Evidence map›Paper›PMID 27491535›Full record

ArticleScientific reports2016

The use of thermographic imaging to evaluate therapeutic response in human tumour xenograft models.

Nosheen Hussain, David Connah, Hassan Ugail, Patricia A Cooper, Robert A Falconer, Laurence H Patterson, Steven D Shnyder

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Refinement in the European Union: A Systematic Review.Animals : an open access journal from MDPI · 2022
    Review
  4. Article
  5. Article
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

7 authors.

Nosheen HussainUniversity of Bradford, Institute of Cancer Therapeutics, Bradford BD7 1DP, United Kingdom.
David ConnahUniversity of Bradford, Centre for Visual Computing, Bradford BD7 1DP, United Kingdom.
Hassan UgailUniversity of Bradford, Centre for Visual Computing, Bradford BD7 1DP, United Kingdom.
Patricia A CooperUniversity of Bradford, Institute of Cancer Therapeutics, Bradford BD7 1DP, United Kingdom.
Robert A FalconerUniversity of Bradford, Institute of Cancer Therapeutics, Bradford BD7 1DP, United Kingdom.
Laurence H PattersonUniversity of Bradford, Institute of Cancer Therapeutics, Bradford BD7 1DP, United Kingdom.
Steven D ShnyderUniversity of Bradford, Institute of Cancer Therapeutics, Bradford BD7 1DP, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-invasive methods to monitor tumour growth are an important goal in cancer drug development. Thermographic imaging systems offer potential in this area, since a change in temperature is known to be induced due to changes within the tumour microenvironment. This study demonstrates that this imaging modality can be applied to a broad range of tumour xenografts and also, for the first time, the methodology's suitability to assess anti-cancer agent efficacy. Mice bearing subcutaneously implanted H460 lung cancer xenografts were treated with a novel vascular disrupting agent, ICT-2552, and the cytotoxin doxorubicin. The effects on tumour temperature were assessed using thermographic imaging over the first 6 hours post-administration and subsequently a further 7 days. For ICT-2552 a significant initial temperature drop was observed, whilst for both agents a significant temperature drop was seen compared to controls over the longer time period. Thus thermographic imaging can detect functional differences (manifesting as temperature reductions) in the tumour response to these anti-cancer agents compared to controls. Importantly, these effects can be detected in the first few hours following treatment and therefore the tumour is observable non-invasively. As discussed, this technique will have considerable 3Rs benefits in terms of reduction and refinement of animal use.

Indexed as

ThermographyXenograft Model Antitumor AssaysAnimalsAnimal Use AlternativesDoxorubicinHumansMiceNeoplasmsOligopeptidesThioureaDoxorubicinICT 2552OligopeptidesThiourea

Identifiers

PMID27491535
PMCPMC4974555

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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.