Evidence map›Paper›PMID 35742953›Full record

ArticleInternational journal of molecular sciences2022

Tissue-Specific Downregulation of Fatty Acid Synthase Suppresses Intestinal Adenoma Formation via Coordinated Reprograming of Transcriptome and Metabolism in the Mouse Model of Apc-Driven Colorectal Cancer.

James Drury, Lyndsay E A Young, Timothy L Scott, Courtney O Kelson, Daheng He, Jinpeng Liu, Yuanyan Wu, Chi Wang, Heidi L Weiss, Teresa Fan and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Potential Application Value of FASN in the Diagnosis of Colorectal Cancer.JGH open : an open access journal of gastroenterology and hepatology · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
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

13 authors at 1 institution in 1 country.

James DruryDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40536, USA.
Lyndsay E A YoungDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0002-6873-5674
Timothy L ScottMarkey Cancer Center, University of Kentucky, Lexington, KY 40536, USA.
Courtney O KelsonDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0002-5728-8557
Daheng HeMarkey Cancer Center Biostatistics and Bioinformatics Shared Resource Facility, University of Kentucky, Lexington, KY 40536, USA.
Jinpeng LiuMarkey Cancer Center Biostatistics and Bioinformatics Shared Resource Facility, University of Kentucky, Lexington, KY 40536, USA.
Yuanyan WuMarkey Cancer Center Biostatistics and Bioinformatics Shared Resource Facility, University of Kentucky, Lexington, KY 40536, USA.
Chi WangMarkey Cancer Center Biostatistics and Bioinformatics Shared Resource Facility, University of Kentucky, Lexington, KY 40536, USA.
Heidi L WeissMarkey Cancer Center Biostatistics and Bioinformatics Shared Resource Facility, University of Kentucky, Lexington, KY 40536, USA.
Teresa FanDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0002-7292-8938
Matthew S GentryDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0001-5253-9049
Ramon SunMarkey Cancer Center, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0002-3009-1850
Yekaterina Y ZaytsevaDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0003-2641-9363
University of Kentucky · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
University of Kentucky Center for Cancer MetabolismP20GM121327 · NIGMS · UNIVERSITY OF KENTUCKY · PI Jianhang Jia · 2017 to 2026
$25.0M
Brain Glycogen-Metabolism,Mechanisms, and Therapeutic PotentialR35NS116824 · NINDS · UNIVERSITY OF KENTUCKY · PI Matthew S. Gentry · 2020 to 2026
$8.2M
Interdisciplinary Research Training in Cancer BiologyT32CA165990 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers, KATHLEEN L. O'CONNOR · 2013 to 2026
$3.2M
Aberrant Glycogen Modulates Cerebral Glucose Metabolism in Aging and Alzheimer's DiseaseR01AG066653 · NIA · UNIVERSITY OF KENTUCKY · PI SUN, RAMON C. · 2020 to 2024
$1.9M
Targeting Lipid Metabolism in Colorectal CancerR01CA249734 · NCI · UNIVERSITY OF KENTUCKY · PI ZAYTSEVA, YEKATERINA · 2021 to 2025
$1.7M
Fatty acid synthase in regulation of UDP-GlcNAc synthesis in colorectal cancerR03CA262720 · NCI · UNIVERSITY OF KENTUCKY · PI ZAYTSEVA, YEKATERINA · 2021 to 2022
$153k
NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA249734NCI NIH HHS R01 CA249734, R03 CA262720NCI NIH HHS R03 CA262720NCI NIH HHS T32 CA165990NIA NIH HHS R01 AG066653NIGMS NIH HHS P20 GM121327NIH HHS R01 AG066653NINDS NIH HHS R35 NS116824
6 · The paper itself

Abstract

Altered lipid metabolism is a potential target for therapeutic intervention in cancer. Overexpression of Fatty Acid Synthase (FASN) correlates with poor prognosis in colorectal cancer (CRC). While multiple studies show that upregulation of lipogenesis is critically important for CRC progression, the contribution of FASN to CRC initiation is poorly understood. We utilize a C57BL/6-Apc/Villin-Cre mouse model with knockout of FASN in intestinal epithelial cells to show that the heterozygous deletion of FASN increases mouse survival and decreases the number of intestinal adenomas. Using RNA-Seq and gene set enrichment analysis, we demonstrate that a decrease in FASN expression is associated with inhibition of pathways involved in cellular proliferation, energy production, and CRC progression. Metabolic and reverse phase protein array analyses demonstrate consistent changes in alteration of metabolic pathways involved in both anabolism and energy production. Downregulation of FASN expression reduces the levels of metabolites within glycolysis and tricarboxylic acid cycle with the most significant reduction in the level of citrate, a master metabolite, which enhances ATP production and fuels anabolic pathways. In summary, we demonstrate the critical importance of FASN during CRC initiation. These findings suggest that targeting FASN is a potential therapeutic approach for early stages of CRC or as a preventive strategy for this disease.

Indexed as

AdenomaColorectal NeoplasmsAnimalsCell Line, TumorDisease Models, AnimalDown-RegulationFatty Acid SynthasesFatty Acid Synthase, Type IMiceMice, Inbred C57BLTranscriptomeFatty Acid SynthasesFatty Acid Synthase, Type IApc mutationcolorectal cancercolorectal cancer initiationfatty acid synthaselipid metabolism

Identifiers

PMID35742953
PMCPMC9245602
OpenAlexW4281688484

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.