Evidence map›Paper›PMID 27078876›Full record

ArticlePloS one2016

Sphingomyelinase D from Loxosceles laeta Venom Induces the Expression of MMP7 in Human Keratinocytes: Contribution to Dermonecrosis.

Mara A Corrêa, Cinthya K Okamoto, Rute M Gonçalves-de-Andrade, Carmen W van den Berg, Denise V Tambourgi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. 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
2.7field-weighted citation impact, top 10% 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, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. PeerJ · 2020
    Article
  9. Tick-Borne Flavivirus Inhibits Sphingomyelinase (Frontiers in cellular and infection microbiology · 2020
    Article
  10. Sphingomyelinases D FromFrontiers in pharmacology · 2020
    Article
  11. Article
  12. Effects of copaiba oil on dermonecrosis induced byThe journal of venomous animals and toxins including tropical diseases · 2019
    Article
  13. Article
  14. Highlights in the knowledge of brown spider toxins.The journal of venomous animals and toxins including tropical diseases · 2017
    Review
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.

Mara A CorrêaImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Cinthya K OkamotoImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Rute M Gonçalves-de-AndradeImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Carmen W van den BergInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Denise V TambourgiImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Instituto Butantan · BRCardiff University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Envenomation by Loxosceles spider is characterized by the development of dermonecrosis. In previous studies, we have demonstrated that increased expression/secretion of matrix metalloproteinases 2 and 9, induced by Loxosceles intermedia venom Class 2 SMases D (the main toxin in the spider venom), contribute to the development of cutaneous loxoscelism. In the present study we show that the more potent venom containing the Class 1 SMase D from Loxosceles laeta, in addition to increasing the expression/secretion of MMP2 and MMP9, also stimulates the expression of MMP7 (Matrilysin-1), which was associated with keratinocyte cell death. Tetracycline, a matrix metalloproteinase inhibitor, prevented cell death and reduced MMPs expression. Considering that L. laeta venom is more potent at inducing dermonecrosis than L. intermedia venom, our results suggest that MMP7 may play an important role in the severity of dermonecrosis induced by L. laeta spider venom SMase D. In addition, the inhibition of MMPs by e.g. tetracyclines may be considered for the treatment of the cutaneous loxoscelism.

Indexed as

AnimalsAnti-Bacterial AgentsApoptosisArthropod ProteinsBlotting, WesternCell LineCell SurvivalDose-Response Relationship, DrugHumansKeratinocytesMatrix Metalloproteinase 2Matrix Metalloproteinase 7Matrix Metalloproteinase 9NecrosisPhosphoric Diester HydrolasesRabbitsAnti-Bacterial AgentsArthropod ProteinsMatrix Metalloproteinase 2Matrix Metalloproteinase 7Matrix Metalloproteinase 9Phosphoric Diester Hydrolasessphingomyelin phosphodiesterase DSpider VenomsTetracycline

Identifiers

PMID27078876
PMCPMC4831769
OpenAlexW2340212795

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.