Evidence map›Paper›PMID 24872387›Full record

ArticleCancer research2014

Selenium suppresses leukemia through the action of endogenous eicosanoids.

Ujjawal H Gandhi, Naveen Kaushal, Shailaja Hegde, Emily R Finch, Avinash K Kudva, Mary J Kennett, Craig T Jordan, Robert F Paulson, K Sandeep Prabhu

Abstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Therapeutic Benefits of Selenium in Hematological Malignancies.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Review
  8. Selenium and selenoproteins in prostanoid metabolism and immunity.Critical reviews in biochemistry and molecular biology · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Redox Regulation in Cancer Stem Cells.Oxidative medicine and cellular longevity · 2015
    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

9 authors at 2 institutions in 1 country.

Ujjawal H GandhiAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and.
Naveen KaushalAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and.
Shailaja HegdeAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and.
Emily R FinchAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and.
Avinash K KudvaAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and.
Mary J KennettAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and.
Craig T JordanDivision of Hematology, Hematologic Malignancies, and Stem Cell Transplantation, University of Colorado, Anshutz Medical Campus, Aurora, Colorado.
Robert F PaulsonAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and ksp4@psu.edu rfp5@psu.edu.
K Sandeep PrabhuAuthors' Affiliations: Department of Veterinary and Biomedical Sciences, Center for Molecular Immunology and Infectious Disease and Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania; and ksp4@psu.edu rfp5@psu.edu.
Pennsylvania State University · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Integration of Palliative Care for Cancer Patients on Phase I TrialsR01CA177562 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI FERRELL, BETTY R · 2014 to 2018
$6.8M
Training Program in Cancer TherapeuticsT32CA117846 · NCI · UNIVERSITY OF CINCINNATI · PI PRICE, CAROLYN M, TAKIAR, VINITA · 2006 to 2022
$6.5M
The BMP4 dependent stress erythropoiesis pathway in short-term radioprotectionR01DK080040 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PAULSON, ROBERT FRANK · 2009 to 2017
$2.6M
Cellular Selenium Status and PGJ2 Metabolism (PA-17-078 supplement 2017)R01DK077152 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PRABHU, KUMBLE SANDEEP · 2008 to 2018
$2.5M
Targeting Leukemia Stem Cells with Dietary SeleniumR01CA162665 · NCI · PENNSYLVANIA STATE UNIVERSITY, THE · PI PRABHU, KUMBLE SANDEEP · 2012 to 2016
$1.5M
Cellular selenium and PGJ2 metabolismR56DK077152 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PRABHU, KUMBLE SANDEEP · 2021 to 2021
$386k
BMP4 dependent stress erythropoiesis pathway in short-term radioprotectionR56DK080040 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PAULSON, ROBERT FRANK · 2013 to 2013
$75k
NCI NIH HHS CA162665NCI NIH HHS R01 CA162665NCI NIH HHS R01 CA177562NCI NIH HHS T32 CA117846NIDDK NIH HHS DK077152NIDDK NIH HHS DK 080040NIDDK NIH HHS R01 DK077152NIDDK NIH HHS R01 DK080040NIDDK NIH HHS R56 DK077152NIDDK NIH HHS R56 DK080040
6 · The paper itself

Abstract

Eradicating cancer stem-like cells (CSC) may be essential to fully eradicate cancer. Metabolic changes in CSC could hold a key to their targeting. Here, we report that the dietary micronutrient selenium can trigger apoptosis of CSC derived from chronic or acute myelogenous leukemias when administered at supraphysiologic but nontoxic doses. In leukemia CSC, selenium treatment activated ATM-p53-dependent apoptosis accompanied by increased intracellular levels of reactive oxygen species. Importantly, the same treatment did not trigger apoptosis in hematopoietic stem cells. Serial transplantation studies with BCR-ABL-expressing CSC revealed that the selenium status in mice was a key determinant of CSC survival. Selenium action relied upon the endogenous production of the cyclooxygenase-derived prostaglandins Δ(12)-PGJ2 and 15d-PGJ2. Accordingly, nonsteroidal anti-inflammatory drugs and NADPH oxidase inhibitors abrogated the ability of selenium to trigger apoptosis in leukemia CSC. Our results reveal how selenium-dependent modulation of arachidonic acid metabolism can be directed to trigger apoptosis of primary human and murine CSC in leukemia.

Indexed as

AnimalsApoptosisArachidonic AcidsCell Transformation, NeoplasticCytochrome P-450 Enzyme SystemEicosanoidsHumansLeukemiaMacrophagesMaleMiceNeoplastic Stem CellsOxidative StressReactive Oxygen SpeciesSeleniumSignal TransductionArachidonic AcidsCytochrome P-450 Enzyme SystemEicosanoidsReactive Oxygen SpeciesSeleniumTumor Suppressor Protein p53

Identifiers

PMID24872387
PMCPMC4102641
OpenAlexW2132244024

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.