Evidence map›Paper›PMID 25810883›Full record

ArticleIranian journal of basic medical sciences2015

MicroRNAs that target RGS5.

Amir Banaei-Esfahani, Hamidreza Moazzeni, Pooya Naseri Nosar, Sadaf Amin, Ehsan Arefian, Masoud Soleimani, Shahin Yazdani, Elahe Elahi

Abstract read
In one paragraph

Article in Iranian journal of basic medical sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. MiR-7 in Cancer Development.Biomedicines · 2021
    Review
  4. Article
  5. Review
  6. Article
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

8 authors at 4 institutions in 1 country.

Amir Banaei-EsfahaniDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Hamidreza MoazzeniDepartment of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Pooya Naseri NosarDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Sadaf AminDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Ehsan ArefianSchool of Biology, College of Science, University of Tehran, Tehran, Iran.
Masoud SoleimaniStem Cell Technology Research Center, Tehran, Iran.
Shahin YazdaniOphthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Elahe ElahiDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran ; School of Biology, College of Science, University of Tehran, Tehran, Iran.
University of Tehran · IRShahid Beheshti University of Medical Sciences · IRStem Cell Technology Research Center · IRTarbiat Modares University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAn earlier meta-analysis on gene expression data derived from four microarray, two cDNA library, and one SAGE experiment had identified RGS5 as one of only ten non-housekeeping genes that were reported to be expressed in human trabecular meshwork (TM) cells by all studies. RGS5 encodes regulator of G-protein signaling-5. The TM tissue is the route of aqueous fluid outflow, and is relevant to the pathology of glaucoma. MicroRNAs constitute the most recently identified components of the cellular machinery for gene regulation in eukaryotic cells. Given our long standing interest in glaucoma, we aimed to identify miRNAs that may target RGS5. MATERIALS AND

methodsEight miRNAs were selected for study using bioinformatics tools and available data on miRNAs expressed in the eye. Their effects were assessed using the dual luciferase assay. 3'-UTR segments of RGS5 mRNA were cloned downstream of a luciferase coding gene in psiCHECK2 vectors, and these were co-transfected with each of the miRNAs into HEK293 cells.

resultsThe outcomes evidenced that one or more of the segments are in fact targeted by miR-7, miR-9, miR-96, miR-23a, miR-23b, miR-204, and miR-211. Down regulations by the miRNAs were statistically significant. The effect of miR-204 is considered particularly important as this miRNA is well known to regulate eye development and to affect multiple ocular functions.

conclusionOur results justify further studies on regulation of RGS5 expression and RGS5 downstream functions by these miRNAs.

Indexed as

miR-204miR-211miR-23amiR-23bmiR-7miR-9miR-96RGS5

Identifiers

PMID25810883
PMCPMC4366720
OpenAlexW1579610602

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.