Evidence map›Paper›PMID 32518949›Full record

ArticleBlood2020

Developing new ceramide analogs and identifying novel sphingolipid-controlled genes against a virus-associated lymphoma.

Jungang Chen, Navneet Goyal, Lu Dai, Zhen Lin, Luis Del Valle, Jovanny Zabaleta, Jiawang Liu, Steven R Post, Maryam Foroozesh, Zhiqiang Qin

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2020. 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
0.4field-weighted citation impact, top 40% 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, 11 citations in OpenAlex.

  1. Article
  2. The Role of Ceramides in Metabolic and Cardiovascular Diseases.Journal of cardiovascular development and disease · 2026
    Review
  3. Article
  4. Article
  5. Therapeutic Potential of Ceramide in Cancer Treatment.Journal of cancer research and oncobiology · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

10 authors at 5 institutions in 1 country.

Jungang ChenDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Navneet GoyalDepartment of Chemistry, Xavier University of Louisiana, New Orleans, LA.
Lu DaiDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Zhen LinDepartment of Pathology, Tulane University Health Sciences Center, Tulane Cancer Center, New Orleans, LA.
Luis Del ValleDepartment of Pathology and.
Jovanny ZabaletaDepartment of Pediatrics, Louisiana State University Health Sciences Center, Louisiana Cancer Research Center, New Orleans, LA; and.
Jiawang LiuDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN.
Steven R PostDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Maryam ForoozeshDepartment of Chemistry, Xavier University of Louisiana, New Orleans, LA.
Zhiqiang QinDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Winthrop Rockefeller Foundation · USXavier University of Louisiana · USLouisiana State University · USTulane University · USUniversity of Tennessee Health Science Center · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Leigh Lamonica · 2012 to 2026
$69.1M
Translational Genomics Core (TGC)P20GM121288 · NIGMS · LSU HEALTH SCIENCES CENTER · PI Jennifer Erin Cameron · 2017 to 2026
$22.4M
Xavier's RCMI Cancer Research ProgramG12MD007595 · NIMHD · XAVIER UNIVERSITY OF LOUISIANA · PI D'AMOUR, GENE, WANG, GUANGDI · 2012 to 2018
$15.7M
Periodontal bacteria enhance oral KSHV pathogenesis and Kaposi’s Sarcoma development in HIV+ patientsR01CA228166 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI FORREST, JAMES CRAIG, POST, STEVEN · 2018 to 2023
$1.9M
Pilot ProjectP20CA202922 · NCI · LSU HEALTH SCIENCES CENTER · PI GREGORY, PAULA ELIZABETH, MIELE, LUCIO · 2017 to 2020
$987k
Multi-Target, Mechanism-Based Drug Design for the Treatment of Breast Cancer: SynR15CA159059 · NCI · XAVIER UNIVERSITY OF LOUISIANA · PI FOROOZESH, MARYAM · 2011 to 2011
$370k
NCI NIH HHS P20 CA202922NCI NIH HHS R01 CA228166NCI NIH HHS R15 CA159059NIGMS NIH HHS P20 GM121288NIGMS NIH HHS U54 GM104940NIMHD NIH HHS G12 MD007595
6 · The paper itself

Abstract

Primary effusion lymphoma (PEL) is an aggressive malignancy with poor prognosis even under chemotherapy. Kaposi sarcoma-associated herpesvirus (KSHV), one of the human oncogenic viruses, is the principal causative agent. Currently, there is no specific treatment for PEL; therefore, developing new therapies is of great importance. Sphingolipid metabolism plays an important role in determining the fate of tumor cells. Our previous studies have demonstrated that there is a correlation between sphingolipid metabolism and KSHV+ tumor cell survival. To further develop sphingolipid metabolism-targeted therapy, after screening a series of newly synthesized ceramide analogs, here, we have identified compounds with effective anti-PEL activity. These compounds induce significant PEL apoptosis, cell-cycle arrest, and intracellular ceramide production through regulation of ceramide synthesizing or ceramide metabolizing enzymes and dramatically suppress tumor progression without visible toxicity in vivo. These new compounds also increase viral lytic gene expression in PEL cells. Our comparative transcriptomic analysis revealed their mechanisms of action for inducing PEL cell death and identified a subset of novel cellular genes, including AURKA and CDCA3, controlled by sphingolipid metabolism, and required for PEL survival with functional validation. These data provide the framework for the development of promising sphingolipid-based therapies against this virus-associated malignancy.

Indexed as

AnimalsApoptosisAurora Kinase ACell Cycle ProteinsCell SurvivalCeramidesFemaleGene Expression ProfilingHerpesvirus 8, HumanHumansLymphoma, Primary EffusionMiceMice, Inbred NODMice, SCIDSarcoma, KaposiSphingolipidsAURKA protein, humanAurora Kinase ACDCA3 protein, humanCell Cycle ProteinsCeramidesSphingolipids

Identifiers

PMID32518949
PMCPMC7645984
OpenAlexW3033315127

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.