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VCAM-1-targeted magnetic resonance imaging improves detection of the tumor-brain interface

Cheng, Vinton W. T.; de Pennington, Nicholas; Zakaria, Rasheed; Larkin, James R.; Serres, Sébastien; Sarkar, Manjima; Kirkman, Matthew A.; Bristow, Claire; Croal, Paula; Plaha, Puneet; Campo, Leticia; Chappell, Michael A.; Lord, Simon; Jenkinson, Michael D.; Middleton, Mark R.; Sibson, Nicola R.

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Authors

Vinton W. T. Cheng

Nicholas de Pennington

Rasheed Zakaria

James R. Larkin

Dr SEBASTIEN SERRES Sebastien.Serres@nottingham.ac.uk
ASSISTANT PROFESSOR IN METABOLIC BIOCHEMISTRY

Manjima Sarkar

Matthew A. Kirkman

Claire Bristow

Paula Croal

Puneet Plaha

Leticia Campo

Michael A. Chappell

Simon Lord

Michael D. Jenkinson

Mark R. Middleton

Nicola R. Sibson



Abstract

Purpose:
Despite optimal local therapy, tumor cell invasion into normal brain parenchyma frequently results in recurrence in patients with solid tumors. The aim of this study was to determine whether microvascular inflammation can be targeted to better delineate the tumor-brain interface through vascular cell adhesion molecule-1 (VCAM-1)-targeted MRI.

Experimental Design:
Intracerebral xenograft rat models of MDA231Br-GFP (breast cancer) brain metastasis and U87MG (glioblastoma) were used to histologically examine the tumor-brain interface and to test the efficacy of VCAM-1–targeted MRI in detecting this region. Human biopsy samples of the brain metastasis and glioblastoma margins were examined for endothelial VCAM-1 expression.

Results:
The interface between tumor and surrounding normal brain tissue exhibited elevated endothelial VCAM-1 expression and increased microvessel density. Tumor proliferation and stemness markers were also significantly upregulated at the tumor rim in the brain metastasis model. T2*-weighted MRI, following intravenous administration of VCAM-MPIO, highlighted the tumor-brain interface of both tumor models more extensively than gadolinium-DTPA–enhanced T1-weighted MRI. Sites of VCAM-MPIO binding, evident as hypointense signals on MR images, correlated spatially with endothelial VCAM-1 upregulation and bound VCAM-MPIO beads detected histologically. These findings were further validated in an orthotopic medulloblastoma model. Finally, the tumor-brain interface in human brain metastasis and glioblastoma samples was similarly characterized by microvascular inflammation, extending beyond the region detectable using conventional MRI.

Conclusions:
This work illustrates the potential of VCAM-1–targeted MRI for improved delineation of the tumor-brain interface in both primary and secondary brain tumors.

Citation

Cheng, V. W. T., de Pennington, N., Zakaria, R., Larkin, J. R., Serres, S., Sarkar, M., Kirkman, M. A., Bristow, C., Croal, P., Plaha, P., Campo, L., Chappell, M. A., Lord, S., Jenkinson, M. D., Middleton, M. R., & Sibson, N. R. (2022). VCAM-1-targeted magnetic resonance imaging improves detection of the tumor-brain interface. Clinical Cancer Research, 28(11), 2385-2396. https://doi.org/10.1158/1078-0432.ccr-21-4011

Journal Article Type Article
Acceptance Date Mar 17, 2022
Online Publication Date Mar 21, 2022
Publication Date Jun 1, 2022
Deposit Date Jun 20, 2025
Publicly Available Date Jun 23, 2025
Journal Clinical Cancer Research
Print ISSN 1078-0432
Electronic ISSN 1557-3265
Publisher American Association for Cancer Research
Peer Reviewed Peer Reviewed
Volume 28
Issue 11
Pages 2385-2396
DOI https://doi.org/10.1158/1078-0432.ccr-21-4011
Keywords Cancer Research; Oncology
Public URL https://nottingham-repository.worktribe.com/output/7766956
Publisher URL https://aacrjournals.org/clincancerres/article/28/11/2385/698936/VCAM-1-targeted-MRI-Improves-Detection-of-the

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