Evidence map›Paper›PMID 23859617›Full record

ReviewCurrent pharmaceutical design2014

Targeting SREBP-1-driven lipid metabolism to treat cancer.

Deliang Guo, Erica Hlavin Bell, Paul Mischel, Arnab Chakravarti

Abstract readReview
In one paragraph

Review in Current pharmaceutical design, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 186 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
186citing papers in PubMed, 3 pooled it
6.0field-weighted citation impact, top 3% 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

186 citing papers in PubMed, 3 syntheses or guidelines pooled it, 311 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. [Molecular imaging and biology · 2017
    Trial
  5. Review
  6. Genomic alterations and their correlation with metabolic-related genes in lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Anti-Cancer Activity ofMarine drugs · 2025
    Article
  19. Article
  20. Review

126 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.

Deliang Guo
Erica Hlavin Bell
Paul Mischel
Arnab ChakravartiDepartment of Radiation Oncology, Ohio State University Comprehensive Cancer Center and Arthur G. James Cancer Hospital, 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

Targeting the cholesterol metabolism to treat glioblastomaR01NS079701 · NINDS · OHIO STATE UNIVERSITY · PI GUO, DELIANG · 2013 to 2017
$1.7M
Targeting SREBP-1 regulated fatty acid synthesis pathway to treat glioblastomaR21NS072838 · NINDS · OHIO STATE UNIVERSITY · PI GUO, DELIANG · 2011 to 2012
$419k
VOLTAGE-SENSITIVE ION CHANNELS IN GLIAL CELLSF32NS007970 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI BARRES, BEN A · 1986 to 1988
–
NINDS NIH HHS NS072838NINDS NIH HHS NS079701ANINDS NIH HHS R01 NS079701NINDS NIH HHS R21 NS072838
6 · The paper itself

Abstract

Metabolic reprogramming is a hallmark of cancer. Oncogenic growth signaling regulates glucose, glutamine and lipid metabolism to meet the bioenergetics and biosynthetic demands of rapidly proliferating tumor cells. Emerging evidence indicates that sterol regulatory element-binding protein 1 (SREBP-1), a master transcription factor that controls lipid metabolism, is a critical link between oncogenic signaling and tumor metabolism. We recently demonstrated that SREBP-1 is required for the survival of mutant EGFR-containing glioblastoma, and that this pro-survival metabolic pathway is mediated, in part, by SREBP-1-dependent upregulation of the fatty acid synthesis and low density lipoprotein (LDL) receptor (LDLR). These results have identified EGFR/PI3K/Akt/SREBP-1 signaling pathway that promotes growth and survival in glioblastoma, and potentially other cancer types. Here, we summarize recent insights in the understanding of cancer lipid metabolism, and discuss the evidence linking SREBP-1 with PI3K/Akt signaling-controlled glycolysis and with Myc-regulated glutaminolysis to lipid metabolism. We also discuss the development of potential drugs targeting the SREBP-1- driven lipid metabolism as anti-cancer agents.

Indexed as

AnimalsCholesterolGlutamic AcidGlycolysisHumansLipid MetabolismLipogenesisNeoplasmsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, LDLSterol Regulatory Element Binding Protein 1CholesterolGlutamic AcidPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, LDLSterol Regulatory Element Binding Protein 1

Identifiers

PMID23859617
PMCPMC4148912
OpenAlexW2171640413

What OpenQuestion holds

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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.