Evidence map›Paper›PMID 32340317›Full record

ArticleInternational journal of molecular sciences2020

A Novel CD147 Inhibitor, SP-8356, Attenuates Pathological Fibrosis in Alkali-Burned Rat Cornea.

Chanmin Joung, Hyojin Noh, Jeein Jung, Hwa Young Song, Hwanse Bae, Kisoo Pahk, Won-Ki Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  6. Consilience and unity in ocular anterior segment research.International journal of ophthalmology · 2024
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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.

Chanmin JoungInstitute for Inflammation Control, Korea University, Seoul 02841, Korea.
Hyojin NohInstitute for Inflammation Control, Korea University, Seoul 02841, Korea.
Jeein JungInstitute for Inflammation Control, Korea University, Seoul 02841, Korea.
Hwa Young SongShinpoong Pharmaceutical Company, Ansan 15610, Korea.
Hwanse BaeInstitute for Inflammation Control, Korea University, Seoul 02841, Korea.
Kisoo PahkInstitute for Inflammation Control, Korea University, Seoul 02841, Korea.ORCID 0000-0003-2971-4202
Won-Ki KimInstitute for Inflammation Control, Korea University, Seoul 02841, Korea.
Korea University · KRShin Poong Pharm (South Korea) · KR

Funding

Ministry of Trade, Industry and Energy 10078367
6 · The paper itself

Abstract

The corneal fibrotic responses to corneal damage often lead to severe corneal opacification thereby resulting in severe visual impairment or even blindness. The persistence of corneal opacity depends heavily on the activity of corneal myofibroblast. Myofibroblasts are opaque and synthesize a disorganized extracellular matrix (ECM) and thus promoting opacification. Cluster of differentiation 147 (CD147), a member of the immunoglobulin superfamily, is known to play important roles in the differentiation process from fibroblast to myofibroblast in damaged cornea and may therefore be an effective target for treatment of corneal opacity. Here, we examined the therapeutic efficacy of novel CD147 inhibiting verbenone derivative SP-8356 ((1S,5R)-4-(3,4-dihydroxy-5-methoxystyryl)-6,6-dimethylbicyclo[3.1.1]hept-3-en-2-one) on corneal fibrosis. Topical SP-8356 significantly reduced corneal haze and fibrosis in the alkali-burned cornea. In detail, SP-8356 inhibited both alpha-smooth muscle actin (α-SMA) expressing myofibroblast and its ECM-related products, such as matrix-metalloproteinase-9 and collagen type III and IV. Similar to SP-8356, topical corticosteroid (prednisolone acetate, PA) also reduced the ECM-related products and opacification. However, prednisolone acetate failed to decrease the population of α-SMA-positive corneal myofibroblast. In conclusion, SP-8356 is capable enough to prevent corneal haze by preventing pathological fibrosis after severe corneal damage. Therefore, SP-8356 could be a potentially promising therapeutic drug for corneal fibrosis.

Indexed as

AlkaliesAnimalsBasiginBicyclic MonoterpenesBiopsyCollagenCorneal InjuriesCytokinesDisease Models, AnimalEye BurnsFibroblastsFibrosisImmunohistochemistryInflammation MediatorsMaleRatsAlkaliesBasiginBicyclic MonoterpenesCollagenCytokinesInflammation MediatorsSP-8356alpha-smooth muscle actincollagen type IIIcorneal alkali burncorneal hazematrix-metalloproteinaseMMP-9myofibroblast

Identifiers

PMID32340317
PMCPMC7215672
OpenAlexW3019603818

What Socratic 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 Socratic graph.