Evidence map›Paper›PMID 20671121›Full record

ArticleBlood2010

Targeting of survivin by nanoliposomal ceramide induces complete remission in a rat model of NK-LGL leukemia.

Xin Liu, Lindsay Ryland, Jun Yang, Aijun Liao, Cesar Aliaga, Rebecca Watts, Su-Fern Tan, James Kaiser, Sriram S Shanmugavelandy, Andrew Rogers and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

54 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. The Role of Ceramide and Sphingolipid Metabolism in Cancer Therapeutics.Journal of oncology research and therapy · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Ceramide nanoliposomes augment the efficacy of venetoclax and cytarabine in models of acute myeloid leukemia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  10. Review
  11. Review
  12. Nanoliposome C6-Ceramide in combination with anti-CTLA4 antibody improves anti-tumor immunity in hepatocellular cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  13. Large granular lymphocytic leukemia: a brief review.American journal of blood research · 2022
    Review
  14. Targeting Sphingolipids for Cancer Therapy.Frontiers in oncology · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Sphingolipid metabolism and drug resistance in ovarian cancer.Cancer drug resistance (Alhambra, Calif.) · 2018
    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

22 authors at 4 institutions in 2 countries.

Xin LiuPenn State Hershey Cancer Institute, Pennsylvania State University College of Medicine, Hershey, PA, USA. Xliu2@hmc.psu.edu
Lindsay Ryland
Jun Yang
Aijun Liao
Cesar Aliaga
Rebecca Watts
Su-Fern Tan
James Kaiser
Sriram S Shanmugavelandy
Andrew Rogers
Kathleen Loughran
Bailey Petersen
Jonathan Yuen
Fanxue Meng
Kendall Thomas Baab
Nancy Ruth Jarbadan
Kathleen Broeg
Ranran Zhang
Jason Liao
Thomas Joseph Sayers
Mark Kester
Thomas P Loughran
Penn State Milton S. Hershey Medical Center · USPennsylvania State University · USChina Medical University · CNNational Cancer Institute · US

Funding

Promoting tumor cell apoptosis by death ligandsZIABC011056 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SAYERS, THOMAS · 2009 to 2018
$4.4M
Survival Mechanisms in Leukemic NK CellsR01CA098472 · NCI · UNIVERSITY OF VIRGINIA · PI LOUGHRAN, THOMAS P. · 2003 to 2016
$4.0M
Targeted Therapeutics of LGL Leukemia utilizing Ceramide NanoliposomesR01CA133525 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI LOUGHRAN, THOMAS P. · 2008 to 2012
$1.6M
NCI NIH HHS CA098472NCI NIH HHS CA133525NCI NIH HHS N01 CO012400NCI NIH HHS R01 CA098472NCI NIH HHS R01 CA133525
6 · The paper itself

Abstract

The natural killer (NK) type of aggressive large granular lymphocytic (LGL) leukemia is a fatal illness that pursues a rapid clinical course. There are no effective therapies for this illness, and pathogenetic mechanisms remain undefined. Here we report that the survivin was highly expressed in both aggressive and chronic leukemic NK cells but not in normal NK cells. In vitro treatment of human and rat NK-LGL leukemia cells with cell-permeable, short-chain C₆-ceramide (C₆) in nanoliposomal formulation led to caspase-dependent apoptosis and diminished survivin protein expression, in a time- and dose-dependent manner. Importantly, systemic intravenous delivery of nanoliposomal ceramide induced complete remission in the syngeneic Fischer F344 rat model of aggressive NK-LGL leukemia. Therapeutic efficacy was associated with decreased expression of survivin in vivo. These data suggest that in vivo targeting of survivin through delivery of nanoliposomal C₆-ceramide may be a promising therapeutic approach for a fatal leukemia.

Indexed as

AnimalsApoptosisCaspasesCell SurvivalCeramidesDisease Models, AnimalDown-RegulationExtracellular Signal-Regulated MAP KinasesHumansLeukemia, Large Granular LymphocyticLeukocytes, MononuclearLiposomesMicrotubule-Associated ProteinsMitochondriaNanoparticlesRatsBirc5 protein, ratCaspasesCeramidesExtracellular Signal-Regulated MAP KinasesLiposomesMicrotubule-Associated ProteinsSurvivin

Identifiers

PMID20671121
PMCPMC2993625
OpenAlexW2082046754

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.