Evidence map›Paper›PMID 27872580›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2016

Untargeted polar metabolomics of transformed MDA-MB-231 breast cancer cells expressing varying levels of human arylamine

Samantha M Carlisle, Patrick J Trainor, Xinmin Yin, Mark A Doll, Marcus W Stepp, J Christopher States, Xiang Zhang, David W Hein

Open access · greenAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Proteomic analysis of arylamineToxicology reports · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Journal of oncology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Untargeted and stable isotope-assisted metabolomic analysis of MDA-MB-231 cells under hypoxia.Metabolomics : Official journal of the Metabolomic Society · 2018
    Article
  12. Article
  13. Article
  14. Altered Levels ofIn vivo (Athens, Greece)
    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

8 authors at 2 institutions in 1 country.

Samantha M CarlisleDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Patrick J TrainorDepartment of Cardiovascular Medicine, University of Louisville, Louisville, KY 40292, USA.
Xinmin YinDepartment of Chemistry, University of Louisville, Louisville, KY 40292, USA.
Mark A DollDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Marcus W SteppDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
J Christopher StatesDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
Xiang ZhangDepartment of Chemistry, University of Louisville, Louisville, KY 40292, USA.
David W HeinDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA.
University of Louisville · USKosair Charities · US

Funding

UOFL ENVIRONMENTAL HEALTH SCIENCES TRAINING PROGRAMT32ES011564 · NIEHS · UNIVERSITY OF LOUISVILLE · PI David W Hein, John Pierce Wise · 2004 to 2026
$7.1M
PHARMACOGENETICS OF DRUG &CARCINOGEN METABOLISMR01CA034627 · NCI · UNIVERSITY OF NORTH DAKOTA · PI HEIN, DAVID W · 1985 to 2009
$3.1M
NCI NIH HHS R01 CA034627NIEHS NIH HHS T32 ES011564
6 · The paper itself

Abstract

introductionHuman arylamine

objectiveThis study explored polar metabolome differences between MDA-MB-231 breast cancer cells expressing varying levels of NAT1 activity using an untargeted approach.

methodsThree MDA-MB-231 breast adenocarcinoma cell lines that stably express wild-type, increased, and decreased levels of human NAT1 were investigated for differences in polar metabolic profile using a comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry (GC×GC-TOF MS) system.

resultsIncreased levels of human NAT1 in the transformed cell lines resulted in a statistically significant decreased abundance of the metabolite palmitoleic acid (q = 0.0006), when compared to normal and decreased levels of human NAT1. The fatty acid synthesis pathway utilizes acetyl coenzyme A (acetyl-CoA) in the first two reactions of the pathway and eventually leads to the synthesis of palmitoleic acid.

conclusionThese data suggest a link between increased levels of NAT1 activity and decreased flux of acetyl-CoA through this portion of the fatty acid synthesis pathway.

Indexed as

Acetyl-CoABreast CancerMetabolomicsNAT1Palmitoleic Acid

Identifiers

PMID27872580
PMCPMC5115175
OpenAlexW2473336206

What OpenQuestion holds

Textmetadata
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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.