Evidence map›Paper›PMID 29021294›Full record

ArticleMolecular & cellular proteomics : MCP2017

Identification of Serological Biomarkers for Early Diagnosis of Lung Cancer Using a Protein Array-Based Approach.

Jianbo Pan, Guang Song, Dunyan Chen, Yadong Li, Shuang Liu, Shaohui Hu, Christian Rosa, Daniel Eichinger, Ignacio Pino, Heng Zhu and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

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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

12 authors at 6 institutions in 3 countries.

Jianbo PanFrom the ‡Department of Ophthalmology, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.
Guang Song§Department of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.
Dunyan Chen¶Provincial Clinical College, Fujian Medical University, Fuzhou 350001, Fujian, China.
Yadong Li¶Provincial Clinical College, Fujian Medical University, Fuzhou 350001, Fujian, China.
Shuang Liu§Department of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.
Shaohui Hu**CDI Laboratories, Inc., Mayaguez, Puerto Rico 00682.
Christian Rosa**CDI Laboratories, Inc., Mayaguez, Puerto Rico 00682.
Daniel Eichinger**CDI Laboratories, Inc., Mayaguez, Puerto Rico 00682.
Ignacio Pino**CDI Laboratories, Inc., Mayaguez, Puerto Rico 00682.
Heng Zhu§Department of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland 21205; hyi8070@126.com jiang.qian@jhmi.edu hzhu4@jhmi.edu.
Jiang QianFrom the ‡Department of Ophthalmology, Johns Hopkins School of Medicine, Baltimore, Maryland 21205; hyi8070@126.com jiang.qian@jhmi.edu hzhu4@jhmi.edu.
Yi Huang¶Provincial Clinical College, Fujian Medical University, Fuzhou 350001, Fujian, China; hyi8070@126.com jiang.qian@jhmi.edu hzhu4@jhmi.edu.
CDI Laboratories (United States) · PRJohns Hopkins Medicine · USFujian Medical University · CNFujian Provincial Hospital · CNJohns Hopkins University · USSidney Kimmel Comprehensive Cancer Center · US

Funding

Proteome Characterization Center: A Genoproteomics Pipeline for Cance ResearchU24CA160036 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHAN, DANIEL WANYUI, ZHANG, HUI · 2011 to 2016
$10.7M
NCI NIH HHS U24 CA160036
6 · The paper itself

Abstract

Lung cancer (LC) remains the leading cause of mortality from malignant tumors worldwide. Currently, a lack of serological biomarkers for early LC diagnosis is a major roadblock for early intervention and prevention of LC. To undertake this challenge, we employed a two-phase strategy to discover and validate a biomarker panel using a protein array-based approach. In Phase I, we obtained serological autoimmune profiles of 80 LC patients and 20 healthy subjects on HuProt arrays, and identified 170 candidate proteins significantly associated with LC. In Phase II, we constructed a LC focused array with the 170 proteins, and profiled a large cohort, comprised of 352 LC patients, 93 healthy individuals, and 101 patients with lung benign lesions (LBL). The comparison of autoimmune profiles between the early stage LC and the combined group of healthy and LBL allowed us to identify and validate a biomarker panel of p53, HRas, and ETHE1 for diagnosis of early stage LC with 50% sensitivity at >90% specificity. Finally, the performance of this biomarker panel was confirmed in ELISA tests. In summary, this study represents one of the most comprehensive proteome-wide surveys with one of the largest (

Indexed as

AgedAutoantibodiesAutoimmunityBiomarkers, TumorCase-Control StudiesEarly Detection of CancerFemaleHumansLung NeoplasmsMaleMiddle AgedMitochondrial ProteinsNucleocytoplasmic Transport ProteinsProtein Array AnalysisProto-Oncogene Proteins p21(ras)Sensitivity and SpecificityAutoantibodiesBiomarkers, TumorETHE1 protein, humanHRAS protein, humanMitochondrial ProteinsNucleocytoplasmic Transport ProteinsProto-Oncogene Proteins p21(ras)TP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID29021294
PMCPMC5724172
OpenAlexW2761050422

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.