Evidence map›Paper›PMID 30718557›Full record

ArticleScientific reports2019

A step towards valid detection and quantification of lung cancer volume in experimental mice with contrast agent-based X-ray microtomography.

Pidassa Bidola, Juliana Martins de Souza E Silva, Klaus Achterhold, Enkhtsetseg Munkhbaatar, Philipp J Jost, Anna-Lena Meinhardt, Kirsten Taphorn, Marie-Christine Zdora, Franz Pfeiffer, Julia Herzen

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–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

16 citing papers in PubMed.

  1. Review
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  9. X-ray Stain Localization with Near-Field Ptychographic Computed Tomography.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
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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

10 authors.

Pidassa BidolaDepartment of Physics & Munich School of Bioengineering, Technical University of Munich, 85748, Garching, Germany.
Juliana Martins de Souza E SilvaDepartment of Physics & Munich School of Bioengineering, Technical University of Munich, 85748, Garching, Germany. juliana.martins@physik.uni-halle.de.
Klaus AchterholdDepartment of Physics & Munich School of Bioengineering, Technical University of Munich, 85748, Garching, Germany.ORCID 0000-0002-8724-1637
Enkhtsetseg MunkhbaatarIII. Medizinische Klinik, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.
Philipp J JostIII. Medizinische Klinik, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.ORCID 0000-0003-2454-0362
Anna-Lena MeinhardtIII. Medizinische Klinik, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.
Kirsten TaphornDepartment of Physics & Munich School of Bioengineering, Technical University of Munich, 85748, Garching, Germany.
Marie-Christine ZdoraDiamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire, OX11 0DE, United Kingdom.ORCID 0000-0001-6953-6709
Franz PfeifferDepartment of Physics & Munich School of Bioengineering, Technical University of Munich, 85748, Garching, Germany.
Julia HerzenDepartment of Physics & Munich School of Bioengineering, Technical University of Munich, 85748, Garching, Germany.ORCID 0000-0002-9456-1591

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor volume is a parameter used to evaluate the performance of new therapies in lung cancer research. Conventional methods that are used to estimate tumor size in mouse models fail to provide fast and reliable volumetric data for tumors grown non-subcutaneously. Here, we evaluated the use of iodine-staining combined with micro-computed tomography (micro-CT) to estimate the tumor volume of ex vivo tumor-burdened lungs. We obtained fast high spatial resolution three-dimensional information of the lungs, and we demonstrated that iodine-staining highlights tumors and unhealthy tissue. We processed iodine-stained lungs for histopathological analysis with routine hematoxylin and eosin (H&E) staining. We compared the traditional tumor burden estimation performed manually with H&E histological slices with a semi-automated method using micro-CT datasets. In mouse models that develop lung tumors with well precise boundaries, the method that we describe here enables to perform a quick estimation of tumorous tissue volume in micro-CT images. Our method overestimates the tumor burden in tumors surrounded by abnormal tissue, while traditional histopathological analysis underestimates tumor volume. We propose to embed micro-CT imaging to the traditional workflow of tumorous lung analyses in preclinical cancer research as a strategy to obtain a more accurate estimation of the total lung tumor burden.

Indexed as

Tumor BurdenAnimalsContrast MediaDisease Models, AnimalHumansLungLung NeoplasmsMiceX-Ray MicrotomographyContrast Media

Identifiers

PMID30718557
PMCPMC6362109

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Registered trials

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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.