Evidence map›Paper›PMID 21666826›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2011

Stable isotope resolved metabolomics of lung cancer in a SCID mouse model.

Teresa W-M Fan, Andrew N Lane, Richard M Higashi, Jun Yan

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. NMR-Based Stable Isotope Tracing of Cancer Metabolism.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Cancer & metabolism · 2022
    Article
  14. Article
  15. NMR Analysis of Carboxylate Isotopomers ofAnalytical chemistry · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. NMR-Based Metabolomics.Advances in experimental medicine and biology · 2021
    Article
  20. Article

19 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

4 authors.

Teresa W-M FanDepartment of Chemistry, University of Louisville, 2210 S. Brook St, Rm 348 John W. Shumaker Research Building, Louisville, KY 40292, USA.
Andrew N Lane
Richard M Higashi
Jun Yan

Funding

PROJ 12: STEM CELL-BASED VACCINE FOR CANCER PROPHYLAXISP20RR018733 · NCRR · UNIVERSITY OF LOUISVILLE · PI TRENT, JOHN O · 2003 to 2011
$18.9M
TARGETING OF PHAGOCYTE &NK CELL CR3 TO TUMOR-BOUND IC3BR01CA086412 · NCI · UNIVERSITY OF LOUISVILLE · PI YAN, JUN · 2000 to 2009
$2.7M
Mechanisms of Immune Modulation Mediated by Yeast-derived Particulate Beta-GlucanR01CA150947 · NCI · UNIVERSITY OF LOUISVILLE · PI YAN, JUN · 2009 to 2012
$1.5M
Biochemical Mechanisms of Se Anticancer Activity in LungR01CA118434 · NCI · UNIVERSITY OF LOUISVILLE · PI FAN, TERESA WHEI-MEI · 2008 to 2011
$1.4M
Stable isotopomer analysis of anabolic metabolic pathways in breast cancerR21CA133668 · NCI · UNIVERSITY OF LOUISVILLE · PI LANE, ANDREW N. · 2009 to 2010
$358k
NCI NIH HHS R01 CA086412NCI NIH HHS R01 CA118434NCI NIH HHS R01 CA150947NCI NIH HHS R21 CA133668NCRR NIH HHS P20 RR018733
6 · The paper itself

Abstract

We have determined the time course of [U-(13)C]-glucose utilization and transformations in SCID mice via bolus injection of the tracer in the tail vein. Incorporation of (13)C into metabolites extracted from mouse blood plasma and several tissues (lung, heart, brain, liver, kidney, and skeletal muscle) were profiled by NMR and GC-MS, which helped ascertain optimal sampling times for different target tissues. We found that the time for overall optimal (13)C incorporation into tissue was 15-20 min but with substantial differences in (13)C labeling patterns of various organs that reflected their specific metabolism. Using this stable isotope resolved metabolomics (SIRM) approach, we have compared the (13)C metabolite profile of the lungs in the same mouse with or without an orthotopic lung tumor xenograft established from human PC14PE6 lung adenocarcinoma cells. The (13)C metabolite profile shows considerable differences in [U-(13)C]-glucose transformations between the two lung tissues, demonstrating the feasibility of applying SIRM to investigate metabolic networks of human cancer xenograft in the mouse model.

Identifiers

PMID21666826
PMCPMC3109995

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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.