Evidence map›Paper›PMID 21510650›Full record

ArticleJournal of proteome research2011

NMR-based metabolomic analysis of the molecular pathogenesis of therapy-related myelodysplasia/acute myeloid leukemia.

Kristin E Cano, Liang Li, Smita Bhatia, Ravi Bhatia, Stephen J Forman, Yuan Chen

Abstract read
In one paragraph

Article in Journal of proteome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  8. Article
  9. Pharmacometabolomics by NMR in Oncology: A Systematic Review.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  10. Article
  11. Metabolic Dysfunction and Asthma: Current Perspectives.Journal of asthma and allergy · 2020
    Review
  12. High-Throughput Metabolomics by 1D NMR.Angewandte Chemie (International ed. in English) · 2019
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
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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 2 institutions in 1 country.

Kristin E CanoDepartment of Molecular Medicine, Beckman Research Institute of the City of Hope, Duarte, California 91010, USA.
Liang Li
Smita Bhatia
Ravi Bhatia
Stephen J Forman
Yuan Chen
Beckman Research InstituteCity of Hope · US

Funding

ZOPOLRESTAT IN NORMOTENSIVE, TYPE 1 DIA WITH INCIPIENT NEPHROPATHYM01RR000043 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZAIA, JOHN A · 1985 to 2010
$76.4M
Transplant for Lymphoma:Therapy-Related LeukemiaP50CA107399 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI FORMAN, STEPHEN J, KWAK, LARRY W · 2004 to 2022
$35.5M
SUMO modification and DNA damage response in cancer therapyR01GM086171 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, YUAN · 2008 to 2020
$5.2M
Abnormalities in gene expression in therapy-related MDSR01HL083050 · NHLBI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI BHATIA, RAVI · 2005 to 2008
$2.3M
The Enzymatic Pathway of a Ubiquitin-Like ModificationR01GM074748 · NIGMS · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI CHEN, YUAN · 2007 to 2010
$1.5M
NCI NIH HHS P50 CA107399NCRR NIH HHS 5M01 RR00043NCRR NIH HHS M01 RR000043NHLBI NIH HHS R01 HL083050NIGMS NIH HHS R01 GM074748NIGMS NIH HHS R01 GM086171PHS HHS R01 086171
6 · The paper itself

Abstract

Hematopoietic stem cell transplantation is the oldest and most successful form of stem cell therapy. High dose therapy (HDT) followed by hematopoietic stem cell transplantation allows physicians to administer increased amounts of chemotherapy and/or radiation while minimizing negative side effects such as damage to blood-producing bone marrow cells. Although HDT is successful in treating a wide range of cancers, it leads to lethal therapy-related myelodysplasia syndrome or acute myeloid leukemia (t-MDS/AML) in 5--10% of patients undergoing autologous hematopoietic cell transplantation for Hodgkin lymphoma and non-Hodgkin lymphoma. In this study, we carried out metabolomic analysis of peripheral blood stem cell samples collected in a cohort of patients before hematopoietic cell transplantation to gain insights into the molecular and cellular pathogenesis of t-MDS. Nonparametric tests and multivariate analyses were used to compare the metabolite concentrations in samples from patients that developed t-MDS within 5 years of transplantation and the patients that did not. The results suggest that the development of t-MDS is associated with dysfunctions in cellular metabolic pathways. The top canonical pathways suggested by the metabolomic analysis include alanine and aspartate metabolism, glyoxylate and dicarboxylate metabolism, phenylalanine metabolism, citrate acid cycle, and aminoacyl-t-RNA biosynthesis. Dysfunctions in these pathways indicate mitochondrial dysfunction that would result in decreased ability to detoxify reactive oxygen species generated by chemo and radiation therapy, therefore leading to cancer-causing mutations. These observations suggest predisposing factors for the development of t-MDS.

Indexed as

MetabolomeAdolescentAdultAdult Stem CellsAgedFemaleHematopoietic Stem Cell TransplantationHodgkin DiseaseHumansHydrophobic and Hydrophilic InteractionsLeukemia, Myeloid, AcuteLymphoma, Non-HodgkinMagnetic Resonance SpectroscopyMaleMetabolic Networks and PathwaysMiddle Aged

Identifiers

PMID21510650
PMCPMC3390255
OpenAlexW1968426302

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.