Evidence map›Paper›PMID 27153558›Full record

ArticleOncotarget2016

Plasma lipidomics profiling identified lipid biomarkers in distinguishing early-stage breast cancer from benign lesions.

Xiaoli Chen, Hankui Chen, Meiyu Dai, Junmei Ai, Yan Li, Brett Mahon, Shengming Dai, Youping Deng

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

64 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
  4. Article
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  6. Article
  7. Lipids: Driving Forces in the Underlying Biology of Carcinogenesis.ACS pharmacology & translational science · 2025
    Review
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  20. Synthesis of ether lipids: natural compounds and analogues.Beilstein journal of organic chemistry · 2023
    Review

4 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

8 authors.

Xiaoli ChenDepartment of Clinical Laboratory, The Fourth Hospital Affiliated to Guangxi Medical University, Liuzhou City, Guangxi Province, China.
Hankui ChenDepartment of Medicine, Rush University Medical Center, Chicago, Illinois, USA.
Meiyu DaiDepartment of Clinical Laboratory, The Fourth Hospital Affiliated to Guangxi Medical University, Liuzhou City, Guangxi Province, China.
Junmei AiDepartment of Medicine, Rush University Medical Center, Chicago, Illinois, USA.
Yan LiDepartment of Medicine, Rush University Medical Center, Chicago, Illinois, USA.
Brett MahonDepartment of Pathology, Rush University Medical Center, Chicago, Illinois, USA.
Shengming DaiDepartment of Clinical Laboratory, The Fourth Hospital Affiliated to Guangxi Medical University, Liuzhou City, Guangxi Province, China.
Youping DengDepartment of Medicine, Rush University Medical Center, Chicago, Illinois, USA.

Funding

RESEARCH DESIGN AND BIOSTATISTICS COREU54MD007584 · NIMHD · UNIVERSITY OF HAWAII AT MANOA · PI HEDGES, JERRIS ROBERT, MOKUAU, NOREEN · 2012 to 2018
$21.1M
EARLY DETECTION OF LUNG CANCER USING METABOLOMIC LIPID PROFILINGR21CA164764 · NCI · RUSH UNIVERSITY MEDICAL CENTER · PI DENG, YOUPING · 2013 to 2014
$360k
NCI NIH HHS R21 CA164764NIMHD NIH HHS U54 MD007584
6 · The paper itself

Abstract

backgroundBreast cancer is very common and highly fatal in women. Current non-invasive detection methods like mammograms are unsatisfactory. Lipidomics, a promising detection method, may serve as a novel prognostic approach for breast cancer in high-risk patients.

resultsAccording the predictive model, the combination of 15 lipid species had high diagnostic value. In the training set, sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the combination of these 15 lipid species were 83.3%, 92.7%, 89.7%, and 87.9%, respectively. The AUC in the training set was 0.926 (95% CI 0.869-0.982). Similar results were found in the validation set, with the sensitivity, specificity, PPV and NPV at 81.0%, 94.5%, 91.9%, and 86.7%, respectively. The AUC was 0.938 (95% CI 0.889-0.986) in the validation set.

methodsUsing triple quadrupole liquid chromatography electrospray ionization tandem mass spectrometry, this study was to detect global lipid profiling of a total of 194 plasma samples from 84 patients with early-stage breast cancer (stage 0-II) and 110 patients with benign breast disease included in a training set and a validation set. A binary logistic regression was used to build a predictive model for evaluating the lipid species as potential biomarkers in the diagnosis of breast cancer.

conclusionsThe combination of these 15 lipid species as a panel could be used as plasma biomarkers for the diagnosis of breast cancer.

Indexed as

AdultAgedBiomarkers, TumorBreast DiseasesBreast NeoplasmsChromatography, LiquidDiagnosis, DifferentialFemaleHumansLipidsMiddle AgedNeoplasm StagingPrognosisReproducibility of ResultsROC CurveTandem Mass SpectrometryBiomarkers, TumorLipidsbenign lesionbiomarkerbreast cancerlipidomicsplasma

Identifiers

PMID27153558
PMCPMC5095026

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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.