Tumor Imaging Using Radiolabeled Matrix Metalloproteinase-Activated Anthrax Proteins.


Journal

Journal of nuclear medicine : official publication, Society of Nuclear Medicine
ISSN: 1535-5667
Titre abrégé: J Nucl Med
Pays: United States
ID NLM: 0217410

Informations de publication

Date de publication:
10 2019
Historique:
received: 22 01 2019
accepted: 13 03 2019
pubmed: 8 4 2019
medline: 14 4 2020
entrez: 8 4 2019
Statut: ppublish

Résumé

Increased activity of matrix metalloproteinases (MMPs) is associated with worse prognosis in different cancer types. The wild-type protective antigen (PA-WT) of the binary anthrax lethal toxin was modified to form a pore in cell membranes only when cleaved by MMPs (to form PA-L1). Anthrax lethal factor (LF) is then able to translocate through these pores. Here, we used a

Identifiants

pubmed: 30954944
pii: jnumed.119.226423
doi: 10.2967/jnumed.119.226423
pmc: PMC6785798
doi:

Substances chimiques

Antigens, Bacterial 0
Bacterial Toxins 0
Indium Radioisotopes 0
anthrax toxin 0
Matrix Metalloproteinases EC 3.4.24.-
MMP2 protein, human EC 3.4.24.24
Matrix Metalloproteinase 2 EC 3.4.24.24
MMP14 protein, human EC 3.4.24.80
Matrix Metalloproteinase 14 EC 3.4.24.80

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1474-1482

Subventions

Organisme : Medical Research Council
ID : MR/P018661/1
Pays : United Kingdom

Informations de copyright

© 2019 by the Society of Nuclear Medicine and Molecular Imaging.

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Auteurs

Mary-Ann Elvina Xavier (MA)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Shihui Liu (S)

Proteases and Tissue Remodeling Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.
Microbial Pathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland; and.

Thomas H Bugge (TH)

Proteases and Tissue Remodeling Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.

Julia Baguña Torres (JB)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Michael Mosley (M)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Samantha L Hopkins (SL)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Phillip D Allen (PD)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Georgina Berridge (G)

Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Iolanda Vendrell (I)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.
Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Roman Fischer (R)

Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Veerle Kersemans (V)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Sean Smart (S)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom.

Stephen H Leppla (SH)

Microbial Pathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland; and.

Bart Cornelissen (B)

Department of Oncology, CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, United Kingdom bart.cornelissen@oncology.ox.ac.uk.

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Classifications MeSH