Evidence map›Paper›PMID 28167702›Full record

ArticleJournal of lipid research2017

Assessment of altered lipid homeostasis by HILIC-ion mobility-mass spectrometry-based lipidomics.

Kelly M Hines, Josi Herron, Libin Xu

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.3field-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

41 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Article
  3. Application of Ion Mobility Mass Spectrometry in Lipidomics.Advances in experimental medicine and biology · 2026
    Review
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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

3 authors at 1 institution in 1 country.

Kelly M HinesDepartment of Medicinal Chemistry University of Washington, Seattle, WA 98195.
Josi HerronDepartment of Medicinal Chemistry University of Washington, Seattle, WA 98195; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195.
Libin XuDepartment of Medicinal Chemistry University of Washington, Seattle, WA 98195; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195. Electronic address: libinxu@uw.edu.
University of Washington · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
Environmetal Pathology/Toxicology Training ProgramT32ES007032 · NIEHS · UNIVERSITY OF WASHINGTON · PI FAUSTMAN, ELAINE M, ROSENFELD, MICHAEL E · 1985 to 2023
$10.7M
7-Dehydrocholesterol-derived oxysterols in SLOS: role and therapyR00HD073270 · NICHD · UNIVERSITY OF WASHINGTON · PI XU, LIBIN · 2015 to 2017
$745k
NICHD NIH HHS R00 HD073270NIEHS NIH HHS P30 ES007033NIEHS NIH HHS T32 ES007032
6 · The paper itself

Abstract

Ion mobility-mass spectrometry (IM-MS) has proven to be a highly informative technique for the characterization of lipids from cells and tissues. We report the combination of hydrophilic-interaction liquid chromatography (HILIC) with traveling-wave IM-MS (TWIM-MS) for comprehensive lipidomics analysis. Main lipid categories such as glycerolipids, sphingolipids, and glycerophospholipids are separated on the basis of their lipid backbones in the IM dimension, whereas subclasses of each category are mostly separated on the basis of their headgroups in the HILIC dimension, demonstrating the orthogonality of HILIC and IM separations. Using our previously established lipid calibrants for collision cross-section (CCS) measurements in TWIM, we measured over 250 CCS values covering 12 lipid classes in positive and negative modes. The coverage of the HILIC-IM-MS method is demonstrated in the analysis of Neuro2a neuroblastoma cells exposed to benzalkonium chlorides (BACs) with C10 or C16 alkyl chains, which we have previously shown to affect gene expression related to cholesterol and lipid homeostasis. We found that BAC exposure resulted in significant changes to several lipid classes, including glycerides, sphingomyelins, phosphatidylcholines, and phosphatidylethanolamines. Our results indicate that BAC exposure modifies lipid homeostasis in a manner that is dependent upon the length of the BAC alkyl chain.

Indexed as

Benzalkonium CompoundsCholesterolChromatography, LiquidGene Expression RegulationHomeostasisHumansHydrophobic and Hydrophilic InteractionsLipid MetabolismLipidsMass SpectrometryMetabolic Networks and PathwaysBenzalkonium CompoundsCholesterolLipidsAY9944benzalkonium chloridecholesterol/biosynthesiscollision cross-sectionhydrophilic interaction liquid chromatographyliquid chromatographyneuro2a cellsphospholipids

Identifiers

PMID28167702
PMCPMC5392737
OpenAlexW2586272172

What OpenQuestion holds

Textmetadata
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.