Evidence map›Paper›PMID 27973397›Full record

ReviewInternational journal of molecular sciences2016

p53 as a Regulator of Lipid Metabolism in Cancer.

Alejandro Parrales, Tomoo Iwakuma

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

62 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. [p53-SOAT1 Axis: A Novel Target for Tumor Lipid Metabolism and Therapy].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Targeting amino acid in tumor therapy.Frontiers in oncology · 2025
    Review
  8. Article
  9. Review
  10. Review
  11. FOXO3: at the crossroads of metabolic, inflammatory, and tumorigenic remodeling in the colon.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Review
  12. International journal of molecular sciences · 2023
    Article
  13. The crisscross between p53 and metabolism in cancer.Acta biochimica et biophysica Sinica · 2023
    Review
  14. Review
  15. Protective Effects ofInternational journal of molecular sciences · 2023
    Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Mechanistic roles of mutant p53 governing lipid metabolism.Advances in biological regulation · 2022
    Review

2 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

2 authors at 2 institutions in 1 country.

Alejandro ParralesDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA. aparrales@kumc.edu.
Tomoo IwakumaDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA. tiwakuma@kumc.edu.
The University of Kansas Cancer Center · USUniversity of Kansas Medical Center · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
The role of MDM2-MTBP axis in cancer metastasisR01CA174735 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI IWAKUMA, TOMOO · 2014 to 2018
$1.6M
NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA174735
6 · The paper itself

Abstract

Enhanced proliferation and survival are common features of cancer cells. Cancer cells are metabolically reprogrammed which aids in their survival in nutrient-poor environments. Indeed, changes in metabolism of glucose and glutamine are essential for tumor progression. Thus, metabolic reprogramming is now well accepted as a hallmark of cancer. Recent findings suggest that reprogramming of lipid metabolism also occurs in cancer cells, since lipids are used for biosynthesis of membranes, post-translational modifications, second messengers for signal transduction, and as a source of energy during nutrient deprivation. The tumor suppressor p53 is a transcription factor that controls the expression of proteins involved in cell cycle arrest, DNA repair, apoptosis, and senescence. p53 also regulates cellular metabolism, which appears to play a key role in its tumor suppressive activities. In this review article, we summarize non-canonical functions of wild-type and mutant p53 on lipid metabolism and discuss their association with cancer progression.

Indexed as

Lipid MetabolismAnimalsHumansMutant ProteinsNeoplasm ProteinsNeoplasmsTumor Suppressor Protein p53Mutant ProteinsNeoplasm ProteinsTumor Suppressor Protein p53cancerfatty acid oxidationlipid metabolismmevalonate pathwayp53

Identifiers

PMID27973397
PMCPMC5187874
OpenAlexW2563331414

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.