Evidence map›Paper›PMID 40826308›Full record

ArticleMolecular imaging and biology2025

Enhanced Visualisation of Colorectal Tumours via Topical Application of EMI-137 in a Methylcellulose-Based Formulation: An ex vivo Feasibility Study.

Elham Zonoobi, Daan G J Linders, Stefan Harmsen, María Rita Rodríguez Luna, Shadhvi S Bhairosingh, Dima D A Almandawi, Ronald L P Van Vlierberghe, Marvin W J Nogaitzig, Christophe Portal, Stijn A L P Crobach and 9 more

Abstract read
In one paragraph

Article in Molecular imaging and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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.

No citing paper in PubMed yet.

4 · The record

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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

19 authors.

Elham ZonoobiDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.ORCID 0000-0002-0163-8423
Daan G J LindersDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Stefan HarmsenDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
María Rita Rodríguez LunaHospital de Barcelona, Av. Diagonal, 660, Les Corts, 08034, Barcelona, Spain.
Shadhvi S BhairosinghDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Dima D A AlmandawiDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Ronald L P Van VlierbergheDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Marvin W J NogaitzigDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Christophe PortalEdinburgh Molecular Imaging Limited. Nine Edinburgh Bioquarter, 9 Little France Road, Edinburgh, EH16 4UX, UK.
Stijn A L P CrobachDepartment of Pathology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Michele DianaICube Lab, Photonics Instrumentation for Health, 300 Bd Sébastien Brant, 67400, Illkirch-Graffenstaden, France.
Gilbert NoordamDepartement of Pathology, Haaglanden Medisch Centrum, The Hague, 2512 VA, The Netherlands.
Davey van den BurgDepartement of Pathology, Haaglanden Medisch Centrum, The Hague, 2512 VA, The Netherlands.
Elke E M PetersDepartement of Pathology, Haaglanden Medisch Centrum, The Hague, 2512 VA, The Netherlands.
Andreas W K S MarinelliDepartment of Surgery, Haaglanden Medisch Centrum, The Hague, 2512 VA, The Netherlands.
Rob A E M TollenaarDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Denise E HillingDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Peter J K KuppenDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Alexander L VahrmeijerDepartment of Surgery, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands. a.l.vahrmeijer@lumc.nl.

Funding

H2020 Marie Skłodowska-Curie Actions 857894-CAST
6 · The paper itself

Abstract

backgroundFluorescence-guided molecular imaging may improve colorectal cancer (CRC) patient outcomes by enabling early detection and better surgical treatment, relying on developing targeted fluorescent tracers to highlight tumours. This study investigates visualising primary colon tumours by topically applying EMI-137, a targeted fluorescent tracer designed to bind to c-Met receptor. We introduce a novel viscous formulation to enhance the tracer's performance, aiming for a clear, robust fluorescent signal by improving contact with mucosal surface of ex vivo colon specimens.

methodsWe evaluated fluorescence properties of EMI-137 in phosphate-buffered saline (PBS) and in methylcellulose (m-cellulose) and determined emission spectrum of the tracer in both formulations. Flow cytometry was used to determine EMI-137's specificity for c-Met receptor and its optimal concentration. Live-cell imaging visually confirmed EMI-137's fluorescence signal for the c-Met receptor, highlighting its distinctive characteristics across various solvents. In a prospective cohort study, freshly excised colon cancer specimens were incubated with EMI-137 in PBS or m-cellulose. Specimens underwent a meticulous washing process. Near-infrared fluorescence imaging was performed and compared with histopathological analysis to validate detection accuracy.

resultsFluorospectrometry showed that m-cellulose enhanced EMI-137's fluorescence intensity compared to PBS. Flow cytometry showed dose-dependent binding of EMI-137 in HT-29 cells, with an optimum at 500 nM. Microscopy confirmed targeting of c-Met receptors. Topical EMI-137 dissolved in m-cellulose visualised colon tumours effectively, resulting in a high tumour-to-background ratio. Histopathological analysis confirmed c-Met expression in these colon tumours.

conclusionEMI-137 in a novel viscous vehicle effectively imaged c-Met expressing colon tumors, potentially facilitating fluorescent-guided tumor imaging.

Indexed as

Colorectal NeoplasmsMethylcelluloseAdministration, TopicalFeasibility StudiesHumansOptical ImagingProto-Oncogene Proteins c-metMethylcelluloseProto-Oncogene Proteins c-metc-Met receptorColorectal cancerFluorescenceFormulationsMolecular imagingTopical application

Identifiers

PMID40826308
PMCPMC12628436

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