Evidence map›Paper›PMID 22138753›Full record

ArticleNature medicine2011

In vivo imaging of ligand receptor binding with Gaussia luciferase complementation.

Kathryn E Luker, Laura Anne Mihalko, Bradley T Schmidt, Sarah A Lewin, Paramita Ray, Dmitry Shcherbo, Dmitriy M Chudakov, Gary D Luker

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 69 citations in OpenAlex.

  1. A high-throughputActa pharmaceutica Sinica. B · 2023
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  8. Molecular Imaging with Reporter Genes: Has Its Promise Been Delivered?Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Dual Reporter Bioluminescence Imaging with NanoLuc and Firefly Luciferase.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  14. Article
  15. New imaging probes to track cell fate: reporter genes in stem cell research.Cellular and molecular life sciences : CMLS · 2017
    Review
  16. Article
  17. Review
  18. Article
  19. Fluorescence Lifetime Imaging of Apoptosis.Tomography (Ann Arbor, Mich.) · 2015
    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

8 authors at 2 institutions in 2 countries.

Kathryn E LukerCenter for Molecular Imaging, Department of Radiology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Laura Anne Mihalko
Bradley T Schmidt
Sarah A Lewin
Paramita Ray
Dmitry Shcherbo
Dmitriy M Chudakov
Gary D Luker
University of Michigan–Ann Arbor · USPrivolzhsky Research Medical University · RU

Funding

Small Animal Imaging CoreP50CA093990 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSS, BRIAN D. · 2002 to 2012
$19.0M
Targeted Multi-Spectral Dual Axes Confocal Imaging of In Vivo Molecular ExpressioR01CA142750 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KURABAYASHI, KATSUO, LUKER, GARY D · 2010 to 2014
$2.4M
Microfluidic Models of Metastatic CancerR01CA136829 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKER, GARY D · 2009 to 2013
$1.5M
Molecular Imaging of Chemokine Receptor SignalingR01CA136553 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKER, GARY D · 2009 to 2013
$1.5M
Michigan Small Animal Imaging Resource (MSAIR)U24CA083099 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSS, BRIAN D. · 2007 to 2008
$1.3M
Olympus FV1000-MPE Confocal & Multi-Photon Imaging SystemS10RR028819 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKER, GARY D · 2010 to 2010
$940k
NCI NIH HHS P50 CA093990NCI NIH HHS P50 CA93990NCI NIH HHS R01 CA136553NCI NIH HHS R01 CA136829NCI NIH HHS R01 CA142750NCI NIH HHS U24 CA083099NCRR NIH HHS S10 RR028819
6 · The paper itself

Abstract

Studies of ligand-receptor binding and the development of receptor antagonists would benefit greatly from imaging techniques that translate directly from cell-based assays to living animals. We used Gaussia luciferase protein fragment complementation to quantify the binding of chemokine (C-X-C motif) ligand 12 (CXCL12) to chemokine (C-X-C motif) receptor 4 (CXCR4) and CXCR7. Studies established that small-molecule inhibitors of CXCR4 or CXCR7 specifically blocked CXCL12 binding in cell-based assays and revealed differences in kinetics of inhibiting chemokine binding to each receptor. Bioluminescence imaging showed CXCL12-CXCR7 binding in primary and metastatic tumors in a mouse model of breast cancer. We used this imaging technique to quantify drug-mediated inhibition of CXCL12-CXCR4 binding in living mice. We expect this imaging technology to advance research in areas such as ligand-receptor interactions and the development of new therapeutic agents in cell-based assays and small animals.

Indexed as

AnimalsBenzylaminesBreast NeoplasmsCell Line, TumorChemokine CXCL12CyclamsFemaleHEK293 CellsHeterocyclic CompoundsHumansLigandsLuciferasesLuminescent MeasurementsMiceMolecular ImagingNeoplasms, ExperimentalBenzylaminesChemokine CXCL12CyclamsHeterocyclic CompoundsLigandsLuciferasesplerixaforReceptors, CXCRReceptors, CXCR4

Identifiers

PMID22138753
PMCPMC3253890
OpenAlexW2086341539

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.