Evidence map›Paper›PMID 30305717›Full record

ArticleScientific reports2018

Non-invasive imaging of disrupted protein homeostasis induced by proteasome inhibitor treatment using chemical exchange saturation transfer MRI.

Yanan Zhu, Rajiv Ramasawmy, Sean Peter Johnson, Valerie Taylor, Alasdair Gibb, R Barbara Pedley, Nibedita Chattopadhyay, Mark F Lythgoe, Xavier Golay, Daniel Bradley and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% of its field
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 2 countries.

Yanan ZhuCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, United Kingdom.
Rajiv RamasawmyCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, United Kingdom.
Sean Peter JohnsonCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, United Kingdom.
Valerie TaylorCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, United Kingdom.
Alasdair GibbNeuroscience, Physiology & Pharmacology, University College London, London, WC1E 6BT, United Kingdom.
R Barbara PedleyCancer Institute, University College London, London, WC1E 6DD, United Kingdom.
Nibedita ChattopadhyayCancer Pharmacology, Takeda Pharmaceutical International Corporation, Cambridge, MA, 02139, United States.
Mark F LythgoeCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, United Kingdom.
Xavier GolayInstitute of Neurology, University College London, London, WC1N 3BG, United Kingdom.ORCID http://orcid.org/0000-0002-6447-4446
Daniel BradleyBiomedical Imaging Group, Takeda Pharmaceutical International Corporation, Cambridge, MA, 02139, United States.
Simon Walker-SamuelCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, United Kingdom. simon.walkersamuel@ucl.ac.uk.ORCID http://orcid.org/0000-0003-3530-9166
University College London · GBTakeda (United States) · US

Funding

Cancer Research UK 16463Wellcome Trust WT100247MA
6 · The paper itself

Abstract

Proteasome inhibitors (PIs) are now standard of care for several cancers, and noninvasive biomarkers of treatment response are critically required for early patient stratification and treatment personalization. The present study evaluated whether chemical exchange (CEST) magnetic resonance imaging (MRI) can provide measurements that can be used as the noninvasive biomarkers of proteasome inhibition, alongside diffusion MRI and relaxometry. The sensitivity of human colorectal carcinoma cells to the PI Ixazomib was assessed via in vitro and in vivo dose-response experiments. Acute in vivo response to Ixazomib was assessed at three dosing concentrations, using CEST MRI (amide, amine, hydroxyl signals), diffusion MRI (ADC) and relaxometry (T

Indexed as

Magnetic Resonance ImagingAmidesAminesAnimalsApoptosisBoron CompoundsCell Line, TumorCell SurvivalColorectal NeoplasmsDiffusion Magnetic Resonance ImagingDose-Response Relationship, DrugFemaleGlycineHumansImage Interpretation, Computer-AssistedMice, NudeAmidesAminesBoron CompoundsGlycineixazomibProteasome Inhibitors

Identifiers

PMID30305717
PMCPMC6180115
OpenAlexW2895226912

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.