Evidence map›Paper›PMID 23823656›Full record

ArticleLeukemia2014

Induced differentiation of acute myeloid leukemia cells by activation of retinoid X and liver X receptors.

P V Sanchez, S T Glantz, S Scotland, M T Kasner, M Carroll

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2014. 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
1.5field-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, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Antileukaemic Cell Proliferation and Cytotoxic Activity of Edible Golden Cordyceps (Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Effects of LG268 on Cell Proliferation and Apoptosis of NB4 Cells.International journal of medical sciences · 2016
    Article
  18. Targeting truncated RXRα for cancer therapy.Acta biochimica et biophysica Sinica · 2016
    Review
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

P V SanchezDivision of Hematology and Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA, USA.
S T GlantzDivision of Hematology and Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA, USA.
S ScotlandDivision of Hematology and Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA, USA.
M T KasnerKimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
M CarrollDivision of Hematology and Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA, USA.
University of Pennsylvania · USSidney Kimmel Cancer Center · US

Funding

Stem Cells, Differentiation and Therapeutic Resistance in AMLR01CA149566 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CARROLL, MARTIN · 2011 to 2015
$3.0M
Bexarotene Induction of Differentiation in AMLK01CA129151 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SANCHEZ, PATRICIA VANESSA · 2009 to 2013
$704k
NCI NIH HHS 1R01CA149566NCI NIH HHS K01 CA129151NCI NIH HHS K01-CA-129151NCI NIH HHS R01 CA149566
6 · The paper itself

Abstract

Use of all-trans retinoic acid (ATRA) as a differentiation agent has been limited to acute promyelocytic leukemia (APL) as non-APL leukemias are insensitive to ATRA. We recently demonstrated that the rexinoid, bexarotene, induces differentiation and therapeutic responses in patients with refractory AML. Rexinoids bind and activate retinoid X receptors (RXRs); however, rexinoids alone are incapable of activating retinoic acid receptor (RAR)/RXR complexes, suggesting that myeloid differentiation can occur independent of RAR. In this study, we demonstrate that rexinoid differentiation of AML cells is RAR independent and requires the expression of PU.1. Because of the promiscuousness of RXR with other nuclear receptors, myeloid differentiation by bexarotene with other nuclear receptor ligands was explored. Bexarotene cooperated with ATRA to enhance differentiation in some AML cell lines; however, the combination of bexarotene with the PPARγ agonist rosiglitazone did not. In contrast, bexarotene combined with liver X receptor (LXR) agonists, T0901317 or GW3965, induced potent differentiation and cytotoxicity in AML cell lines and primary human AML cells, but not in normal progenitor cells. These results suggest that RXR/LXR-regulated gene expression in normal cells is deregulated in AML cells and identifies a potential role for these agonists in differentiation therapy of non-APLs.

Indexed as

BenzenesulfonamidesBexaroteneCCAAT-Enhancer-Binding Protein-alphaCCAAT-Enhancer-Binding ProteinsCell DifferentiationCell Line, TumorFluorocarbonsHumansHydrocarbons, FluorinatedLeukemia, Myeloid, AcuteLiver X ReceptorsNicotinic AcidsOrphan Nuclear ReceptorsProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Retinoid X ReceptorsBenzenesulfonamidesBexaroteneCCAAT-Enhancer-Binding Protein-alphaCCAAT-Enhancer-Binding ProteinsCEBPE protein, humanFluorocarbonsHydrocarbons, FluorinatedLG 100268Liver X ReceptorsNicotinic AcidsOrphan Nuclear ReceptorsProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Retinoid X ReceptorsSulfonamidesT0901317TetrahydronaphthalenesTrans-ActivatorsTretinoin

Identifiers

PMID23823656
PMCPMC8835482
OpenAlexW2037352728

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.