Low-level whole-brain radiation enhances theranostic potential of single-domain antibody fragments for human epidermal growth factor receptor type 2 (HER2)-positive brain metastases.
dc.contributor.author | Procissi, Daniele | |
dc.contributor.author | Jannetti, Stephen A | |
dc.contributor.author | Zannikou, Markella | |
dc.contributor.author | Zhou, Zhengyuan | |
dc.contributor.author | McDougald, Darryl | |
dc.contributor.author | Kanojia, Deepak | |
dc.contributor.author | Zhang, Hui | |
dc.contributor.author | Burdett, Kirsten | |
dc.contributor.author | Vaidyanathan, Ganesan | |
dc.contributor.author | Zalutsky, Michael R | |
dc.contributor.author | Balyasnikova, Irina V | |
dc.date.accessioned | 2022-10-01T15:27:56Z | |
dc.date.available | 2022-10-01T15:27:56Z | |
dc.date.issued | 2022-01 | |
dc.date.updated | 2022-10-01T15:27:41Z | |
dc.description.abstract | BackgroundSingle-domain antibody fragments (aka VHH, ~ 13 kDa) are promising delivery systems for brain tumor theranostics; however, achieving efficient delivery of VHH to intracranial lesions remains challenging due to the tumor-brain barrier. Here, we evaluate low-dose whole-brain irradiation as a strategy to increase the delivery of an anti- human epidermal growth factor receptor type 2 (HER2) VHH to breast cancer-derived intracranial tumors in mice.MethodsMice with intracranial HER2-positive BT474BrM3 tumors received 10-Gy fractionated cranial irradiation and were evaluated by noninvasive imaging. Anti-HER2 VHH 5F7 was labeled with 18F, administered intravenously to irradiated mice and controls, and PET/CT imaging was conducted periodically after irradiation. Tumor uptake of 18F-labeled 5F7 in irradiated and control mice was compared by PET/CT image analysis and correlated with tumor volumes. In addition, longitudinal dynamic contrast-enhanced MRI (DCE-MRI) was conducted to visualize and quantify the potential effects of radiation on tumor perfusion and permeability.ResultsIncreased 18F-labeled 5F7 intracranial tumor uptake was observed with PET in mice receiving cranial irradiation, with maximum tumor accumulation seen approximately 12 days post initial radiation treatment. No radiation-induced changes in HER2 expression were detected by Western blot, flow cytometry, or on tissue sections. DCE-MRI imaging demonstrated transiently increased tumor perfusion and permeability after irradiation, consistent with the higher tumor uptake of 18F-labeled anti-HER2 5F7 in irradiated mice.ConclusionLow-level brain irradiation induces dynamic changes in tumor vasculature that increase the intracranial tumor delivery of an anti-HER2 VHH, which could facilitate the use of radiolabeled VHH to detect, monitor, and treat HER2-expressing brain metastases. | |
dc.identifier | vdac135 | |
dc.identifier.issn | 2632-2498 | |
dc.identifier.issn | 2632-2498 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Oxford University Press (OUP) | |
dc.relation.ispartof | Neuro-oncology advances | |
dc.relation.isversionof | 10.1093/noajnl/vdac135 | |
dc.subject | HER2 | |
dc.subject | PET | |
dc.subject | VHH | |
dc.subject | breast cancer brain metastases | |
dc.subject | single-domain antibody fragment | |
dc.title | Low-level whole-brain radiation enhances theranostic potential of single-domain antibody fragments for human epidermal growth factor receptor type 2 (HER2)-positive brain metastases. | |
dc.type | Journal article | |
duke.contributor.orcid | Vaidyanathan, Ganesan|0000-0003-3041-8275 | |
duke.contributor.orcid | Zalutsky, Michael R|0000-0002-5456-0324 | |
pubs.begin-page | vdac135 | |
pubs.issue | 1 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Pathology | |
pubs.organisational-group | Radiation Oncology | |
pubs.organisational-group | Radiology | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.publication-status | Published | |
pubs.volume | 4 |
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