Evidence map›Paper›PMID 19940135›Full record

ArticleThe Journal of biological chemistry2010

Targeting of integrin beta1 and kinesin 2alpha by microRNA 183.

Guorong Li, Coralia Luna, Jianming Qiu, David L Epstein, Pedro Gonzalez

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

64 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. 5'isomiR-183-5p|+2 elicits tumor suppressor activity in a negative feedback loop with E2F1.Journal of experimental & clinical cancer research : CR · 2022
    Article
  7. The role of microRNAs in glaucoma.Experimental eye research · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. MicroRNA-183 in Cancer Progression.Journal of Cancer · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Guorong LiDepartment of Ophthalmology, Duke University, Durham, North Carolina 27710, USA.
Coralia Luna
Jianming Qiu
David L Epstein
Pedro Gonzalez
Duke University · US

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
METABOLISM OF THE TRABECULAR MESHWORKR01EY001894 · NEI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI EPSTEIN, DAVID L · 1985 to 2011
$4.2M
Cellular Senescence and GlaucomaR01EY016228 · NEI · DUKE UNIVERSITY · PI GONZALEZ, PEDRO · 2005 to 2011
$2.2M
Oxidative Stress and Lysosomal Function in the Outflow PathwayR21EY019137 · NEI · DUKE UNIVERSITY · PI LITON, PALOMA · 2008 to 2009
$545k
NEI NIH HHS EY016228NEI NIH HHS EY01894NEI NIH HHS EY019137NEI NIH HHS EY05722NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY001894NEI NIH HHS R01 EY016228NEI NIH HHS R21 EY019137
6 · The paper itself

Abstract

MicroRNA 183 (miR-183) has been reported to inhibit tumor invasiveness and is believed to be involved in the development and function of ciliated neurosensory organs. We have recently found that expression of miR-183 increased after the induction of cellular senescence by exposure to H(2)O(2). To gain insight into the biological roles of miR-183 we investigated two potential novel targets: integrin beta1 (ITGB1) and kinesin 2alpha (KIF2A). miR-183 significantly decreased the expression of ITGB1 and KIF2A measured by Western blot. Targeting of the 3'-untranslated region (3'-UTR) of ITGB1 and KIF2A by miR-183 was confirmed by luciferase assay. Transfection with miR-183 led to a significant decrease in cell invasion and migration capacities of HeLa cells that could be rescued by expression of ITGB1 lacking the 3'-UTR. Although miR-183 had no effects on cell adhesion in HeLa cells, it significantly decreased adhesion to laminin, gelatin, and collagen type I in normal human diploid fibroblasts and human trabecular meshwork cells. These effects were also rescued by expression of ITGB1 lacking the 3'-UTR. Targeting of KIF2A by miR-183 resulted in some increase in the formation of cells with monopolar spindles in HeLa cells but not in human diploid fibroblast or human trabecular meshwork cells. The regulation of ITGB1 expression by miR-183 provides a new mechanism for the anti-metastatic role of miR-183 and suggests that this miRNA could influence the development and function in neurosensory organs, and contribute to functional alterations associated with cellular senescence in human diploid fibroblasts and human trabecular meshwork cells.

Indexed as

3' Untranslated RegionsCell AdhesionCell MovementFibroblastsGene Expression RegulationHeLa CellsHumansIntegrin beta1KinesinsMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisTrabecular Meshwork3' Untranslated RegionsIntegrin beta1KIF2A protein, humanKinesinsMicroRNAsMIRN183 microRNA, human

Identifiers

PMID19940135
PMCPMC2820774
OpenAlexW1520622777

What OpenQuestion holds

Textmetadata
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.