Evidence map›Paper›PMID 19265438›Full record

ReviewAccounts of chemical research2009

Responsive MRI agents for sensing metabolism in vivo.

Luis M De Leon-Rodriguez, Angelo Josue M Lubag, Craig R Malloy, Gary V Martinez, Robert J Gillies, A Dean Sherry

Abstract readReview
In one paragraph

Review in Accounts of chemical research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
–field-weighted citation impact
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

71 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. MRI Contrast Agents in Glycobiology.Molecules (Basel, Switzerland) · 2022
    Review
  9. Towards Photoswitchable Contrast Agents for Absolute 3D Temperature MR Imaging.Angewandte Chemie (International ed. in English) · 2021
    Article
  10. Article
  11. Molecular Magnetic Resonance Imaging Using a Redox-Active Iron Complex.Journal of the American Chemical Society · 2019
    Article
  12. Article
  13. Review
  14. Design and synthesis of magnetic nanoparticles for biomedical diagnostics.Quantitative imaging in medicine and surgery · 2018
    Review
  15. Article
  16. Methods of Measuring Enzyme Activity Ex Vivo and In Vivo.Annual review of analytical chemistry (Palo Alto, Calif.) · 2018
    Review
  17. Recent development of nanoparticles for molecular imaging.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2017
    Review
  18. Article
  19. Article
  20. Article

11 more citing papers are in PubMed but not listed here.

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.

Luis M De Leon-RodriguezAdvanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.
Angelo Josue M Lubag
Craig R Malloy
Gary V Martinez
Robert J Gillies
A Dean Sherry

Funding

TARGETED RESPONSIVE MR AND PET AGENTS FOR B-CELL IMAGINGP01DK058398 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MUOIO, DEBORAH M · 2000 to 2016
$26.1M
YTTRIUM HYPERPOLARIZATIONP41RR002584 · NCRR · UT SOUTHWESTERN MEDICAL CENTER · PI MASON, RALPH P. · 1985 to 2011
$14.3M
The Physi(ologi)cal Microenvironment and its Role in Tumor Invasion and MetastaseU54CA143970 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI GATENBY, ROBERT A · 2009 to 2014
$9.3M
Causes & Consequences of Acid pH in TumorsR01CA077575 · NCI · UNIVERSITY OF ARIZONA · PI GILLIES, ROBERT J. · 1999 to 2018
$8.5M
PARACEST Agents: Optimization for Human MR ImagingR01EB004582 · NIBIB · UT SOUTHWESTERN MEDICAL CENTER · PI LENKINSKI, ROBERT E · 2006 to 2014
$7.5M
PARACEST AGENTS FOR MOLECULAR IMAGING OF CANCER BY MRIR01CA115531 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SHERRY, DEAN · 2005 to 2021
$4.2M
UT Southwestern Small Animal Imaging ResourceU24CA126608 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MASON, RALPH P., SHERRY, DEAN · 2007 to 2011
$2.3M
Imaging Biomarkers for Response to Anti-Cancer TherapyR01CA125627 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI BAKER, AMANDA F, GILLIES, ROBERT J. · 2008 to 2012
$1.7M
NCI NIH HHS CA-115531NCI NIH HHS CA-126608NCI NIH HHS R01 CA077575NCI NIH HHS R01 CA115531NCI NIH HHS R01 CA125627NCI NIH HHS U24 CA126608NCI NIH HHS U54 CA143970NCRR NIH HHS P41 RR002584NCRR NIH HHS RR-02584NIBIB NIH HHS EB-04582NIBIB NIH HHS R01 EB004582NIDDK NIH HHS DK-058398NIDDK NIH HHS P01 DK058398
6 · The paper itself

Abstract

Magnetic resonance imaging (MRI) has inherent advantages in safety, three-dimensional output, and clinical relevance when compared with optical and radiotracer imaging methods. However, MRI contrast agents are inherently less sensitive than agents used in other imaging modalities primarily because MRI agents are detected indirectly by changes in either the water proton relaxation rates (T(1), T(2), and T(*)(2)) or water proton intensities (chemical exchange saturation transfer and paramagnetic chemical exchange saturation transfer, CEST and PARACEST). Consequently, the detection limit of an MRI agent is determined by the characteristics of the background water signal; by contrast, optical and radiotracer-based methods permit direct detection of the agent itself. By virtue of responding to background water (which reflects bulk cell properties), however, MRI contrast agents have considerable advantages in "metabolic" imaging, that is, spatially resolving tissue variations in pH, redox state, oxygenation, or metabolite levels. In this Account, we begin by examining sensitivity limits in targeted contrast agents and then address contrast agents that respond to a physiological change; these responsive agents are effective metabolic imaging sensors. The sensitivity requirements for a metabolic imaging agent are quite different from those for a targeted Gd(3+)-based T(1) agent (for example, sensing cell receptors). Targeted Gd(3+) agents must have either an extraordinarily high water proton relaxivity (r(1)) or multiple Gd(3+) complexes clustered together at the target site on a polymer platform or nanoparticle assembly. Metabolic MRI agents differ in that the high relaxivity requirement, although helpful, is eased because these agents respond to bulk properties of tissues rather than low concentrations of a specific biological target. For optimal sensing, metabolic imaging agents should display a large change in relaxivity (deltar(1)) in response to the physiological or metabolic parameter of interest. Metabolic imaging agents have only recently begun to appear in the literature and only a few have been demonstrated in vivo. MRI maps of absolute tissue pH have been obtained with Gd(3+)-based T(1) sensors. The requirement of an independent measure of agent concentration in tissues complicates these experiments, but if qualitative changes in tissue pH are acceptable, then these agents can be quite useful. In this review, we describe examples of imaging extracellular pH in brain tumors, ischemic hearts, and pancreatic islets with Gd(3+)-based pH sensors and discuss the potential of CEST and PARACEST agents as metabolic imaging sensors.

Indexed as

Magnetic Resonance ImagingAnimalsBiosensing TechniquesBrain NeoplasmsContrast MediaGadoliniumMetabolomicsPeptoidsProtonsRadionuclide ImagingRatsContrast MediaGadoliniumPeptoidsProtons

Identifiers

PMID19265438
PMCPMC2713815

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.