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Discrimination and Characterization of Heterocellular Populations Using Quantitative Imaging Techniques
Published on: June 30, 2017
Multi-modality imaging to determine the cellular heterogeneity of nasopharyngeal carcinoma components
Weidong Zhang1, Yanling Zhang, Shi Ke
1State Key Laboratory of Oncology in South China, Department of Imaging and Interventional Radiology, Cancer Center, Sun Yat-sen University, Guangzhou, Guangdong, 510060, P. R. China.
Abstract:
Nasopharyngeal carcinoma (NPC) is an endemic public health problem in South and Southeast Asian countries. The disease components at the molecular level are unclear and need exploration for the development of future individualized molecular medicine. The purpose of this study was to test the feasibility of target-specific agents to detect different components of NPC. The binding capability of human NPC cell lines was determined by incubation with either agents that specifically target the metabolic status, host cytokines, and stroma. Mice bearing human NPC xenografts were injected with the same test agents plus a clinical molecular imaging agent (18F-fluorodeoxyglucose) and computer tomography (CT) contrast agent. In vitro cell studies have demonstrated that target-specific agents bind to NPC cells with significantly higher signal intensities. Those agents not only bound to the cell membrane but also penetrated into the cytosol and cell nuclei. In vivo imaging demonstrated that the human NPC xenografts revealed high glucose uptake and a profound vasculature in the tumor. All agents were bound to the tumor regions with a high tumor-to-muscle ratio. Finally, all imaging data were validated by histopathological results. Multiple, target-specific agents determine the dynamic and heterogeneous components of NPC at the molecular level.
Insights
Target-specific agents effectively detect molecular components of nasopharyngeal carcinoma (NPC). This study shows these agents bind NPC cells and tumors, aiding future molecular medicine development for this endemic cancer.
Area of Science:
- Oncology
- Molecular Imaging
- Biotechnology
Background:
- Nasopharyngeal carcinoma (NPC) is a significant public health issue in South and Southeast Asia.
- Understanding NPC's molecular components is crucial for developing personalized molecular medicine.
- Current knowledge of NPC's molecular landscape requires further exploration.
Purpose of the Study:
- To evaluate the feasibility of using target-specific agents for detecting diverse NPC components.
- To assess the binding capabilities of agents targeting metabolic status, cytokines, and stroma in NPC.
- To validate imaging findings with histopathological analysis.
Main Methods:
- In vitro incubation of human NPC cell lines with target-specific agents.
- In vivo imaging of human NPC xenografts in mice using test agents and clinical imaging modalities (18F-FDG, CT contrast).
- Histopathological validation of imaging data.
Main Results:
- Target-specific agents exhibited significantly higher signal intensities when binding to NPC cells.
- Agents demonstrated binding to cell membranes, cytosol, and nuclei.
- In vivo imaging revealed high tumor glucose uptake, prominent vasculature, and high tumor-to-muscle ratios for all agents.
- Histopathology confirmed imaging findings.
Conclusions:
- Multiple target-specific agents can effectively delineate the dynamic and heterogeneous molecular characteristics of nasopharyngeal carcinoma.
- This approach holds promise for advancing individualized molecular medicine for NPC.
- The study validates the utility of targeted agents in characterizing NPC at a molecular level.
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