Evidence map›Paper›PMID 29784041›Full record

ReviewCancer communications (London, England)2018

Lipid metabolism reprogramming and its potential targets in cancer.

Chunming Cheng, Feng Geng, Xiang Cheng, Deliang Guo

Open access · goldAbstract readReview
In one paragraph

Review in Cancer communications (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 538 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
538citing papers in PubMed, 1 pooled it
14.9field-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

538 citing papers in PubMed, 1 synthesis or guideline pooled it, 810 citations in OpenAlex.

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  12. Anoikis in cancer: molecular mechanisms, resistance, and therapeutic strategies.Apoptosis : an international journal on programmed cell death · 2026
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478 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

4 authors at 1 institution in 1 country.

Chunming ChengDepartment of Radiation Oncology, The Ohio State University James Comprehensive Cancer Center and College of Medicine, Columbus, OH, 43210, USA.
Feng GengDepartment of Radiation Oncology, The Ohio State University James Comprehensive Cancer Center and College of Medicine, Columbus, OH, 43210, USA.
Xiang ChengDepartment of Radiation Oncology, The Ohio State University James Comprehensive Cancer Center and College of Medicine, Columbus, OH, 43210, USA.
Deliang GuoDepartment of Radiation Oncology, The Ohio State University James Comprehensive Cancer Center and College of Medicine, Columbus, OH, 43210, USA. deliang.guo@osumc.edu.
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

Determining the role of lipid droplets in glioblastoma and their therapeutic potentialR01NS104332 · NINDS · OHIO STATE UNIVERSITY · PI Deliang Guo · 2018 to 2026
$4.2M
Targeting the cholesterol metabolism to treat glioblastomaR01NS079701 · NINDS · OHIO STATE UNIVERSITY · PI GUO, DELIANG · 2013 to 2017
$1.7M
American Cancer Society RSG-14-228-01-CSMNIH HHS NS079701NINDS NIH HHS R01 NS079701NINDS NIH HHS R01 NS104332
6 · The paper itself

Abstract

Reprogramming of lipid metabolism is a newly recognized hallmark of malignancy. Increased lipid uptake, storage and lipogenesis occur in a variety of cancers and contribute to rapid tumor growth. Lipids constitute the basic structure of membranes and also function as signaling molecules and energy sources. Sterol regulatory element-binding proteins (SREBPs), a family of membrane-bound transcription factors in the endoplasmic reticulum, play a central role in the regulation of lipid metabolism. Recent studies have revealed that SREBPs are highly up-regulated in various cancers and promote tumor growth. SREBP cleavage-activating protein is a key transporter in the trafficking and activation of SREBPs as well as a critical glucose sensor, thus linking glucose metabolism and de novo lipid synthesis. Targeting altered lipid metabolic pathways has become a promising anti-cancer strategy. This review summarizes recent progress in our understanding of lipid metabolism regulation in malignancy, and highlights potential molecular targets and their inhibitors for cancer treatment.

Indexed as

AnimalsAntineoplastic AgentsEndoplasmic ReticulumHumansIntracellular Signaling Peptides and ProteinsLipid MetabolismLipogenesisMembrane ProteinsModels, BiologicalNeoplasmsSterol Regulatory Element Binding ProteinsAntineoplastic AgentsIntracellular Signaling Peptides and ProteinsMembrane ProteinsSREBP cleavage-activating proteinSterol Regulatory Element Binding ProteinsCancerCholesterolFatty acidsLipid dropletsLipid metabolismSCAPSREBPs

Identifiers

PMID29784041
PMCPMC5993136
OpenAlexW2805393256

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.