Evidence map›Paper›PMID 21241758›Full record

ReviewAdvanced drug delivery reviews2011

miRNA and vascular cell movement.

Junming Yue

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2011. 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
1.0field-weighted citation impact, top 22% 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, 34 citations in OpenAlex.

  1. Review
  2. Role of miRNAs in vascular development.Non-coding RNA research · 2023
    Review
  3. MicroRNAs as therapeutic targets in breast cancer metastasis.Drug delivery and translational research · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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

1 author at 1 institution in 1 country.

Junming YueDepartment of Physiology and Cancer Research Institute, University of Tennessee Health Science Center, TN 38163, USA. jyue@uthsc.edu
University of Tennessee Health Science Center · US

Funding

Transgenic rat overexpressing miR-21 in vascular smooth muscle cells:functional iR21HL095957 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI YUE, JUNMING · 2010 to 2011
$421k
Transgenic rat overexpressing miR-15/16 cluster:functional implications in develoR03HD061420 · NICHD · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI YUE, JUNMING · 2009 to 2010
$148k
NHLBI NIH HHS HL095957NHLBI NIH HHS R21 HL095957NICHD NIH HHS HD061420NICHD NIH HHS R03 HD061420
6 · The paper itself

Abstract

miRNAs are a new class of endogenous small RNAs that negatively regulate gene expression at the posttranscriptional level. Accumulating experimental evidence shows that miRNAs regulate cellular apoptosis, proliferation, differentiation, and migration. Dysregulation of miRNA expression leads to various human diseases including cancer and cardiovascular disease. miRNA maturation is regulated at multiple steps by different mechanisms, including miRNA editing, hairpin loop binding, self-regulation, and cross-talk with other signaling pathways. Vascular cell movement plays a pivotal role in the development of various cancers and cardiovascular diseases. miRNAs have been found to regulate vascular cell movement. Presently the chemically synthesized antagomir and miRNA mimics have been widely used in investigating the biological functions of miRNA genes. The viral vectors, including adenoviral, lentiviral, and adeno-associated viral vectors, have been used to efficiently overexpress or knockdown miRNAs in vitro and in vivo. Therefore, targeting vascular cell movement using miRNA-based drug or gene therapy would provide a novel therapeutic approach in the treatment of cancers and vascular diseases.

Indexed as

AnimalsCardiovascular DiseasesCell MovementDrug Delivery SystemsGene Expression RegulationGenetic TherapyGenetic VectorsHumansMicroRNAsNeoplasmsMicroRNAs

Identifiers

PMID21241758
PMCPMC3129380
OpenAlexW2010383142

What OpenQuestion holds

Textmetadata
LicenceTDM
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.