Nanoparticles Targeted to Fibroblast Activation Protein Outperform PSMA for MRI Delineation of Primary Prostate Tumors.

fibroblast activation proteins iron oxide nanoparticles magnetic resonance imaging prostate cancer prostate-specific membrane antigen

Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
05 2023
Historique:
revised: 23 01 2023
received: 12 08 2022
medline: 25 5 2023
pubmed: 26 2 2023
entrez: 25 2 2023
Statut: ppublish

Résumé

Accurate delineation of gross tumor volumes remains a barrier to radiotherapy dose escalation and boost dosing in the treatment of solid tumors, such as prostate cancer. Magnetic resonance imaging (MRI) of tumor targets has the power to enable focal dose boosting, particularly when combined with technological advances such as MRI-linear accelerator. Fibroblast activation protein (FAP) is overexpressed in stromal components of >90% of epithelial carcinomas. Herein, the authors compare targeted MRI of prostate specific membrane antigen (PSMA) with FAP in the delineation of orthotopic prostate tumors. Control, FAP, and PSMA-targeting iron oxide nanoparticles were prepared with modification of a lymphotropic MRI agent (FerroTrace, Ferronova). Mice with orthotopic LNCaP tumors underwent MRI 24 h after intravenous injection of nanoparticles. FAP and PSMA nanoparticles produced contrast enhancement on MRI when compared to control nanoparticles. FAP-targeted MRI increased the proportion of tumor contrast-enhancing black pixels by 13%, compared to PSMA. Analysis of changes in R2 values between healthy prostates and LNCaP tumors indicated an increase in contrast-enhancing pixels in the tumor border of 15% when targeting FAP, compared to PSMA. This study demonstrates the preclinical feasibility of PSMA and FAP-targeted MRI which can enable targeted image-guided focal therapy of localized prostate cancer.

Identifiants

pubmed: 36840671
doi: 10.1002/smll.202204956
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2204956

Informations de copyright

© 2023 The Authors. Small published by Wiley-VCH GmbH.

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Auteurs

Nicole Dmochowska (N)

Future Industries Institute, University of South Australia, Adelaide, South Australia, 5095, Australia.

Valentina Milanova (V)

Future Industries Institute, University of South Australia, Adelaide, South Australia, 5095, Australia.

Ramesh Mukkamala (R)

Department of Chemistry and Institute for Drug Discovery, Purdue University, West Lafayette, IN, 47907, USA.

Kwok Keung Chow (KK)

Future Industries Institute, University of South Australia, Adelaide, South Australia, 5095, Australia.

Nguyen T H Pham (NTH)

Key Centre for Polymers and Colloids, School of Chemistry, The University of Sydney, Sydney, New South Wales, 2006, Australia.

Madduri Srinivasarao (M)

Department of Chemistry and Institute for Drug Discovery, Purdue University, West Lafayette, IN, 47907, USA.

Lisa M Ebert (LM)

Centre for Cancer Biology, University of South Australia; SA Pathology; Cancer Clinical Trials Unit, Royal Adelaide Hospital; Adelaide Medical School, University of Adelaide, Adelaide, South Australia, 5000, Australia.

Timothy Stait-Gardner (T)

Nanoscale Organisation and Dynamics Group, Western Sydney University, Sydney, New South Wales, 2560, Australia.

Hien Le (H)

Department of Radiation Oncology, Royal Adelaide Hospital, Adelaide, South Australia, 5000, Australia.

Anil Shetty (A)

Ferronova Pty Ltd, Mawson Lakes, South Australia, 5095, Australia.

Melanie Nelson (M)

Ferronova Pty Ltd, Mawson Lakes, South Australia, 5095, Australia.

Philip S Low (PS)

Department of Chemistry and Institute for Drug Discovery, Purdue University, West Lafayette, IN, 47907, USA.

Benjamin Thierry (B)

Future Industries Institute, University of South Australia, Adelaide, South Australia, 5095, Australia.

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