Evidence map›Paper›PMID 27702801›Full record

ArticleBlood2016

LXR agonist treatment of blastic plasmacytoid dendritic cell neoplasm restores cholesterol efflux and triggers apoptosis.

Adam Ceroi, David Masson, Anne Roggy, Christophe Roumier, Cécile Chagué, Thierry Gauthier, Laure Philippe, Baptiste Lamarthée, Fanny Angelot-Delettre, Francis Bonnefoy and 7 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.5field-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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Exploring the nexus of nuclear receptors in hematological malignancies.Cellular and molecular life sciences : CMLS · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Lipid rafts as viral entry routes and immune platforms: A double-edged sword in SARS-CoV-2 infection?Biochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Review
  20. [Cholesterol Metabolism and Tumor Immunity].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022
    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

17 authors at 2 institutions in 1 country.

Adam CeroiUnité 1098, INSERM, Besançon, France.
David MassonLaboratoires d'Excellence (LabEx) Lipoprotéines et Santé: Prévention et Traitement des Maladies Inflammatoires et du Cancer (LipSTIC), Besançon/Dijon, France.
Anne RoggyUnité 1098, INSERM, Besançon, France.
Christophe RoumierLaboratoire d'Hématologie, Centre de Biologie Pathologie, Institut de Recherches sur le Cancer de Lille, Centre Hospitalier Régional Universitaire de Lille, INSERM Unité 837, Lille, France; and.
Cécile ChaguéUnité 1098, INSERM, Besançon, France.
Thierry GauthierUnité 1098, INSERM, Besançon, France.
Laure PhilippeUnité 1098, INSERM, Besançon, France.
Baptiste LamarthéeUnité 1098, INSERM, Besançon, France.
Fanny Angelot-DelettreUnité 1098, INSERM, Besançon, France.
Francis BonnefoyUnité 1098, INSERM, Besançon, France.
Sylvain PerrucheUnité 1098, INSERM, Besançon, France.
Sabeha BiichleUnité 1098, INSERM, Besançon, France.
Claude PreudhommeLaboratoire d'Hématologie, Centre de Biologie Pathologie, Institut de Recherches sur le Cancer de Lille, Centre Hospitalier Régional Universitaire de Lille, INSERM Unité 837, Lille, France; and.
Elisabeth MacintyreLaboratoire d'Onco-Hématologie, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Descartes, Université Sorbonne Paris Cité, INSERM Unité 1151, Paris, France.
Laurent LagrostLaboratoires d'Excellence (LabEx) Lipoprotéines et Santé: Prévention et Traitement des Maladies Inflammatoires et du Cancer (LipSTIC), Besançon/Dijon, France.
Francine Garnache-OttouUnité 1098, INSERM, Besançon, France.
Philippe SaasUnité 1098, INSERM, Besançon, France.ORCID 0000-0002-8857-9939
Inserm · FRHôpital Necker-Enfants Malades · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blastic plasmacytoid dendritic cell (PDC) neoplasm (BPDCN) is an aggressive hematological malignancy with a poor prognosis that derives from PDCs. No consensus for optimal treatment modalities is available today and the full characterization of this leukemia is still emerging. We identified here a BPDCN-specific transcriptomic profile when compared with those of acute myeloid leukemia and T-acute lymphoblastic leukemia, as well as the transcriptomic signature of primary PDCs. This BPDCN gene signature identified a dysregulation of genes involved in cholesterol homeostasis, some of them being liver X receptor (LXR) target genes. LXR agonist treatment of primary BPDCN cells and BPDCN cell lines restored LXR target gene expression and increased cholesterol efflux via the upregulation of adenosine triphosphate-binding cassette (ABC) transporters, ABCA1 and ABCG1. LXR agonist treatment was responsible for limiting BPDCN cell proliferation and inducing intrinsic apoptotic cell death. LXR activation in BPDCN cells was shown to interfere with 3 signaling pathways associated with leukemic cell survival, namely: NF-κB activation, as well as Akt and STAT5 phosphorylation in response to the BPDCN growth/survival factor interleukin-3. These effects were increased by the stimulation of cholesterol efflux through a lipid acceptor, the apolipoprotein A1. In vivo experiments using a mouse model of BPDCN cell xenograft revealed a decrease of leukemic cell infiltration and BPDCN-induced cytopenia associated with increased survival after LXR agonist treatment. This demonstrates that cholesterol homeostasis is modified in BPDCN and can be normalized by treatment with LXR agonists which can be proposed as a new therapeutic approach.

Indexed as

AnimalsAntineoplastic AgentsApoptosisATP Binding Cassette Transporter 1ATP Binding Cassette Transporter, Subfamily G, Member 1Cell Line, TumorCell ProliferationCholesterolDendritic CellsFemaleHumansInterleukin-3Liver X ReceptorsMaleMicePrecursor T-Cell Lymphoblastic Leukemia-LymphomaABCA1 protein, humanABCG1 protein, humanAntineoplastic AgentsATP Binding Cassette Transporter 1ATP Binding Cassette Transporter, Subfamily G, Member 1CholesterolIL3 protein, humanInterleukin-3Liver X ReceptorsProto-Oncogene Proteins c-aktSTAT5 Transcription Factor

Identifiers

PMID27702801
PMCPMC5271175
OpenAlexW2559956261

What OpenQuestion holds

Textmetadata
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.