Evidence map›Paper›PMID 25625022›Full record

ReviewAmerican journal of nuclear medicine and molecular imaging2015

The sweet spot: FDG and other 2-carbon glucose analogs for multi-modal metabolic imaging of tumor metabolism.

Benjamin L Cox, Thomas R Mackie, Kevin W Eliceiri

Open access · greenAbstract readReview
In one paragraph

Review in American journal of nuclear medicine and molecular imaging, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Application of Metabolic Reprogramming to Cancer Imaging and Diagnosis.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Disruption of Glucose Metabolism in AgedFrontiers in integrative neuroscience · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. eLife · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Nuclear Imaging of Glucose Metabolism: BeyondContrast media & molecular imaging · 2019
    Review
  16. Article
  17. The Potential of Metabolic Imaging.Seminars in nuclear medicine · 2016
    Review
  18. 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

3 authors at 1 institution in 1 country.

Benjamin L CoxDepartment of Medical Physics, University of Madison - Wisconsin 1111 Highland Ave, Madison, WI 53705 ; Medical Engineering Group, Morgridge Institute for Research 330 N Orchard St, Madison, WI 53715 ; Laboratory for Optical and Computational Instrumentation, University of Wisconsin - Madison 1675 Observatory Drive, Madison, WI 53706.
Thomas R MackieDepartment of Medical Physics, University of Madison - Wisconsin 1111 Highland Ave, Madison, WI 53705 ; Medical Engineering Group, Morgridge Institute for Research 330 N Orchard St, Madison, WI 53715 ; Laboratory for Optical and Computational Instrumentation, University of Wisconsin - Madison 1675 Observatory Drive, Madison, WI 53706.
Kevin W EliceiriDepartment of Medical Physics, University of Madison - Wisconsin 1111 Highland Ave, Madison, WI 53705 ; Medical Engineering Group, Morgridge Institute for Research 330 N Orchard St, Madison, WI 53715 ; Laboratory for Optical and Computational Instrumentation, University of Wisconsin - Madison 1675 Observatory Drive, Madison, WI 53706.
University of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multi-modal imaging approaches of tumor metabolism that provide improved specificity, physiological relevance and spatial resolution would improve diagnosing of tumors and evaluation of tumor progression. Currently, the molecular probe FDG, glucose fluorinated with (18)F at the 2-carbon, is the primary metabolic approach for clinical diagnostics with PET imaging. However, PET lacks the resolution necessary to yield intratumoral distributions of deoxyglucose, on the cellular level. Multi-modal imaging could elucidate this problem, but requires the development of new glucose analogs that are better suited for other imaging modalities. Several such analogs have been created and are reviewed here. Also reviewed are several multi-modal imaging studies that have been performed that attempt to shed light on the cellular distribution of glucose analogs within tumors. Some of these studies are performed in vitro, while others are performed in vivo, in an animal model. The results from these studies introduce a visualization gap between the in vitro and in vivo studies that, if solved, could enable the early detection of tumors, the high resolution monitoring of tumors during treatment, and the greater accuracy in assessment of different imaging agents.

Indexed as

deoxyglucoseFDGFDG-PETGlucoseglucose uptakemulti-modal imaging

Identifiers

PMID25625022
PMCPMC4299774
OpenAlexW270006814

What OpenQuestion holds

Textmetadata
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.