Evidence map›Paper›PMID 36106439›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2022

Ceramide nanoliposomes augment the efficacy of venetoclax and cytarabine in models of acute myeloid leukemia.

Andrei V Khokhlatchev, Arati Sharma, Tye G Deering, Jeremy J P Shaw, Pedro Costa-Pinheiro, Upendarrao Golla, Charyguly Annageldiyev, Myles C Cabot, Mark R Conaway, Su-Fern Tan and 6 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Therapeutic Potential of Ceramide in Cancer Treatment.Journal of cancer research and oncobiology · 2024
    Article
  6. Article
  7. The Role of Ceramide and Sphingolipid Metabolism in Cancer Therapeutics.Journal of oncology research and therapy · 2024
    Article
  8. Influences on the Hematopoietic Stem Cell Niche.SciBase hematology & blood disorders · 2024
    Article
  9. Article
  10. Review
  11. Review
  12. 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
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

16 authors at 4 institutions in 1 country.

Andrei V KhokhlatchevDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia, USA.
Arati SharmaDivision of Hematology and Oncology, Department of Medicine, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Tye G DeeringDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia, USA.
Jeremy J P ShawDepartment of Experimental Pathology, University of Virginia, Charlottesville, Virginia, USA.
Pedro Costa-PinheiroDepartment of Experimental Pathology, University of Virginia, Charlottesville, Virginia, USA.
Upendarrao GollaDivision of Hematology and Oncology, Department of Medicine, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Charyguly AnnageldiyevDivision of Hematology and Oncology, Department of Medicine, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Myles C CabotDepartment of Biochemistry and Molecular Biology, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA.
Mark R ConawayUniversity of Virginia School of Medicine, Public Health Sciences, Charlottesville, Virginia, USA.
Su-Fern TanDivision of Hematology and Oncology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Johnson UngDivision of Hematology and Oncology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
David J FeithDivision of Hematology and Oncology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Thomas P LoughranDivision of Hematology and Oncology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
David F ClaxtonDivision of Hematology and Oncology, Department of Medicine, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Todd E FoxDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0000-0001-5170-3951
Mark KesterDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia, USA.
University of Virginia · USPennsylvania State University · USUniversity of Virginia Cancer CenterEast Carolina University · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Dina Gould Halme · 1987 to 2026
$72.1M
Tissue Repository and Animal Models CoreP01CA171983 · NCI · UNIVERSITY OF VIRGINIA · PI JANES, KEVIN A · 2013 to 2024
$19.9M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
Ceramide NanoLiposomes as a novel therapeutic for prostate cancerK00CA245802 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DA COSTA PINHEIRO, PEDRO FILIPE · 2021 to 2024
$313k
Ceramide NanoLiposomes as a novel therapeutic for prostate cancerF99CA245802 · NCI · UNIVERSITY OF VIRGINIA · PI DA COSTA PINHEIRO, PEDRO FILIPE · 2019 to 2020
$69k
Targeting Acid Ceramidase and Bcl-2 in Acute Myeloid LeukemiaF31CA271809 · NCI · UNIVERSITY OF VIRGINIA · PI UNG, JOHNSON · 2022 to 2023
$46k
NCI NIH HHS F31 CA271809NCI NIH HHS F99 CA245802NCI NIH HHS K00 CA245802NCI NIH HHS P01 CA171983NCI NIH HHS P30 CA044579NCI NIH HHS T32 CA009109
6 · The paper itself

Abstract

Despite several new therapeutic options for acute myeloid leukemia (AML), disease relapse remains a significant challenge. We have previously demonstrated that augmenting ceramides can counter various drug-resistance mechanisms, leading to enhanced cell death in cancer cells and extended survival in animal models. Using a nanoscale delivery system for ceramide (ceramide nanoliposomes, CNL), we investigated the effect of CNL within a standard of care venetoclax/cytarabine (Ara-C) regimen. We demonstrate that CNL augmented the efficacy of venetoclax/cytarabine in in vitro, ex vivo, and in vivo models of AML. CNL treatment induced non-apoptotic cytotoxicity, and augmented cell death induced by Ara-C and venetoclax. Mechanistically, CNL reduced both venetoclax (Mcl-1) and cytarabine (Chk1) drug-resistant signaling pathways. Moreover, venetoclax and Ara-C augmented the generation of endogenous pro-death ceramide species, which was intensified with CNL. Taken together, CNL has the potential to be utilized as an adjuvant therapy to improve outcomes, potentially extending survival, in patients with AML.

Indexed as

Antineoplastic AgentsLeukemia, Myeloid, AcuteAnimalsBridged Bicyclo Compounds, HeterocyclicCeramidesCytarabineSulfonamidesAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicCeramidesCytarabineSulfonamidesvenetoclaxcell deathceramidescytarabinedrug resistanceleukemia, myeloid, acutemodels, animalrecurrencesignal transductionstandard of carevenetoclax

Identifiers

PMID36106439
PMCPMC9544744
OpenAlexW4295899286

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.