Evidence map›Paper›PMID 29342922›Full record

ReviewInternational journal of molecular sciences2018

Can EGCG Alleviate Symptoms of Down Syndrome by Altering Proteolytic Activity?

Marzena Wyganowska-Świątkowska, Maja Matthews-Kozanecka, Teresa Matthews-Brzozowska, Ewa Skrzypczak-Jankun, Jerzy Jankun

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  4. [Whole-transcriptome sequencing analysis of placental differential miRNA expression profile in Down syndrome].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    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

5 authors at 2 institutions in 2 countries.

Marzena Wyganowska-ŚwiątkowskaDepartment of Dental Surgery and Periodontology, Poznań University of Medical Sciences, Bukowska 70, 60-812 Poznań, Poland. marzena.wyganowska@periona.pl.
Maja Matthews-KozaneckaDepartment of Social Sciences, Poznań University of Medical Sciences, Fredry 10, 61-710 Poznań, Poland. pszczolka-maja@o2.pl.
Teresa Matthews-BrzozowskaThe Chair and Clinic of Maxillofacial Orthopaedics and Orthodontics, Poznań University of Medical Sciences, Bukowska 70, 60-812 Poznań, Poland. teresamatbrzo@gmail.com.
Ewa Skrzypczak-JankunUrology Research Center, Department of Urology, The University of Toledo-Health Science Campus, 3000 Arlington Ave, Toledo, OH 43614, USA. Ewa.Skrzypczak-Jankun@utoledo.edu.
Jerzy JankunUrology Research Center, Department of Urology, The University of Toledo-Health Science Campus, 3000 Arlington Ave, Toledo, OH 43614, USA. Jerzy.Jankun@utoledo.edu.
Poznan University of Medical Sciences · PLUniversity of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Down syndrome (DS), also known as "trisomy 21", is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. Silencing these extra genes is beyond existing technology and seems to be impractical. A number of pharmacologic options have been proposed to change the quality of life and lifespan of individuals with DS. It was reported that treatment with epigallocatechin gallate (EGCG) improves cognitive performance in animal models and in humans, suggesting that EGCG may alleviate symptoms of DS. Traditionally, EGCG has been associated with the ability to reduce dual specificity tyrosine phosphorylation regulated kinase 1A activity, which is overexpressed in trisomy 21. Based on the data available in the literature, we propose an additional way in which EGCG might affect trisomy 21-namely by modifying the proteolytic activity of the enzymes involved. It is known that, in Down syndrome, the nerve growth factor (NGF) metabolic pathway is altered: first by downregulating tissue plasminogen activator (tPA) that activates plasminogen to plasmin, an enzyme converting proNGF to mature NGF; secondly, overexpression of metalloproteinase 9 (MMP-9) further degrades NGF, lowering the amount of mature NGF. EGCG inhibits MMP-9, thus protecting NGF. Urokinase (uPA) and tPA are activators of plasminogen, and uPA is inhibited by EGCG, but regardless of their structural similarity tPA is not inhibited. In this review, we describe mechanisms of proteolytic enzymes (MMP-9 and plasminogen activation system), their role in Down syndrome, their inhibition by EGCG, possible degradation of this polyphenol and the ability of EGCG and its degradation products to cross the blood-brain barrier. We conclude that known data accumulated so far provide promising evidence of MMP-9 inhibition by EGCG in the brain, which could slow down the abnormal degradation of NGF.

Indexed as

AnimalsBiomarkersCatechinDown SyndromeHumansMatrix Metalloproteinase InhibitorsMetalloendopeptidasesMethylationProteolysisSignal TransductionTissue Plasminogen ActivatorBiomarkersCatechinepigallocatechin gallateMatrix Metalloproteinase InhibitorsMetalloendopeptidasesTissue Plasminogen ActivatorDown syndromeepigallocatechin gallatemetalloproteinase 9plasminogen activator system

Identifiers

PMID29342922
PMCPMC5796196
OpenAlexW2783476402

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.