Evidence map›Paper›PMID 29178246›Full record

ArticleBritish journal of pharmacology2018

Effects of the antagomiRs 15b and 200b on the altered healing pattern of diabetic mice.

Gabriele Pizzino, Natasha Irrera, Federica Galfo, Giovanni Pallio, Federica Mannino, Angelica D'amore, Enrica Pellegrino, Antonio Ieni, Giuseppina T Russo, Marco Calapai and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
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  4. Role of exosome-derived miRNAs in diabetic wound angiogenesis.Molecular and cellular biochemistry · 2024
    Review
  5. Article
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  8. Article
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  11. Beyond the Code: Noncoding RNAs in Skin Wound Healing.Cold Spring Harbor perspectives in biology · 2022
    Article
  12. Review
  13. Article
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  15. 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

13 authors at 1 institution in 1 country.

Gabriele PizzinoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Natasha IrreraDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Federica GalfoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Giovanni PallioDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Federica ManninoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Angelica D'amoreDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Enrica PellegrinoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Antonio IeniDepartment of Human Pathology, University of Messina, Messina, Italy.
Giuseppina T RussoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Marco CalapaiDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Domenica AltavillaDepartment of Biomedical Sciences, Dentistry and Morphological and Functional Images, University of Messina, Messina, Italy.
Francesco SquadritoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.
Alessandra BittoDepartment of Clinical and Experimental Medicine, Section of Pharmacology, Medical School, University of Messina, Messina, Italy.ORCID 0000-0001-9300-7532
University of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeDiabetic patients with non-healing ulcers have a reduced expression of VEGF. Genetically diabetic mice have an altered expression pattern of VEGF and its receptor, VEGF receptor 2 (VEGFR-2). In diabetic wounds, the microRNAs, miR15b and miR200b, which respectively inhibit VEGF and VEGF-R2 mRNAs, are up-regulated, further affecting the impaired angiogenesis. We investigated whether anti-miRs directed toward miR15b and miR200b could improve wound repair in genetically diabetic mice. EXPERIMENTAL APPROACH: Skin wounds were produced on the backs of female diabetic mice. The anti-miRs (antimiR15b, antimiR200b or antimiR15b/200b) at 10 mg·kg KEY

resultsmRNA expression of VEGF, VEGFR-2, angiopoietin-1 and its receptor TEK were evaluated after 7 and 14 days. Protein levels of VEGF and transglutaminase II were measured at day 7, while VEGFR-2 and Angiopoietin-1 were measured at day 14. Histological features and the time to achieve a complete wound closure were also examined. Treatment with the anti-miRs improved the analysed parameters and the co-treatment resulted the most effective. CONCLUSION AND IMPLICATIONS: The results suggest that the inhibition of miR15b and miR200b may have a potential application in diabetes-related wound disorders.

Indexed as

AnimalsAntagomirsDiabetes Mellitus, ExperimentalFemaleMiceMice, Inbred C57BLMice, TransgenicMicroRNAsWound HealingAntagomirsMicroRNAsMirn15 microRNA, mouseMirn200 microRNA, mouse

Identifiers

PMID29178246
PMCPMC5786458
OpenAlexW2769649508

What OpenQuestion holds

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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.