Evidence map›Paper›PMID 29737435›Full record

ArticleMagma (New York, N.Y.)2018

Anti-EpCAM scFv gadolinium chelate: a novel targeted MRI contrast agent for imaging of colorectal cancer.

Kannika Khantasup, Pairash Saiviroonporn, Suwatchai Jarussophon, Warangkana Chantima, Tararaj Dharakul

Abstract read
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In one paragraph

Article in Magma (New York, N.Y.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 55% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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

5 authors at 2 institutions in 1 country.

Kannika KhantasupResearch Division, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Pairash SaiviroonpornDepartment of Radiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Suwatchai JarussophonNational Nanotechnology Center, National Science and Technology Development Agency, Pathum Thani, Thailand.
Warangkana ChantimaGraduate Program in Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Tararaj DharakulNANOTEC-Mahidol University Center of Excellence in Nanotechnology for Cancer Diagnosis and Treatment, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. tararaj.dha@mahidol.ac.th.ORCID http://orcid.org/0000-0002-5602-0778
Siriraj Hospital · THNational Science and Technology Development Agency · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe development of targeted contrast agents for magnetic resonance imaging (MRI) facilitates enhanced cancer imaging and more accurate diagnosis. In the present study, a novel contrast agent was developed by conjugating anti-EpCAM humanized scFv with gadolinium chelate to achieve target specificity. MATERIALS AND

methodsThe material design strategy involved site-specific conjugation of the chelating agent to scFv. The scFv monomer was linked to maleimide-DTPA via unpaired cysteine at the scFv C-terminus, followed by chelation with gadolinium (Gd). Successful scFv-DTPA conjugation was achieved at 1:10 molar ratio of scFv to maleimide-DTPA at pH 6.5. The developed anti-EpCAM-Gd-DTPA MRI contrast agent was evaluated for cell targeting ability, in vitro serum stability, cell cytotoxicity, relaxivity, and MR contrast enhancement.

resultsA high level of targeting efficacy of anti-EpCAM-Gd-DTPA to an EpCAM-overexpressing HT29 colorectal cell was demonstrated by confocal microscopy. Good stability of the contrast agent was obtained and no cytotoxicity was observed in HT29 cells after 48 h incubation with 25-100 µM of Gd. Favorable imaging was obtained using anti-EpCAM-Gd-DTPA, including 1.8-fold enhanced relaxivity compared with Gd-DTPA, and MR contrast enhancement observed after binding to HT29.

conclusionThe potential benefit of this contrast agent for in vivo MR imaging of colorectal cancer, as well as other EpCAM positive cancers, is suggested and warrants further investigation.

Indexed as

Binding SitesCell Line, TumorChelating AgentsColorectal NeoplasmsContrast MediaDose-Response Relationship, DrugEpithelial Cell Adhesion MoleculeGadoliniumGadolinium DTPAHEK293 CellsHumansImmunoglobulin FragmentsMagnetic Resonance ImagingMaleimidesMicroscopy, ConfocalProtein DomainsChelating AgentsContrast MediaEPCAM protein, humanEpithelial Cell Adhesion MoleculeGadoliniumGadolinium DTPAImmunoglobulin FragmentsmaleimideMaleimidesGadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA)Human epithelial cell adhesion molecule (EpCAM)Humanized scFvMagnetic resonance imaging (MRI)

Identifiers

PMID29737435
OpenAlexW2802867384

What OpenQuestion holds

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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.