Evidence map›Paper›PMID 26022278›Full record

ArticleArthritis research & therapy2015

KIAA1199 as a potential diagnostic biomarker of rheumatoid arthritis related to angiogenesis.

Xinyu Yang, Pengcheng Qiu, Bingbing Chen, Yaoyao Lin, Zhonghao Zhou, Renshan Ge, Hai Zou, Jianmin Wang, Jianguang Wang

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

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  16. Global molecular changes in a tibial compression induced ACL rupture model of post-traumatic osteoarthritis.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2017
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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

9 authors at 2 institutions in 1 country.

Xinyu YangDepartment of Medicinal Chemistry, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China. cyrillyoung@163.com.
Pengcheng QiuDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. 347004915@qq.com.
Bingbing ChenDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. 738877136@qq.com.
Yaoyao LinDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. 398560338@qq.com.
Zhonghao ZhouDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. 475634534@qq.com.
Renshan GeDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. 1729844779@qq.com.
Hai ZouDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. 512586826@qq.com.
Jianmin WangDepartment of Rheumatology, Jiamusi Central Hospital, Jiamusi, China. wangjiangmin1968@126.com.
Jianguang WangDepartment of Biochemistry, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China. wz_wjg@163.com.
Wenzhou Medical University · CNJiamusi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOur previous proteomic study on fibroblast-like synoviocytes (FLSs) derived from the synovial tissues found that the expression of KIAA1199 was higher in rheumatoid arthritis (RA) patients than in healthy controls. The aim of this study was to examine the biological function of KIAA1199 and evaluate its clinical diagnosis value in RA.

methodsThe over-expression of KIAA1199 was verified by quantitative real-time polymerase chain reaction (qPCR), Immunohistochemistry, Immunofluorescence and enzyme linked immunosorbent assay (ELISA) in inactive and active RA patients and healthy controls. The effect of KIAA1199 expression on FLSs proliferation, angiogenesis and related pathway were analyzed by MTT, cell migration, tube formation, chorioallantoic membrane (CAM) assay, qPCR and western-blotting after KIAA1199 knockdown and over-expression.

resultsThe verification results show the up-regulation of KIAA1199 in RA patients at mRNA and protein level as compared to that in healthy controls. ELISA and receiver operator characteristic (ROC) analysis shows that KIAA1199 concentration in serum, synovial fluid and synovial tissues could be used as dependable biomarkers for the diagnosis of active RA, provided an area under roc curve (AUC) of 0.83, 0.92 and 0.92. Sensitivity and specificity, which were determined by cut-off points, reached 72% 84% and 80% in sensitivity and 80%, 93.3%, 93.3% in specificity, respectively. Moreover, KIAA1199 also enhance the proliferation and angiogenesis of synovial membrane, and KIAA1199/ PLXNB3/ SEMA5A/CTGF axis may be a newly found pathway enhancing cell proliferation and angiogenesis.

conclusionKIAA1199 may be a potential diagnostic biomarker of RA related to angiogenesis.

Indexed as

Area Under CurveArthritis, RheumatoidBiomarkersBlotting, WesternEnzyme-Linked Immunosorbent AssayFemaleHumansHyaluronoglucosaminidaseImmunohistochemistryMaleMiddle AgedNeovascularization, PathologicProteinsReal-Time Polymerase Chain ReactionROC CurveSensitivity and SpecificityBiomarkersCEMIP protein, humanHyaluronoglucosaminidaseProteins

Identifiers

PMID26022278
PMCPMC4448531
OpenAlexW1584234966

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.