Evidence map›Paper›PMID 19223408›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2009

Quantification of tryptophan transport and metabolism in lung tumors using PET.

Csaba Juhász, Otto Muzik, Xin Lu, M Salik Jahania, Ayman O Soubani, Majid Khalaf, Fangyu Peng, Thomas J Mangner, Pulak K Chakraborty, Diane C Chugani

Open access · bronzeAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Radiopharmaceuticals and their applications in medicine.Signal transduction and targeted therapy · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Evaluation of L-1-[Molecular imaging and biology · 2019
    Article
  7. Review
  8. Metabolic signatures of four major histological types of lung cancer cells.Metabolomics : Official journal of the Metabolomic Society · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 1-butyltryptophan inhibits cell proliferation, migration, and invasion through the Akt pathway in human gastric cancer cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Molecular imaging and targeted therapies.Biochemical pharmacology · 2010
    Review
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

10 authors at 1 institution in 1 country.

Csaba JuhászPET Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan, USA. juhasz@pet.wayne.edu
Otto Muzik
Xin Lu
M Salik Jahania
Ayman O Soubani
Majid Khalaf
Fangyu Peng
Thomas J Mangner
Pulak K Chakraborty
Diane C Chugani
Wayne State University · US

Funding

Tryptophan Metabolism in Human Brain TumorsR01CA123451 · NCI · WAYNE STATE UNIVERSITY · PI JUHASZ, CSABA, MITTAL, SANDEEP · 2008 to 2018
$3.1M
NCI NIH HHS CA-12341NCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400NCI NIH HHS R01 CA123451
6 · The paper itself

Abstract

unlabelledAbnormal tryptophan metabolism catalyzed by indoleamine 2,3-dioxygenase may play a prominent role in tumor immunoresistance in many tumor types, including lung tumors. The goal of this study was to evaluate the in vivo kinetics of alpha-(11)C-methyl-l-tryptophan (AMT), a PET tracer for tryptophan metabolism, in human lung tumors.

methodsTracer transport and metabolic rates were evaluated in 18 lesions of 10 patients using dynamic PET/CT with AMT. The kinetic values were compared between tumors and unaffected lung tissue, tested against a simplified analytic approach requiring no arterial blood sampling, and correlated with standardized uptake values (SUVs) obtained from (18)F-FDG PET/CT scans.

resultsMost non-small cell lung cancers (NSCLCs) showed prolonged retention of AMT, but 3 other lesions (2 benign lesions and a rectal cancer metastasis) and unaffected lung tissue showed no such retention. Transport and metabolic rates of AMT were substantially higher in NSCLCs than in the other tumors and unaffected lung tissue. A simplified analytic approach provided an excellent estimate of transport rates but only suboptimal approximation of tryptophan metabolic rates. (18)F-FDG SUVs showed a positive correlation with AMT uptake, suggesting higher tryptophan transport and metabolism in tumors with higher proliferation rates.

conclusionProlonged retention of AMT in NSCLCs suggests high metabolic rates of tryptophan in these tumors. AMT PET/CT may be a clinically useful molecular imaging method for personalized cancer treatment by identifying and monitoring patients who have increased tumor tryptophan metabolism and are potentially sensitive to immunopharmacotherapy with indoleamine 2,3-dioxygenase inhibitors.

Indexed as

AdultAgedCarcinoma, Non-Small-Cell LungFeasibility StudiesFemaleFluorodeoxyglucose F18HumansLung NeoplasmsMaleMiddle AgedPilot ProjectsPositron-Emission TomographyRadiopharmaceuticalsRectal NeoplasmsTryptophanalpha-methyltryptophanFluorodeoxyglucose F18RadiopharmaceuticalsTryptophan

Identifiers

PMID19223408
PMCPMC2784997
OpenAlexW2124533699

What OpenQuestion holds

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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.