Evidence map›Paper›PMID 26252891›Full record

ArticlePloS one2015

Multimodal Imaging of Orthotopic Mouse Model of Endometrial Carcinoma.

Ingfrid S Haldorsen, Mihaela Popa, Tina Fonnes, Njål Brekke, Reidun Kopperud, Nicole C Visser, Cecilie B Rygh, Tina Pavlin, Helga B Salvesen, Emmet McCormack and 1 more

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Patient-Derived Xenograft Models in Cervical Cancer: A Systematic Review.International journal of molecular sciences · 2021
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  13. Feasibility and utility of MRI and dynamicJournal of translational medicine · 2021
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  17. Establishment of a [Journal of gastric cancer · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ingfrid S HaldorsenDepartment of Radiology, Haukeland University Hospital, Bergen, Norway; Section for Radiology, Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Mihaela PopaDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Tina FonnesCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Njål BrekkePET-centre, Department of Radiology, Haukeland University Hospital, Bergen, Norway.
Reidun KopperudCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Nicole C VisserDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Cecilie B RyghMolecular Imaging Center, Department of Biomedicine, University of Bergen, Bergen, Norway.
Tina PavlinMolecular Imaging Center, Department of Biomedicine, University of Bergen, Bergen, Norway.
Helga B SalvesenCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway; Department of Obstetrics and Gynaecology, Haukeland University Hospital, Bergen, Norway.
Emmet McCormackDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Camilla KrakstadCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway; Department of Obstetrics and Gynaecology, Haukeland University Hospital, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOrthotopic endometrial cancer models provide a unique tool for studies of tumour growth and metastatic spread. Novel preclinical imaging methods also have the potential to quantify functional tumour characteristics in vivo, with potential relevance for monitoring response to therapy.

methodsAfter orthotopic injection with luc-expressing endometrial cancer cells, eleven mice developed disease detected by weekly bioluminescence imaging (BLI). In parallel the same mice underwent positron emission tomography-computed tomography (PET-CT) and magnetic resonance imaging (MRI) employing 18F-fluorodeoxyglocose (18F-FDG) or 18F- fluorothymidine (18F-FLT) and contrast reagent, respectively. The mice were sacrificed when moribund, and post-mortem examination included macroscopic and microscopic examination for validation of growth of primary uterine tumours and metastases. PET-CT was also performed on a patient derived model (PDX) generated from a patient with grade 3 endometrioid endometrial cancer.

resultsIncreased BLI signal during tumour growth was accompanied by increasing metabolic tumour volume (MTV) and increasing MTV x mean standard uptake value of the tumour (SUVmean) in 18F-FDG and 18F-FLT PET-CT, and MRI conspicuously depicted the uterine tumour. At necropsy 82% (9/11) of the mice developed metastases detected by the applied imaging methods. 18F-FDG PET proved to be a good imaging method for detection of patient derived tumour tissue.

conclusionsWe demonstrate that all imaging modalities enable monitoring of tumour growth and metastatic spread in an orthotopic mouse model of endometrial carcinoma. Both PET tracers, 18F-FDG and 18F-FLT, appear to be equally feasible for detecting tumour development and represent, together with MRI, promising imaging tools for monitoring of patient-derived xenograft (PDX) cancer models.

Indexed as

Multimodal ImagingAgedAnimalsCarcinomaCell Line, TumorContrast MediaDideoxynucleosidesDisease Models, AnimalDisease ProgressionEndometrial NeoplasmsFemaleFluorodeoxyglucose F18HumansMiceMice, Inbred NODMice, SCIDalovudineContrast MediaDideoxynucleosidesFluorodeoxyglucose F18

Identifiers

PMID26252891
PMCPMC4529312

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.