Evidence map›Paper›PMID 23671696›Full record

ArticlePloS one2013

Use of a glycolipid inhibitor to ameliorate renal cancer in a mouse model.

Subroto Chatterjee, Nezar Alsaeedi, Jennifer Hou, Veera Venkata Ratnam Bandaru, Lan Wu, Marc K Halushka, Roberto Pili, Georges Ndikuyeze, Norman J Haughey

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Central Roles of Glucosylceramide in Driving Cancer Pathogenesis.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Lipids as Targets for Renal Cell Carcinoma Therapy.International journal of molecular sciences · 2023
    Review
  7. Targeting the Sphingolipid Rheostat in Gliomas.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

9 authors at 2 institutions in 1 country.

Subroto ChatterjeeDepartment of Pediatrics, Division of Pediatric Cardiology, The Johns Hopkins Medical Institutions, Baltimore, Maryland, USA. schatte2@jhmi.edu
Nezar Alsaeedi
Jennifer Hou
Veera Venkata Ratnam Bandaru
Lan Wu
Marc K Halushka
Roberto Pili
Georges Ndikuyeze
Norman J Haughey
Johns Hopkins University · USRoswell Park Comprehensive Cancer Center · US

Funding

Therapeutic CoreP30MH075673 · NIMH · JOHNS HOPKINS UNIVERSITY · PI Leah Helane Rubin · 2006 to 2026
$33.2M
Shared Resource CoresP01HL107153 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HART, GERALD WARREN · 2011 to 2017
$16.8M
Research BaseP30DK090868 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WATNICK, TERRY J · 2010 to 2019
$11.1M
Mechanisms of Neuroinflammation in HANDR01MH077542 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HAUGHEY, NORMAN J · 2007 to 2016
$3.4M
HIV Associated CNS Dysfunction with AgingR01AG023471 · NIA · JOHNS HOPKINS UNIVERSITY · PI HAUGHEY, NORMAN J · 2003 to 2007
$1.8M
HIV Mediated Dysfunction of Neural Progenitor CellsR21MH072534 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HAUGHEY, NORMAN J · 2005 to 2006
$421k
NHLBI NIH HHS P01 HL107153NHLBI NIH HHS P0-1-HL-107153-01NIA NIH HHS R01 AG023471NIDDK NIH HHS P30 DK090868NIMH NIH HHS R01 MH077542NIMH NIH HHS R21 MH072534
6 · The paper itself

Abstract

In a xenograft model wherein, live renal cancer cells were implanted under the kidney capsule in mice, revealed a 30-fold increase in tumor volume over a period of 26 days and this was accompanied with a 32-fold increase in the level of lactosylceramide (LacCer). Mice fed D- threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), an inhibitor of glucosylceramide synthase and lactosylceramide synthase (LCS: β-1,4-GalT-V), showed marked reduction in tumor volume. This was accompanied by a decrease in the mass of lactosylceramide and an increase in glucosylceramide (GlcCer) level. Mechanistic studies revealed that D-PDMP inhibited cell proliferation and angiogenesis by inhibiting p44MAPK, p-AKT-1 pathway and mammalian target for rapamycin (mTOR). By linking glycosphingolipid synthesis with tumor growth, renal cancer progression and regression can be evaluated. Thus inhibiting glycosphingolipid synthesis can be a bonafide target to prevent the progression of other types of cancer.

Indexed as

Disease Models, AnimalAdministration, OralAnimalsAntigens, CDBlotting, WesternDisease ProgressionEnzyme InhibitorsGalactosyltransferasesGlucosylceramidesGlucosyltransferasesKidneyKidney NeoplasmsLactosylceramidesMiceMice, Inbred BALB CMorpholinesAntigens, CDCDw17 antigenceramide glucosyltransferaseEnzyme InhibitorsGalactosyltransferasesGlucosylceramidesGlucosyltransferasesLactosylceramidesMorpholinesPeptide FragmentsProto-Oncogene Proteins c-aktRV 538Transcription FactorsTumor Suppressor Protein p53UDPgalactose-glucosylceramide galactosyltransferaseWDR77 protein, mouse

Identifiers

PMID23671696
PMCPMC3650082
OpenAlexW2015249167

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.