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    Quantitative characterization of duodenal gastrinoma autofluorescence using multiphoton microscopy

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    Quan-MPM-DGAST-Accepted-Manusc ...
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    Author
    Knapp, Thomas G
    Duan, Suzann
    Merchant, Juanita L
    Sawyer, Travis W
    Affiliation
    Department of Biomedical Engineering, University of Arizona
    College of Medicine, University of Arizona
    Wyant College of Optical Sciences, University of Arizona
    Issue Date
    2022-12-14
    Keywords
    GEP-NET
    advanced microscopy
    duodenal gastrinoma
    Multiphoton Microscopy
    neuroendocrine tumor
    optical diagnostics
    quantitative microscopy
    secondharmonic generation
    tissue classification
    two-photon excited fluorescence
    
    Metadata
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    Publisher
    John Wiley and Sons Inc
    Citation
    Knapp, T. G., Duan, S., Merchant, J. L., & Sawyer, T. W. (2022). Quantitative characterization of duodenal gastrinoma autofluorescence using multiphoton microscopy. Lasers in Surgery and Medicine.
    Journal
    Lasers in surgery and medicine
    Rights
    © 2022 Wiley Periodicals LLC.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Background: Duodenal gastrinomas (DGASTs) are neuroendocrine tumors that develop in the submucosa of the duodenum and produce the hormone gastrin. Surgical resection of DGASTs is complicated by the small size of these tumors and the tendency for them to develop diffusely in the duodenum. Endoscopic mucosal resection of DGASTs is an increasingly popular method for treating this disease due to its low complication rate but suffers from poor rates of pathologically negative margins. Multiphoton microscopy can capture high-resolution images of biological tissue with contrast generated from endogenous fluorescence (autofluorescence [AF]) through two-photon excited fluorescence (2PEF). Second harmonic generation is another popular method of generating image contrast with multiphoton microscopy (MPM) and is a light-scattering phenomenon that occurs predominantly from structures such as collagen in biological samples. Some molecules that contribute to AF change in abundance from processes related to the cancer disease process (e.g., metabolic changes, oxidative stress, and angiogenesis). Study Design/Materials and Methods: MPM was used to image 12 separate patient samples of formalin-fixed and paraffin-embedded duodenal gastrinoma slides with a second-harmonic generation (SHG) channel and four 2PEF channels. The excitation and emission profiles of each 2PEF channel were tuned to capture signal dominated by distinct fluorophores with well-characterized fluorescent spectra and known connections to the physiologic changes that arise in cancerous tissue. Results: We found that there was a significant difference in the relative abundance of signal generated in the 2PEF channels for regions of DGASTs in comparison to the neighboring tissues of the duodenum. Data generated from texture feature extraction of the MPM images were used in linear discriminant analysis models to create classifiers for tumor versus all other tissue types before and after principal component analysis (PCA). PCA improved the classifier accuracy and reduced the number of features required to achieve maximum accuracy. The linear discriminant classifier after PCA distinguished between tumor and other tissue types with an accuracy of 90.6%−93.8%. Conclusions: These results suggest that multiphoton microscopy 2PEF and SHG imaging is a promising label-free method for discriminating between DGASTs and normal duodenal tissue which has implications for future applications of in vivo assessment of resection margins with endoscopic MPM.
    Note
    12 month embargo; first published: 14 December 2022
    EISSN
    1096-9101
    PubMed ID
    36515355
    DOI
    10.1002/lsm.23619
    Version
    Final accepted manuscript
    ae974a485f413a2113503eed53cd6c53
    10.1002/lsm.23619
    Scopus Count
    Collections
    UA Faculty Publications

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