (OSCC) are crucial to improving patient survival and prognosis. However, specifically targeted imaging probes for OSCC detection are limited. Our study aimed to synthesize a novel near-infrared fluorescence (NIRF) probe for precision detection and fluorescence image-guided surgery in OSCC. Bioinformatics data indicated that glucose transporter 1 (GLUT1) is highly expressed in patients with OSCC. We demonstrated high and specific GLUT1 expression upon immunohistochemical staining of samples from 20 patients with OSCC. The specific expression of GLUT1 was further validated in both human OSCC cell lines and OSCC tumor xenografts. Based on these findings, the GLUT1 inhibitor WZB117 was utilized to synthesize a novel NIRF imaging probe, WZB117-IR820. The fluorescence molecular imaging data revealed that WZB117-IR820 could specifically bind to the tumor areas in an orthotopic OSCC mouse model after intravenous injection and could be further applied for precision fluorescence image-guided surgery with no residual tumor in the orthotopic CAL27-fLUC mouse tumor model. For further clinical translational application in patients with OSCC, precise delineation of OSCC tumor areas was achieved after topical application of the WZB117-IR820 imaging probe and was validated by histopathological and immunohistochemical analyses. In conclusion, we synthesized a novel fluorescent imaging probe, WZB117-IR820, which has potential clinical applications for early detection and fluorescence image-guided surgery in OSCC with no observable toxicity.

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