Evidence map›Paper›PMID 20305696›Full record

ArticleOncogene2010

Ganglioside synthase knockout in oncogene-transformed fibroblasts depletes gangliosides and impairs tumor growth.

Y Liu, S Yan, A Wondimu, D Bob, M Weiss, K Sliwinski, J Villar, V Notario, M Sutherland, A M Colberg-Poley and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Gangliosides and Neuroblastomas.International journal of molecular sciences · 2020
    Review
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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

11 authors at 2 institutions in 1 country.

Y LiuCenter for Cancer and Immunology Research, Children's National Medical Center, NW, Washington, DC 20010, USA.
S Yan
A Wondimu
D Bob
M Weiss
K Sliwinski
J Villar
V Notario
M Sutherland
A M Colberg-Poley
S Ladisch
Children's National · USGeorgetown University · US

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SASISEKHARAN, RAM · 2001 to 2010
$80.3M
Role of gangliosides in tumor progressionR01CA061010 · NCI · CHILDREN'S RESEARCH INSTITUTE · PI LADISCH, STEPHAN · 1993 to 2012
$4.0M
FUNCTION OF THE PCPH ONCOGENE IN MAMM;CARCINOGENESISR01CA064472 · NCI · GEORGETOWN UNIVERSITY · PI NOTARIO, VICENTE · 1995 to 2007
$2.0M
IMMUNOSUPPRESSIVE NEUROBLASTOMA TUMOR GANGLIOSIDESR01CA042361 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LADISCH, STEPHAN · 1986 to 2008
$1.6M
NCI NIH HHS CA42361NCI NIH HHS CA61010NCI NIH HHS CA64472NCI NIH HHS R01 CA042361NCI NIH HHS R01 CA061010NCI NIH HHS R01 CA064472NIGMS NIH HHS GM62116NIGMS NIH HHS U54 GM062116
6 · The paper itself

Abstract

Biologically active membrane gangliosides, expressed and released by many human tumors, are hypothesized to significantly impact tumor progression. Lack of a model of complete and specific tumor ganglioside depletion in vivo, however, has hampered elucidation of their role. Here, we report the creation of a novel, stable, genetically induced tumor cell system resulting in specific and complete blockade of ganglioside synthesis. Wild-type (WT) and GM3 synthase/GM2 synthase double knockout (DKO) murine embryonic fibroblasts were transformed using amphotropic retrovirus-transduced oncogenes (pBABE-c-Myc(T58A)+H-RasG12V). The transformed cells, WT(t) and DKO(t) respectively, evidenced comparable integrated copy numbers and oncogene expression. Ganglioside synthesis was completely blocked in the DKO(t) cells, importantly without triggering an alternate pathway of ganglioside synthesis. Ganglioside depletion (to <0.5 nmol/10(7) cells from 9 to 11 nmol/10(7) WT(t) or untransfected normal fibroblasts) did not adversely affect cell proliferation kinetics but did reduce cell migration on fibronectin-coated wells, consistent with our previous observations in ganglioside-depleted normal human fibroblasts. Strikingly, despite similar oncogene expression and growth kinetics, DKO(t) cells evidenced significantly impaired tumor growth in syngeneic immunocompetent mice, underscoring the pivotal role of tumor cell gangliosides and providing an ideal system for probing their mechanisms of action in vivo.

Indexed as

OncogenesAnimalsCell Growth ProcessesCell MovementCells, CulturedCell Transformation, NeoplasticFibroblastsGangliosidesGenes, mycGenes, rasHumansMiceMice, Inbred C57BLMice, KnockoutN-AcetylgalactosaminyltransferasesSialyltransferasesGangliosideshaematoside synthetaseN-Acetylgalactosaminyltransferases(N-acetylneuraminyl)-galactosylglucosylceramide N-acetylgalactosaminyltransferaseSialyltransferases

Identifiers

PMID20305696
PMCPMC2880627
OpenAlexW2002461944

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.