Evidence map›Paper›PMID 30036545›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2018

Quantitative imaging of receptor-ligand engagement in intact live animals.

Alena Rudkouskaya, Nattawut Sinsuebphon, Jamie Ward, Kate Tubbesing, Xavier Intes, Margarida Barroso

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
  7. bioRxiv : the preprint server for biology · 2023
    Article
  8. Visualizing cell-cell communication using synthetic notch activated MRI.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Optica · 2022
    Article
  10. Article
  11. Deep learning in macroscopic diffuse optical imaging.Journal of biomedical optics · 2022
    Review
  12. Article
  13. Deep Learning in Biomedical Optics.Lasers in surgery and medicine · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 2 institutions in 1 country.

Alena RudkouskayaDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.
Nattawut SinsuebphonDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.
Jamie WardDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.
Kate TubbesingDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.
Xavier IntesDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA. Electronic address: intesx@rpi.edu.
Margarida BarrosoDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA. Electronic address: barrosm@amc.edu.
Albany Medical Center Hospital · USRensselaer Polytechnic Institute · US

Funding

Role of tumor heterogeneity on receptor engagementR01CA207725 · NCI · RENSSELAER POLYTECHNIC INSTITUTE · PI BARROSO, MARGARIDA, CORR, DAVID THOMAS · 2017 to 2021
$3.0M
Time-Resolved Wide-Field Molecular Optical TomographyR01EB019443 · NIBIB · RENSSELAER POLYTECHNIC INSTITUTE · PI INTES, XAVIER · 2015 to 2018
$1.7M
NCI NIH HHS R01 CA207725NIBIB NIH HHS R01 EB019443
6 · The paper itself

Abstract

Maintaining an intact tumor environment is critical for quantitation of receptor-ligand engagement in a targeted drug development pipeline. However, measuring receptor-ligand engagement in vivo and non-invasively in preclinical settings is extremely challenging. We found that quantitation of intracellular receptor-ligand binding can be achieved using whole-body macroscopic lifetime-based Förster Resonance Energy Transfer (FRET) imaging in intact, live animals bearing tumor xenografts. We determined that FRET levels report on ligand binding to transferrin receptors conversely to raw fluorescence intensity. FRET levels in heterogeneous tumors correlate with intracellular ligand binding but strikingly, not with ubiquitously used ex vivo receptor expression assessment. Hence, MFLI-FRET provides a direct measurement of systemic delivery, target availability and intracellular drug delivery in preclinical studies. Here, we have used MFLI to measure FRET longitudinally in intact and live animals. MFLI-FRET is well-suited for guiding the development of targeted drug therapy in heterogeneous tumors in intact, live small animals.

Indexed as

Drug Delivery SystemsAnimalsAntineoplastic AgentsCell Line, TumorEquipment DesignFemaleFluorescence Resonance Energy TransferFluorescent DyesHumansMice, NudeNeoplasmsOptical ImagingReceptors, TransferrinTransferrinWhole Body ImagingAntineoplastic AgentsFluorescent DyesReceptors, TransferrinTransferrinFRETLifetimeOptical imagingTarget engagementTransferrinTumor xenograft

Identifiers

PMID30036545
PMCPMC6231501
OpenAlexW2949309783

What OpenQuestion holds

Textmetadata
LicenceTDM
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.