Metadata

Dataset ID: 8
Back to List

Study Design
Study Design Background Synthesis and labelling with F-18 of (2S,4R)-4-fluoroglutamine (4-FGln). In vitro evaluation using two cancers cell line and in vivo imaging in a multiple myeloma mouse model, in comparison to 18F-FDG. Evaluation of Bortezomib treatment efficacy.
Study Description Chemical synthesis and characterization of 4-FGln. In vitro and in vivo evaluation by PET-CT of the new radiotracer [18F]4-FGln in the multiple myeloma detection and treatment. Comparison to [18F]FDG
Study Type preclinical
Study Subtype in vivo and ex-vivo
Publication
Paper Linked yes
Paper Title [18F](2S,4R)-4-Fluoroglutamine as a New Positron Emission Tomography Tracer in Myeloma
Paper Authors Valtorta S, Toscani D, Chiu M,…Moresco RM, … and Giuliani N
Affiliation University of Milano - Bicocca, University of Parma, IRCCS San Raffale of Milan, IBFM-CNR, Italy
Paper Journal Frontiers in Oncology
Paper Year 2021
Paper Doi https://doi.org/10.3389/fonc.2021.760732
Open Access yes
Updated Year 2022
Study Component
Multi Modality Images not
Imaging Modality PET
Radiation yes
Imaging Coverage PET: whole body
Imaging Target Glutamine and glucose metabolism
Dataset Information
Institution IBFM-CNR
Pi Moresco Rosa Maria
Co Pi Valtorta Silvia
Country Of Institution Italy
Imaging Facility Laboratory of molecular imaging for small animal
Euro Bio Imaging Node MMMI
Country Of Imaging Facility Italy
In Vivo Experimental Parameters
Number Of Groups 2 tumor models: asyngeneic model (murine Vk12598 cells) and a xenograft model (JJN3 cells). JJN3 used also for treatment response.
Types Of Groups 1. syngeneic model (murine Vk12598 cells) for tracer biodistribution 2. xenograft model (JJN3 cells) for kinetic and biodistribution 3. JJN3 xenograft model control group (treated with vehicle) 4. JJN3 xenograft model control group (treated with Bortezomib)
Overall Sample Size 27
Disease Model multiple myeloma
Organ Or Tissue total body
Sample Size For Each Group group 1: 5; group 2: 7; group 3: 8; group 4: 7.
Power Calculation G*power
Randomization mice were randomly assigned to control or treated group
Blinding no
Outcome Measures Relative tumor growth, weight loss, general well being of the mice
Statistical Methods Unpaired t test and Wilcoxon matched-pairs signed rank-test and Unpaired Mann-Whitney test.
Species Mice
Strain C57BL/6J, NOD.SCID
Immune Status Immunecompetent and immunodeficient
Sex Female
Age Older than 6 weeks
Age At Start Experiment Older than 6 weeks
Age At Scanning Experiment S Older than 6 weeks
Weight About 25 g
Weight At Start Experiment About 25 g
Weight At End Experiment About 25 g
Source Of Animals Charles river Laboratories
Registry Number Of Animal Authorization 34/2018-PR
Experimental Procedures
Pharmacological Drug Bortezomib
Company n.a.
Formulation Solution
Drug Dose 1
Volume 0,03
Concentration 1 mg/ml
Site Route Of Administration intravenous
Frequency Of Administration two times (d0 and d4)
Vehicle Or Carrier Solution Formulation Saline
Drug Batch Sample Number n.a.
Blood Sampling yes
Blood Sampling Method retroorbital bleeding
Blood Sample Volume 50 ul
Blood Timing one a week for 3 weeks in the syngeneic model
Surgical Procedures Including Sham Surgery no
Pathogen Infection Intervention And Control no
Analgesic Plan To Relieve Pain Suffering And Distress no
Anesthesia Type Gas
Duration 30
Anesthesia Drugs Isofluran
Anesthesia Dose 2% in 1L per minute/air mix
Monitoring Regime software remote control of the animal's vital functions (temperature, heartbeat and breathing)
Euthanasia yes
Method CO2 plus cervical dislocation
Histology no
Frequency Of Imaging 2-3 time point for both radioligands
Timing Of Imaging cell line Vk12598: three time points (1 per week after cells injection); cell line JJN3: two time points (one and two weeks and before and after treatment)
Overall Scan Length 90 min for PET-CT kinetic of [18F]4-FGln; 30 minutes for PET-CT biodistribution and therapy response
Contrast Agent Or Radio Isotope Or Challenge With Gas Molecule Yes
Contrast Agent Commercial Drug [18F]4-FGln; [18F]FDG
Contrast Agent Chemical Drug 18F-(2S,4R)-4-fluoroglutamine; 18F-fluorodeoxyglucose
Contrast Agent Dose 4.32 ± 0.23MBq; 4.46 ± 0.41 MBq
Injection Volume 0,03
Injection Time scanning 15 and 60 minutes from tracer injection
Vehicle saline
Route Of Administration intravenous
Cell Line Vk12598 cells (cell line 1); JJN3 HMCL cells (cell line 2)
Provenance Leibniz Institute Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (Braunschweig,Germany) and from Vk*MYC transgenic mouse
Cell Injection Route Vk12598 cells: i.v.; JJN3 HMCL cells: subcutaneous
Number Of Cells 0.5 × 10^6 for cell line 1; 5 × 10^6 for cell line 2
Image Acquisition
Instrument Vendor ISE s.r.l.
Instrument Type YAP-(S)-PET II
Instrument Specifics PET: FOV of 40x40 mm
Image Acquisition Parameters PET: 511 KeV, 30% energy resolution.
Correction PET: isotope decay and random coincidences correction
Raw Data Yes
Qa Qc Yes. Annual QC
Image Correlation
Image Type Reconstructed and quantified images
Image Scale KBq/cc for PET
Format Compression raw, DICOM
Dimensions 3D
Overall Number Of Images 1 dataset per animal per time point
Field Of View Max FOV for PET
Dimension Extents 128 x 128 x 27
Size Description 40 x 40 x 40 mm
Pixel Voxel Size Description 0,3125 x 0,3125 x 1,5 mm
Image Reconstruction Algorithm PET: EM (30 iterations)
Quality Control no
Image Registration Algorithm no
Ai Enhanced Algorithm no
Corrections PET: acquisition decay, randoms
Spatial And Temporal Alignment no
Coregistered Images no
Analyzed Data
Analysis Result Type regional increase of radiotracer's uptake
Data Used For Analysis VOIs analysis, SUV
Analysis Method And Details PMOD
Status complete
Ontology Terms
Ncit Imaging NCIT:C17007
Doid DOID:9538
Ncit Species NCIT:C14238
Ncit Strain NCIT:C15167
Chebi Pharmaco CHEBI:52717
Chebi Anesthesia CHEBI:6015
Chebi Contrast Agent Commercial Name CHEBI:49134
Chebi Contrast Agent Chemical Name CHEBI:49134
Clo CLO_0037173
Back to List