Evidence map›Paper›PMID 26768647›Full record

ArticleCellular and molecular neurobiology2016

Leukocyte Gene Expression and Plasma Concentration in Multiple Sclerosis: Alteration of Transforming Growth Factor-βs, Claudin-11, and Matrix Metalloproteinase-2.

Gholamreza Hassanzadeh, Samaneh Hosseini Quchani, Mohammad Ali Sahraian, Farid Abolhassani, Mohammad Ali Sadighi Gilani, Masoomeh Dehghan Tarzjani, Fatemeh Atoof

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In one paragraph

Article in Cellular and molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  5. Review
  6. The rs3761548 FOXP3 variant is associated with multiple sclerosis and transforming growth factor β1 levels in female patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Article
  7. 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

7 authors at 2 institutions in 1 country.

Gholamreza HassanzadehDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Poursina Avenue, 1417613151, Tehran, Iran.
Samaneh Hosseini QuchaniDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Poursina Avenue, 1417613151, Tehran, Iran. b.s.hoseini@gmail.com.ORCID http://orcid.org/0000-0002-6129-8467
Mohammad Ali SahraianDepartment of Neurology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Farid AbolhassaniDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Poursina Avenue, 1417613151, Tehran, Iran.
Mohammad Ali Sadighi GilaniDepartment of Urology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Masoomeh Dehghan TarzjaniDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Poursina Avenue, 1417613151, Tehran, Iran.
Fatemeh AtoofDepartment of Epidemiology and Biostatistics, Kashan University of Medical Sciences, Kashanan, Iran.
Tehran University of Medical Sciences · IRKashan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis is a neurodegenerative disease characterized by the present of leukocytes in the brain tissue and subsequently the formation of sclerotic plaques. Leukocytes penetration into the blood-brain barrier is related to several factors, such as, the conversion of leukocyte gene expression or plasma characteristics. In this frame, we explore alteration of matrix metalloproteinase-2 (MMP-2), transforming growth factor beta (TGF-β) family, and Claudin-11 (as a main myelin structural protein) in leukocytes and blood plasma of multiple sclerosis patients compared to the normal group. Blood samples were collected from thirteen men affected by MS and fifteen healthy men. Leukocyte gene expression was measured using real-time PCR and plasma parameters were examined by ELISA. The results of this study showed that the gene expression of Claudin-11 was significantly higher in MS group compared with normal. Interestingly, the MMP-2 pattern was similar to Claudin-11 and correlated positively with it. It was observed that, although the expressions of TGF-β1 and TGF-β2 are down-regulated in the leukocytes of subjects with MS, they showed higher levels of these cytokines in blood plasma. The plasma level of TGF-β3 in MS patients was higher than normal and correlated with Claudin-11 concentration. In conclusion, the aberrant pattern of Claudin-11, TGF-βs family, and MMP-2 expression in leukocytes of the MS patients was observed in this study. Moreover, the plasma levels of TGF-βs family increased in the MS group. The findings of this study provide clues for further investigations to assay MS pathogenesis.

Indexed as

AdultBlood-Brain BarrierClaudinsFemaleGene ExpressionHumansLeukocytesMaleMatrix Metalloproteinase 2Middle AgedMultiple SclerosisTransforming Growth Factor betaYoung AdultClaudinsCLDN11 protein, humanMatrix Metalloproteinase 2MMP2 protein, humanTransforming Growth Factor betaClaudin-11Matrix metalloproteinaseMultiple sclerosisTransforming growth factor beta

Identifiers

PMID26768647
PMCPMC11482373
OpenAlexW2271067509

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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.