Evidence map›Paper›PMID 19768136›Full record

ArticleCurrent medical imaging reviews2009

In Vivo Cellular Imaging for Translational Medical Research.

Ali S Arbab, Branislava Janic, Jodi Haller, Edyta Pawelczyk, Wei Liu, Joseph A Frank

Open access · bronzeAbstract read
In one paragraph

Article in Current medical imaging reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Clinical imaging in regenerative medicine.Nature biotechnology · 2014
    Review
  17. Article
  18. Review
  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 3 institutions in 1 country.

Ali S ArbabCellular and Molecular Imaging Laboratory, Department of Radiology, Henry Ford Hospital, Detroit, MI.
Branislava Janic
Jodi Haller
Edyta Pawelczyk
Wei Liu
Joseph A Frank
Henry Ford Hospital · USNational Institutes of Health · USNational Institutes of Health Clinical Center · US

Funding

Cellular MRI in Glioma and Radiation NecrosisR01CA122031 · NCI · HENRY FORD HEALTH SYSTEM · PI ARBAB, ALI SYED · 2007 to 2010
$992k
Stem Cells as Delivery Vehicles and Imaging Probes for Glioma Gene TherapyR21CA129801 · NCI · HENRY FORD HEALTH SYSTEM · PI ARBAB, ALI SYED · 2008 to 2009
$359k
Differentiation of Glioma from Radiation Injury Using Cellular MRIR21NS058589 · NINDS · HENRY FORD HEALTH SYSTEM · PI ARBAB, ALI SYED · 2007 to 2008
$349k
Pre-clinical evaluation of Magnetically labeled Cells for Cellular MRIZIACL090007 · CLC · CLINICAL CENTER · PI FRANK, JOSEPH · 2009 to 2018
$0k
NCI NIH HHS R01 CA122031NCI NIH HHS R21 CA129801NINDS NIH HHS R21 NS058589
6 · The paper itself

Abstract

Personalized treatment using stem, modified or genetically engineered, cells is becoming a reality in the field of medicine, in which allogenic or autologous cells can be used for treatment and possibly for early diagnosis of diseases. Hematopoietic, stromal and organ specific stem cells are under evaluation for cell-based therapies for cardiac, neurological, autoimmune and other disorders. Cytotoxic or genetically altered T-cells are under clinical trial for the treatment of hematopoietic or other malignant diseases. Before using stem cells in clinical trials, translational research in experimental animal models are essential, with a critical emphasis on developing noninvasive methods for tracking the temporal and spatial homing of these cells to target tissues. Moreover, it is necessary to determine the transplanted cell's engraftment efficiency and functional capability. Various in vivo imaging modalities are in use to track the movement and incorporation of administered cells. Tagging cells with reporter genes, fluorescent dyes or different contrast agents transforms them into cellular probes or imaging agents. Recent reports have shown that magnetically labeled cells can be used as cellular magnetic resonance imaging (MRI) probes, demonstrating the cell trafficking to target tissues. In this review, we will discuss the methods to transform cells into probes for in vivo imaging, along with their advantages and disadvantages as well as the future clinical applicability of cellular imaging method and corresponding imaging modality.

Identifiers

PMID19768136
PMCPMC2746660
OpenAlexW1968796538

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.