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miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN

The aim of this study is to explain the effects and mechanism of miRNA‐216 in osteosarcoma. We firstly evaluated the PTEN expression in 30 pairs of tumor and adjacent tissues which were from the 30 osteosarcoma patients. In the following cell experiments, we measured the cell proliferation, cell cyc...

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Detalles Bibliográficos
Autores principales: Jiang, Ping, Yang, Xin, Li, Yuanli, Chen, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500758/
https://www.ncbi.nlm.nih.gov/pubmed/32994932
http://dx.doi.org/10.1002/fsn3.1587
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author Jiang, Ping
Yang, Xin
Li, Yuanli
Chen, Juan
author_facet Jiang, Ping
Yang, Xin
Li, Yuanli
Chen, Juan
author_sort Jiang, Ping
collection PubMed
description The aim of this study is to explain the effects and mechanism of miRNA‐216 in osteosarcoma. We firstly evaluated the PTEN expression in 30 pairs of tumor and adjacent tissues which were from the 30 osteosarcoma patients. In the following cell experiments, we measured the cell proliferation, cell cycle, cell invasion, and migration abilities of NC (normal control) group, BL (blank) group, siRNA (miRNA‐216 inhibitor) group, and siRNA+PTEN inhibitor group. Furthermore, we measured the relative protein expression of difference groups by WB to explain the mechanism of miRNA‐216 in osteosarcoma. The PTEN was confirmed the target gene of miRNA‐216 by double luciferase target test. In conclusion, miRNA‐216 was an oncogene in osteosarcoma. miRNA‐216 knockdown had effects to suppress cancer cell proliferation, invasion and migration and improve cell apoptosis by keeping in G1 phase via PTEN.
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spelling pubmed-75007582020-09-28 miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN Jiang, Ping Yang, Xin Li, Yuanli Chen, Juan Food Sci Nutr Original Research The aim of this study is to explain the effects and mechanism of miRNA‐216 in osteosarcoma. We firstly evaluated the PTEN expression in 30 pairs of tumor and adjacent tissues which were from the 30 osteosarcoma patients. In the following cell experiments, we measured the cell proliferation, cell cycle, cell invasion, and migration abilities of NC (normal control) group, BL (blank) group, siRNA (miRNA‐216 inhibitor) group, and siRNA+PTEN inhibitor group. Furthermore, we measured the relative protein expression of difference groups by WB to explain the mechanism of miRNA‐216 in osteosarcoma. The PTEN was confirmed the target gene of miRNA‐216 by double luciferase target test. In conclusion, miRNA‐216 was an oncogene in osteosarcoma. miRNA‐216 knockdown had effects to suppress cancer cell proliferation, invasion and migration and improve cell apoptosis by keeping in G1 phase via PTEN. John Wiley and Sons Inc. 2020-08-09 /pmc/articles/PMC7500758/ /pubmed/32994932 http://dx.doi.org/10.1002/fsn3.1587 Text en © 2020 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Jiang, Ping
Yang, Xin
Li, Yuanli
Chen, Juan
miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN
title miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN
title_full miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN
title_fullStr miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN
title_full_unstemmed miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN
title_short miRNA‐216 knockdown has effects to suppress osteosarcoma via stimulating PTEN
title_sort mirna‐216 knockdown has effects to suppress osteosarcoma via stimulating pten
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500758/
https://www.ncbi.nlm.nih.gov/pubmed/32994932
http://dx.doi.org/10.1002/fsn3.1587
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