Evidence map›Paper›PMID 24764256›Full record

ArticleNMR in biomedicine2014

Silencing of the glycerophosphocholine phosphodiesterase GDPD5 alters the phospholipid metabolite profile in a breast cancer model in vivo as monitored by (31) P MRS.

J P Wijnen, L Jiang, T R Greenwood, M Cheng, M Döpkens, M D Cao, Z M Bhujwalla, B Krishnamachary, D W J Klomp, K Glunde

Open access · greenAbstract read
In one paragraph

Article in NMR in biomedicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. DRUM: Inference of Disease-Associated mFrontiers in genetics · 2019
    Article
  7. Magnetic Resonance Spectroscopy Studies of Mouse Models of Cancer.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Choline metabolism-based molecular diagnosis of cancer: an update.Expert review of molecular diagnostics · 2015
    Review
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 3 countries.

J P WijnenThe Johns Hopkins University In vivo Cellular and Molecular Imaging Center, Division of Cancer Imaging Research, Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Radiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
L Jiang
T R Greenwood
M Cheng
M Döpkens
M D Cao
Z M Bhujwalla
B Krishnamachary
D W J Klomp
K Glunde
Imaging Center · USJohns Hopkins University · USJohns Hopkins Medicine · USNorwegian University of Science and Technology · NOUniversity Medical Center Utrecht · NL

Funding

Molecular studies of the MR-detectable oncometabolite glycerophosphocholineR01CA213428 · NCI · JOHNS HOPKINS UNIVERSITY · PI GLUNDE, KRISTINE · 2017 to 2021
$1.9M
Imaging hypoxia-driven signaling pathways in the breast tumor microenvironmentR01CA134695 · NCI · JOHNS HOPKINS UNIVERSITY · PI GLUNDE, KRISTINE · 2008 to 2012
$1.5M
NCI NIH HHS R01 CA134695NCI NIH HHS R01CA134695NCI NIH HHS R01 CA213428
6 · The paper itself

Abstract

Abnormal choline phospholipid metabolism is an emerging hallmark of cancer, which is implicated in carcinogenesis and tumor progression. The malignant metabolic phenotype is characterized by high levels of phosphocholine (PC) and relatively low levels of glycerophosphocholine (GPC) in aggressive breast cancer cells. Phosphorus ((31) P) MRS is able to non-invasively detect these water-soluble metabolites of choline as well as ethanolamine phospholipid metabolism. Here we have investigated the effects of stably silencing glycerophosphoester diesterase domain containing 5 (GDPD5), which is an enzyme with glycerophosphocholine phosphodiesterase activity, in MDA-MB-231 breast cancer cells and orthotopic tumor xenografts. Tumors in which GDPD5 was stably silenced with GDPD5-specific shRNA contained increased levels of GPC and phosphoethanolamine (PE) compared with control tumors.

Indexed as

Phosphorus IsotopesAnimalsBreast NeoplasmsCell Line, TumorFemaleHumansMagnetic Resonance SpectroscopyMicePhospholipidsPhosphoric Diester Hydrolasesglycerophosphocholine phosphodiesterasePhospholipidsPhosphoric Diester HydrolasesPhosphorus Isotopes31P MRSbreast cancerGDPD5glycerophosphoesterdiesterasein vivometabolismsilencing

Identifiers

PMID24764256
PMCPMC4162314
OpenAlexW1482605914

What Socratic 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 Socratic graph.