Evidence map›Paper›PMID 22628229›Full record

ArticleJournal of clinical laboratory analysis2012

Identification of novel low molecular weight serum peptidome biomarkers for non-small cell lung cancer (NSCLC).

Juan Yang, Yong-Chun Song, Tu-Sheng Song, Xiao-Yan Hu, You-Min Guo, Zong-Fang Li, Cheng-Xue Dang, Chen Huang

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Article in Journal of clinical laboratory analysis, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
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1 · What the graph read from it

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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

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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

11 citing papers in PubMed.

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  7. Identification of peptide regions of SERPINA1 and ENOSF1 and their protein expression as potential serum biomarkers for gastric cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Juan YangDepartment of Genetics and Molecular Biology, Medical school of Xi'an Jiaotong University /Key Laboratory of Environment and Disease-Related Gene, Ministry of Education, PR China.
Yong-Chun Song
Tu-Sheng Song
Xiao-Yan Hu
You-Min Guo
Zong-Fang Li
Cheng-Xue Dang
Chen Huang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo identify discriminating protein patterns in serum samples among non-small cell lung cancer (NSCLC), chronic obstructive pulmonary disease (COPD), pneumonia, and healthy controls. To discover specific low molecular weight (LMW) serum peptidome biomarkers and establish a diagnostic pattern for NSCLCby using proteomic technology.

methodsWe used magnetic bead-based separation followed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) to identify patients with NSCLC, COPD, and pneumonia. A total of 154 serum samples were analyzed in this study, among which there were 60 serum samples from NSCLC patients, 30 from patients with other lung-related diseases (16 pneumonia patients and 14 patients with COPD) as disease controls, and 64 from healthy volunteers as healthy control. The mass spectra, analyzed using ClinProTools software, distinguished between cancer patients and healthy individuals based on GA algorithm model.

resultsIn this study, we generated numerous discriminating m/z peaks as well as disease-specific discrimination peaks. A set of five potential biomarkers (m/z: 7,763.24, 1,012.61, 4,153.16, 1,450.55, and 2,878.89) could be used as the diagnostic biomarkers to distinguish NSCLCpatients from healthy controls. In the training set, patients with NSCLC could be identified with sensitivity of 97.5% and specificity of 98.8%. Similar results were obtained in the testing set, showing 80.7% sensitivity and 91.2% specificity.

conclusionOur study demonstrated that a combined application of magnetic beads with MALDI-TOF MS technique was suitable for identification of serum biomarkers for NSCLC.

Indexed as

AlgorithmsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCase-Control StudiesHumansLung NeoplasmsMolecular WeightPeptidesPneumoniaProteomeProteomicsPulmonary Disease, Chronic ObstructiveSensitivity and SpecificitySpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationBiomarkers, TumorPeptidesProteome

Identifiers

PMID22628229
PMCPMC6807414

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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.