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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

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

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Author(s):
da Silveira, Marina Bonfogo [1] ; Lima, Kelvin Furtado [2] ; da Silva, Andrea Renata [3] ; Souza dos Santos, Robson Augusto [4] ; Moraes, Karen C. M. [1]
Total Authors: 5
Affiliation:
[1] Univ Estadual Paulista, Inst Biociencias, Dept Biol, Lab Biol Mol, BR-13506900 Sao Paulo - Brazil
[2] Univ Estadual Paulista, Inst Quim, Sao Paulo - Brazil
[3] Univ Fed Ouro Preto, Nucleo Pesquisa Biol, Ouro Preto, MG - Brazil
[4] Univ Fed Minas Gerais, Dept Fisiol & Biofis, Lab Fisiol, Belo Horizonte, MG - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Molecular and Cellular Biochemistry; v. 444, n. 1-2, p. 43-52, JUL 2018.
Web of Science Citations: 1
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-beta 8, 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. (AU)

FAPESP's process: 14/21645-2 - Small non-coding RNAs and their connections with molecules correlated with the adhesion and migration process in human lung cancer
Grantee:Marina Bonfogo da Silveira
Support Opportunities: Scholarships in Brazil - Scientific Initiation
FAPESP's process: 13/21186-5 - Molecular networks regulated by small non-coding RNAs in hepatic fibrosis process and their modulatory effect of the vasoactive peptide angiotensin-(1-7)
Grantee:Karen Cristiane Martinez de Moraes
Support Opportunities: Regular Research Grants