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MiR-372-3p inhibits the growth and metastasis of osteosarcoma cells by targeting FXYD6.
Xu, S-Y; Xu, P-F; Gao, T-T.
Afiliação
  • Xu SY; Department of Orthopaedics, Shanghai Eighth People's Hospital, Shanghai, China. gtt1924g@163.com.
Eur Rev Med Pharmacol Sci ; 22(1): 62-69, 2018 01.
Article em En | MEDLINE | ID: mdl-29364472
ABSTRACT

OBJECTIVE:

Growing evidence has suggested that dysregulation of miR-372-3p may contribute to tumor development and progression in various tumors. However, the function of miR-372-3p in osteosarcoma has not been investigated. In the present study, we aimed to study the effects of miR-372-3p on osteosarcoma cell proliferation and metastasis and its regulation on FXYD6. MATERIALS AND

METHODS:

The expression levels of miR-372-3p and FXYD6 mRNA were quantified by RT-PCR in human osteosarcoma cell lines and tissues. The effects of miR-372-3p up-regulation on osteosarcoma cell proliferation and metastasis were assessed by MTT, wound healing assay and transwell assay. Finally, the potential regulatory effect of miR-372-3p on FXYD6 expression was confirmed.

RESULTS:

Our data showed that miR-372-3p was downregulated in osteosarcoma tissues compared with matched normal tissues, and the expression level of miR-372-3p was significantly lower in osteosarcoma cell lines in comparison with the normal human osteoblastic cell line. Transfection with the miR-372-3p mimic enhanced the osteosarcoma proliferation and metastasis. In vivo assay indicated that forced expression of miR-372-3p significantly suppressed tumor growth. Then, Bioinformatics prediction and experimental validation results confirmed that the function of miR-372-3p was achieved by targeting FXYD6 expression.

CONCLUSIONS:

Our findings revealed that miR-372-3p served as a tumor suppressor gene by targeting FXYD6 in osteosarcoma. Thus, miR-372-3 might be a potential therapeutic method for osteosarcoma.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Osteossarcoma / MicroRNAs / Canais Iônicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Eur Rev Med Pharmacol Sci Assunto da revista: FARMACOLOGIA / TOXICOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China País de publicação: IT / ITALIA / ITALY / ITÁLIA

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Osteossarcoma / MicroRNAs / Canais Iônicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Eur Rev Med Pharmacol Sci Assunto da revista: FARMACOLOGIA / TOXICOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China País de publicação: IT / ITALIA / ITALY / ITÁLIA