Evidence map›Paper›PMID 30572452›Full record

ArticleMedicine2018

FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases.

Li Li, Xiaoying Wu, Eerdunchaolu, Wenyan Qin, Yuqiu Yang, Geriletu Wang, Huili He, Husileng Zhang

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 84% of its field
1 · What the graph read from it

What it found

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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

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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 2 countries.

Li LiDepartment of Traditional Mongolian Medical Encephalopathy, Affiliated Hospital of Inner Mongolia University for the Nationalities, Tongliao City, Inner Mongolia Autonomous Region.
Xiaoying WuCollege of Traditional Mongolian Medicine and Pharmacology, Inner Mongolia University for the Nationalities, Tongliao City, The Inner Mongolia Autonomous Region.
EerdunchaoluCollege of Traditional Mongolian Medicine and Pharmacology, Inner Mongolia University for the Nationalities, Tongliao City, The Inner Mongolia Autonomous Region.
Wenyan QinScientific research division, Beijing CapitalBio Technology Co., LTD., Beijing.
Yuqiu YangDepartment of Traditional Mongolian Medical Intrusive Encephalopathy, Affiliated Hospital of Inner Mongolia University for the Nationalities, Tongliao City, Inner Mongolia Autonomous Region, PR China.
Geriletu WangCollege of Traditional Mongolian Medicine and Pharmacology, Inner Mongolia University for the Nationalities, Tongliao City, The Inner Mongolia Autonomous Region.
Huili HeCollege of Traditional Mongolian Medicine and Pharmacology, Inner Mongolia University for the Nationalities, Tongliao City, The Inner Mongolia Autonomous Region.
Husileng ZhangDepartment of Traditional Mongolian Medical Intrusive Encephalopathy, Affiliated Hospital of Inner Mongolia University for the Nationalities, Tongliao City, Inner Mongolia Autonomous Region, PR China.
National University of Mongolia · MNCapital University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfluenza, measles, and mumps are common viral infectious diseases in Mongolia. The traditional Mongolian medicine (TMM) classified them as warm disease, and still plays a major role in the diagnoses and treatments.

methodsTo interpret the connotation of the complex theoretical system in TMM with scientific technique, in this study, a high throughput mass spectrometry was used to identify potential protein markers of TMM symptom types. Fifty venous blood samples were drawn from influenza, measles and mumps patients. Differential proteins between samples of patients diagnosed as immature and mature heat in TMM were detected by mass spectrometry.

resultsAfter proteomics analysis, 1500 proteins and 7619 polypeptides were identified and 1323 in total showed differential expression between those 2 symptom types; then enrichment analysis of the differentially expressed proteins revealed the significant biological functions related to the differentially expressed proteins, including cardiomyopathy, several bacterial and parasitic infections, bacterial invasion of epithelial cells, insulin signaling pathway, and regulation of actin cytoskeleton. The network analysis showed that FBP2 and Talin-1 were critical points and might determine the evolution directions of TMM warm disease symptom.

conclusionsThis study suggests that the identified core differential proteins may be regarded as potential biomarkers, and benefit to evaluate the evolutionary tendency of TMM warm disease symptoms.

Indexed as

AdolescentAdultAgedBiomarkersFructose-BisphosphataseHigh-Throughput Screening AssaysHumansInfluenza, HumanMass SpectrometryMeaslesMedicine, Mongolian TraditionalMiddle AgedMumpsProteomicsTalinYoung AdultBiomarkersFructose-BisphosphataseTalinTLN1 protein, human

Identifiers

PMID30572452
PMCPMC6320185
OpenAlexW2905892070

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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.