Evidence map›Paper›PMID 36893152›Full record

ArticlePloS one2023

Effects of β-caryophyllene and oxygen availability on cholesterol and fatty acids in breast cancer cells.

Christopher J Frost, Andrea Ramirez-Mata, Ram B Khattri, Matthew E Merritt, Susan C Frost

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

5 authors at 2 institutions in 1 country.

Christopher J FrostBIO5 Institute, University of Arizona, Tucson, AZ, United States of America.ORCID 0000-0001-5986-8646
Andrea Ramirez-MataDepartment of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Ram B KhattriDepartment of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.ORCID 0000-0001-9991-263X
Matthew E MerrittDepartment of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Susan C FrostDepartment of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.ORCID 0000-0002-2020-097X
University of Florida · USUniversity of Arizona · US

Funding

Southeast Resource Center for Integrated Metabolomics (SECIM)U24DK097209 · NIDDK · UNIVERSITY OF FLORIDA · PI YOST, RICHARD A. · 2013 to 2017
$9.2M
TR&D3-SCHP41GM122698 · NIGMS · FLORIDA STATE UNIVERSITY · PI BREY, WILLIAM W, CROSS, TIMOTHY A · 2017 to 2021
$6.7M
National Resource for Advanced NMR TechnologyRM1GM148766 · NIGMS · FLORIDA STATE UNIVERSITY · PI William W Brey, Joanna R Long · 2023 to 2026
$4.9M
NIDDK NIH HHS U24 DK097209NIGMS NIH HHS P41 GM122698NIGMS NIH HHS RM1 GM148766
6 · The paper itself

Abstract

Hypoxia is a common feature of most solid tumors, one that favors tumor progression and limits treatment effectiveness. Targeting hypoxia has long been a goal in cancer therapy, by identifying factors that reverse or ameliorate the effects of hypoxia on cancer cells. We, and others, have shown that β-caryophyllene (BCP) exhibits anti-proliferative properties in cancer cells. We have further shown that non-cytotoxic concentrations of BCP affect cholesterol and lipid biosynthesis in hypoxic hBrC cells at both transcriptional and translational levels. This led us to hypothesize that BCP may reverse the hypoxic phenotype in hBrC cells. To test this, we determined the effect of BCP on hypoxic sensitive pathways, including oxygen consumption, glycolysis, oxidative stress, cholesterol and fatty acid biosynthesis, and ERK activation. While each of these studies revealed new information on the regulation by hypoxia and BCP, only the lipidomic studies showed reversal of hypoxic-dependent effects by BCP. These later studies showed that hypoxia-treated samples lowered monounsaturated fatty acid levels, shifting the saturation ratios of the fatty acid pools. This signature was ameliorated by sub-lethal concentrations of BCP, possibly through an effect on the C:16 fatty acid saturation ratios. This is consistent with BCP-induced upregulation of the stearoyl-CoA desaturase (SCD) gene, observed previously. This suggests that BCP may interfere with the lipid signature modulated by hypoxia which could have consequences for membrane biosynthesis or composition, both of which are important for cell replication.

Indexed as

Fatty AcidsNeoplasmsCholesterolHumansHypoxiaOxygenPolycyclic SesquiterpenesStearoyl-CoA DesaturasecaryophylleneCholesterolFatty AcidsOxygenPolycyclic SesquiterpenesStearoyl-CoA Desaturase

Identifiers

PMID36893152
PMCPMC9997903
OpenAlexW4323652754

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.