Evidence map›Paper›PMID 26807644›Full record

ReviewOncogenesis2016

Lipid metabolic reprogramming in cancer cells.

S Beloribi-Djefaflia, S Vasseur, F Guillaumond

Open access · goldAbstract readReview
In one paragraph

Review in Oncogenesis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 789 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
789citing papers in PubMed, 2 pooled it
58.7field-weighted citation impact, top 1% 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

789 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,378 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. NADPharmaceutical science advances · 2026
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  19. Proteome of CD9Life (Basel, Switzerland) · 2026
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729 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 1 country.

S Beloribi-DjefafliaINSERM, U1068, Centre de Recherche en Cancérologie de Marseille, Marseille, France.
S VasseurINSERM, U1068, Centre de Recherche en Cancérologie de Marseille, Marseille, France.
F GuillaumondINSERM, U1068, Centre de Recherche en Cancérologie de Marseille, Marseille, France.
Aix-Marseille Université · FRInserm · FRInstitut Paoli-Calmettes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many human diseases, including metabolic, immune and central nervous system disorders, as well as cancer, are the consequence of an alteration in lipid metabolic enzymes and their pathways. This illustrates the fundamental role played by lipids in maintaining membrane homeostasis and normal function in healthy cells. We reviewed the major lipid dysfunctions occurring during tumor development, as determined using systems biology approaches. In it, we provide detailed insight into the essential roles exerted by specific lipids in mediating intracellular oncogenic signaling, endoplasmic reticulum stress and bidirectional crosstalk between cells of the tumor microenvironment and cancer cells. Finally, we summarize the advances in ongoing research aimed at exploiting the dependency of cancer cells on lipids to abolish tumor progression.

Identifiers

PMID26807644
PMCPMC4728678
OpenAlexW2265836483

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.