Abstract
Evaluation of Gastrointestinal Stromal Tumors (GIST) during initial clinical staging, surgical intervention, and postoperative management can be challenging. Current imaging modalities (e.g., PET and CT scans) lack sensitivity and specificity. Therefore, advanced clinical imaging modalities that can provide clinically relevant images with high resolution would improve diagnosis. KIT is a tyrosine kinase receptor overexpressed on GIST. Here, the application of a specific DNA aptamer targeting KIT, decorated onto a fluorescently labeled porous silicon nanoparticle (pSiNP), is used for the in vitro & in vivo imaging of GIST. This nanoparticle platform provides high-fidelity GIST imaging with minimal cellular toxicity. An in vitro analysis shows greater than 15-fold specific KIT protein targeting compared to the free KIT aptamer, while in vivo analyses of GIST-burdened mice that had been injected intravenously (IV) with aptamer-conjugated pSiNPs show extensive nanoparticle-to-tumor signal co-localization (>90% co-localization) compared to control particles. This provides an effective platform for which aptamer-conjugated pSiNP constructs can be used for the imaging of KIT-expressing cancers or for the targeted delivery of therapeutics.
| Original language | English |
|---|---|
| Pages (from-to) | 17700-17713 |
| Number of pages | 14 |
| Journal | Nanoscale |
| Volume | 14 |
| Issue number | 47 |
| DOIs | |
| State | Published - Nov 16 2022 |
Bibliographical note
Publisher Copyright:© 2022 The Royal Society of Chemistry.
Funding
The authors acknowledge the use of facilities and instrumentation supported by the National Science Foundation through the UC San Diego Materials Research Science and Engineering Center (UCSD MRSEC) DMR-2011924 and by the San Diego Nanotechnology Infrastructure (SDNI) of UCSD, a member of the National Nanotechnology Coordinated Infrastructure, which is supported by the National Science Foundation Grant ECCS-1542148. The authors also would like to thank the University of California, San Diego – Cellular and Molecular Medicine Electron Microscopy Core (UCSD-CMM-EM Core, RRID: SCR_022039) for equipment access and technical assistance. The UCSD-CMM-EM Core is partially supported by the National Institutes of Health Award number S10OD023527. The authors thank UCSD's Altman Clinical and Translational Research Institute (ACTRI) for the 2020 Pilot Project Grant (P.R.), National Institutes of Health Grant UL1TR001442. In addition, S.V. acknowledges support from UCSD's Chancellor's Interdisciplinary Collaboratories as well as the Natural Sciences and Engineering Research Council of Canada Postgraduate Scholarship – Doctoral program (NSERC PGS-D). The authors acknowledge the use of facilities and instrumentation supported by the National Science Foundation through the UC San Diego Materials Research Science and Engineering Center (UCSD MRSEC) DMR-2011924 and by the San Diego Nanotechnology Infrastructure (SDNI) of UCSD, a member of the National Nanotechnology Coordinated Infrastructure, which is supported by the National Science Foundation Grant ECCS-1542148. The authors also would like to thank the University of California, San Diego - Cellular and Molecular Medicine Electron Microscopy Core (UCSD-CMM-EM Core, RRID: SCR_022039) for equipment access and technical assistance. The UCSD-CMM-EM Core is partially supported by the National Institutes of Health Award number S10OD023527. The authors thank UCSD's Altman Clinical and Translational Research Institute (ACTRI) for the 2020 Pilot Project Grant (P.R.), National Institutes of Health Grant UL1TR001442. In addition, S.V. acknowledges support from UCSD's Chancellor's Interdisciplinary Collaboratories as well as the Natural Sciences and Engineering Research Council of Canada Postgraduate Scholarship - Doctoral program (NSERC PGS-D).
| Funders | Funder number |
|---|---|
| ACTRI | UL1TR001442 |
| UCSD's Altman Clinical and Translational Research Institute | |
| National Science Foundation Arctic Social Science Program | |
| National Institutes of Health (NIH) | S10OD023527 |
| National Childhood Cancer Registry – National Cancer Institute | R01CA226803 |
| University of California San Diego Health | SCR_022039 |
| Materials Research Science and Engineering Center, University of California, San Diego | ECCS-1542148, DMR-2011924 |
| Natural Sciences and Engineering Research Council of Canada |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
ASJC Scopus subject areas
- General Materials Science
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