Evidence map›Paper›PMID 22298307›Full record

ArticleMolecular & cellular proteomics : MCP2012

Identification of candidate biomarkers for early detection of human lung squamous cell cancer by quantitative proteomics.

Gu-Qing Zeng, Pang-Fei Zhang, Xingming Deng, Feng-Lei Yu, Cui Li, Yan Xu, Hong Yi, Mao-Yu Li, Rong Hu, Jian-Hong Zuo and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-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

37 citing papers in PubMed, 68 citations in OpenAlex.

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  8. Serum Proteomic Profiling Analysis of Rats Chronically Exposed to Arsenic.Medical science monitor : international medical journal of experimental and clinical research · 2019
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  19. Expression Profiling ofIranian journal of biotechnology · 2017
    Article
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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

19 authors at 4 institutions in 2 countries.

Gu-Qing ZengKey Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha 410008, China.
Pang-Fei Zhang
Xingming Deng
Feng-Lei Yu
Cui Li
Yan Xu
Hong Yi
Mao-Yu Li
Rong Hu
Jian-Hong Zuo
Xin-Hui Li
Xun-Xun Wan
Jia-Quan Qu
Qiu-Yan He
Jian-Huang Li
Xu Ye
Yu Chen
Jiao-Yang Li
Zhi-Qiang Xiao
Xiangya Hospital Central South University · CNCentral South University · CNEmory University · USSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To discover novel biomarkers for early detection of human lung squamous cell cancer (LSCC) and explore possible mechanisms of LSCC carcinogenesis, iTRAQ-tagging combined with two dimensional liquid chromatography tandem MS analysis was used to identify differentially expressed proteins in human bronchial epithelial carcinogenic process using laser capture microdissection-purified normal bronchial epithelium (NBE), squamous metaplasia (SM), atypical hyperplasia (AH), carcinoma in situ (CIS) and invasive LSCC. As a result, 102 differentially expressed proteins were identified, and three differential proteins (GSTP1, HSPB1 and CKB) showing progressively expressional changes in the carcinogenic process were selectively validated by Western blotting. Immunohistochemistry was performed to detect the expression of the three proteins in an independent set of paraffin-embedded archival specimens including various stage tissues of bronchial epithelial carcinogenesis, and their ability for early detection of LSCC was evaluated by receiver operating characteristic analysis. The results showed that the combination of the three proteins could perfectly discriminate NBE from preneoplastic lesions (SM, AH and CIS) from invasive LSCC, achieving a sensitivity of 96% and a specificity of 92% in discriminating NBE from preneoplatic lesions, a sensitivity of 100% and a specificity of 98% in discriminating NBE from invasive LSCC, and a sensitivity of 92% and a specificity of 91% in discriminating preneoplastic lesions from invasive LSCC, respectively. Furthermore, we knocked down GSTP1 in immortalized human bronchial epithelial cell line 16HBE cells, and then measured their susceptibility to carcinogen benzo(a)pyrene-induced cell transformation. The results showed that GSTP1 knockdown significantly increased the efficiency of benzo(a)pyrene-induced 16HBE cell transformation. The present data first time show that GSTP1, HSPB1 and CKB are novel potential biomarkers for early detection of LSCC, and GSTP1 down-regulation is involved in human bronchial epithelial carcinogenesis.

Indexed as

Early Detection of CancerAmino Acid SequenceBiomarkers, TumorBronchiCell LineCell Transformation, NeoplasticCluster AnalysisCreatine Kinase, BB FormEpithelial CellsGene ExpressionGlutathione S-Transferase piHeat-Shock ProteinsHSP27 Heat-Shock ProteinsHumansLaser Capture MicrodissectionLung NeoplasmsBiomarkers, TumorCreatine Kinase, BB FormGlutathione S-Transferase piGSTP1 protein, humanHeat-Shock ProteinsHSP27 Heat-Shock ProteinsHSPB1 protein, humanMolecular Chaperones

Identifiers

PMID22298307
PMCPMC3433890
OpenAlexW2114516399

What OpenQuestion holds

Textmetadata
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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.