Evidence map›Paper›PMID 26162894›Full record

ArticleLipids in health and disease2015

Saturated and mono-unsaturated lysophosphatidylcholine metabolism in tumour cells: a potential therapeutic target for preventing metastases.

Anna Raynor, Peter Jantscheff, Thomas Ross, Martin Schlesinger, Maurice Wilde, Sina Haasis, Tim Dreckmann, Gerd Bendas, Ulrich Massing

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

39 citing papers in PubMed, 72 citations in OpenAlex.

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  14. Characterization of Lipid Alterations by OncogenicOmics : a journal of integrative biology · 2023
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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

9 authors at 4 institutions in 3 countries.

Anna RaynorDepartment of Lipids & Liposomes, Tumor Biology Center, Clinical Research, Breisacher Str. 117, 79106, Freiburg, Germany. raynor@tumorbio.uni-freiburg.de.
Peter JantscheffProQinase GmbH, Breisacher Str. 117, 79106, Freiburg, Germany. p.jantscheff@proqinase.com.
Thomas RossDepartment of Pharmaceutical Chemistry, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany. tross@uni-bonn.de.
Martin SchlesingerDepartment of Pharmaceutical Chemistry, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany. martin.schlesinger@uni-bonn.de.
Maurice WildeDepartment of Lipids & Liposomes, Tumor Biology Center, Clinical Research, Breisacher Str. 117, 79106, Freiburg, Germany. maurice.wilde@web.de.
Sina HaasisDepartment of Lipids & Liposomes, Tumor Biology Center, Clinical Research, Breisacher Str. 117, 79106, Freiburg, Germany. sina.haasis@online.de.
Tim DreckmannDepartment of Lipids & Liposomes, Tumor Biology Center, Clinical Research, Breisacher Str. 117, 79106, Freiburg, Germany. timdreckmann@gmail.com.
Gerd BendasDepartment of Pharmaceutical Chemistry, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany. gbendas@uni-bonn.de.
Ulrich MassingDepartment of Lipids & Liposomes, Tumor Biology Center, Clinical Research, Breisacher Str. 117, 79106, Freiburg, Germany. ulrich.massing@pharmazie.uni-freiburg.de.
University of Freiburg · DEUniversity of Bonn · DECentre for Research and Development in Telecommunications (Brazil) · BRUniversity Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastasis is the leading cause of mortality in malignant diseases. Patients with metastasis often show reduced Lysophosphatidylcholine (LysoPC) plasma levels and treatment of metastatic tumour cells with saturated LysoPC species reduced their metastatic potential in vivo in mouse experiments. To provide a first insight into the interplay of tumour cells and LysoPC, the interactions of ten solid epithelial tumour cell lines and six leukaemic cell lines with saturated and mono-unsaturated LysoPC species were explored.

methodsLysoPC metabolism by the different tumour cells was investigated by a combination of cell culture assays, GC and MS techniques. Functional consequences of changed membrane properties were followed microscopically by detecting lateral lipid diffusion or cellular migration. Experimental metastasis studies in mice were performed after pretreatment of B16.F10 melanoma cells with LysoPC and FFA, respectively.

resultsIn contrast to the leukaemic cells, all solid tumour cells show a very fast extracellular degradation of the LysoPC species to free fatty acids (FFA) and glycerophosphocholine. We provide evidence that the formerly LysoPC bound FFA were rapidly incorporated into the cellular phospholipids, thereby changing the FA-compositions accordingly. A massive increase of the neutral lipid amount was observed, inducing the formation of lipid droplets. Saturated LysoPC and to a lesser extent also mono-unsaturated LysoPC increased the cell membrane rigidity, which is assumed to alter cellular functions involved in metastasis. According to that, saturated and mono-unsaturated LysoPC as well as the respective FFA reduced the metastatic potential of B16.F10 cells in mice. Application of high doses of liposomes mainly consisting of saturated PC was shown to be a suitable way to strongly increase the plasma level of saturated LysoPC in mice.

conclusionThese data show that solid tumours display a high activity to hydrolyse LysoPC followed by a very rapid uptake of the resulting FFA; a mechanistic model is provided. In contrast to the physiological mix of LysoPC species, saturated and mono-unsaturated LysoPC alone apparently attenuate the metastatic activity of tumours and the artificial increase of saturated and mono-unsaturated LysoPC in plasma appears as novel therapeutic approach to interfere with metastasis.

Indexed as

Molecular Targeted TherapyAnimalsCell Line, TumorCell MovementChemical FractionationFatty AcidsFatty Acids, UnsaturatedHumansLipid DropletsLysophosphatidylcholinesMaleMembrane FluidityMice, Inbred C57BLModels, BiologicalNeoplasm MetastasisNeoplasmsFatty AcidsFatty Acids, UnsaturatedLysophosphatidylcholines

Identifiers

PMID26162894
PMCPMC4499168
OpenAlexW1840616905

What OpenQuestion holds

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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.