Evidence map›Paper›PMID 29204818›Full record

ArticleMolecular and cellular biochemistry2018

Mir-513a-3p contributes to the controlling of cellular migration processes in the A549 lung tumor cells by modulating integrin β-8 expression.

Marina Bonfogo da Silveira, Kelvin Furtado Lima, Andrea Renata da Silva, Robson Augusto Souza Dos Santos, Karen C M Moraes

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2018. 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
0.7field-weighted citation impact, top 33% 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, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The circular RNA circCRIM1 inhibits osteosarcoma progression through sponging miR-513.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
    Article
  5. SARS-CoV-2 may regulate cellular responses through depletion of specific host miRNAs.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  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

5 authors at 3 institutions in 1 country.

Marina Bonfogo da SilveiraLaboratório de Biologia Molecular, Departamento de Biologia, Instituto de Biociências, Universidade Estadual Paulista "Júlio de Mesquita Filho", Rio Claro, São Paulo, 13506-900, Brazil.
Kelvin Furtado LimaInstituto de Química, Universidade Estadual Paulista "Júlio de Mesquita Filho", Araraquara, São Paulo, Brazil.
Andrea Renata da SilvaNúcleo de Pesquisa em Biologia, Universidade Federal de Ouro Preto, Ouro Preto, Minas Gerais, Brazil.
Robson Augusto Souza Dos SantosLaboratório de Fisiologia, Departmento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Karen C M MoraesLaboratório de Biologia Molecular, Departamento de Biologia, Instituto de Biociências, Universidade Estadual Paulista "Júlio de Mesquita Filho", Rio Claro, São Paulo, 13506-900, Brazil. Karenmor@rc.unesp.com.
Universidade Estadual Paulista (Unesp) · BRUniversidade Federal de Minas Gerais · BRUniversidade Federal de Ouro Preto · BR

Funding

CNPq # 475586/2012-3FAPESP 2014/21645-2
6 · The paper itself

Abstract

Lung tumors are a frequent type of cancer in humans and a leading cause of death, and the late diagnostic contributes to high mortality rates. New therapeutic strategies are needed, and the heptapeptide angiotensin-(1-7) [ang-(1-7)] demonstrated the ability to control cancer growth rates and migration in vitro and in vivo. However, the possible use of the heptapeptide in clinical trials demands deeper analyses to elucidate molecular mechanisms of its effect in the target cells. In this study, we investigated relevant elements that control pro-inflammatory environment and cellular migration, focusing in the post-transcription mechanism using lung tumor cell line. In our cellular model, the microRNA-513a-3p was identified as a novel element targeting ITG-β8, thereby controlling the protein level and its molecular function in the controlling of migration and pro-inflammatory environment. These findings provide useful information for future studies, using miR-513a-3p as an innovative molecular tool to control lung tumor cell migration, which will support more effective clinical treatment of the patients with the widely used chemotherapeutic agents, increasing survival rates.

Indexed as

Cell MovementModels, BiologicalA549 CellsHumansIntegrin beta ChainsLung NeoplasmsMicroRNAsNeoplasm ProteinsRNA, Neoplasmintegrin beta8Integrin beta ChainsMicroRNAsMIRN513A1 microRNA, humanNeoplasm ProteinsRNA, NeoplasmCellular migration processesPro-inflammatory environmentSmall non-coding RNAsTumorigenesesVasoactive peptide

Identifiers

PMID29204818
OpenAlexW2773632823

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.