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人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响

BACKGROUND AND OBJECTIVE: The abnormal expression of human long chain non encoding RNA gene is related to many kinds of tumors. The aim of this study is to investigate the expression of long non-coding RNA maternally expressed gene 3 (SPRY4-IT1) in lung cancer (A549) cells, and to observe the effect...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000226/
https://www.ncbi.nlm.nih.gov/pubmed/26302345
http://dx.doi.org/10.3779/j.issn.1009-3419.2015.08.07
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collection PubMed
description BACKGROUND AND OBJECTIVE: The abnormal expression of human long chain non encoding RNA gene is related to many kinds of tumors. The aim of this study is to investigate the expression of long non-coding RNA maternally expressed gene 3 (SPRY4-IT1) in lung cancer (A549) cells, and to observe the effect of SPRY4-IT1 on the invasion and migration of A549 cells. METHODS: The levels of SPRY4-IT1 in A549 was detected by real-time PCR. The effects of SPRY4-IT1 on the invasion and migration of A549 cell were analyzed by MTT and Transwell assay. The expression of matrix metalloproteinase (MMP) family proteins was determined by Western blot. RESULTS: The invasion and migration of A549 cells were increased after SPRY4-IT1 over-expression. The cell spaces were narrower after SPRY4-IT1 over-expression in the wound healing assay. Transwell assays showed that the numbers of transmembrane A549 cells were higher in SPRY4-IT1 over-expression group than control group (P < 0.05). Meanwhile, over-expression of SPRY4-IT1 reduced the expression of matrix metalloproteinase (MMP)-2 and MMP-9. CONCLUSION: Over-expression of SPRY4-IT1 enhanced the invasion and migration of A549 cells. MMP-2 and MMP-9 might play an important role in this regulation.
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spelling pubmed-60002262018-07-06 人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响 Zhongguo Fei Ai Za Zhi 基础研究 BACKGROUND AND OBJECTIVE: The abnormal expression of human long chain non encoding RNA gene is related to many kinds of tumors. The aim of this study is to investigate the expression of long non-coding RNA maternally expressed gene 3 (SPRY4-IT1) in lung cancer (A549) cells, and to observe the effect of SPRY4-IT1 on the invasion and migration of A549 cells. METHODS: The levels of SPRY4-IT1 in A549 was detected by real-time PCR. The effects of SPRY4-IT1 on the invasion and migration of A549 cell were analyzed by MTT and Transwell assay. The expression of matrix metalloproteinase (MMP) family proteins was determined by Western blot. RESULTS: The invasion and migration of A549 cells were increased after SPRY4-IT1 over-expression. The cell spaces were narrower after SPRY4-IT1 over-expression in the wound healing assay. Transwell assays showed that the numbers of transmembrane A549 cells were higher in SPRY4-IT1 over-expression group than control group (P < 0.05). Meanwhile, over-expression of SPRY4-IT1 reduced the expression of matrix metalloproteinase (MMP)-2 and MMP-9. CONCLUSION: Over-expression of SPRY4-IT1 enhanced the invasion and migration of A549 cells. MMP-2 and MMP-9 might play an important role in this regulation. 中国肺癌杂志编辑部 2015-08-20 /pmc/articles/PMC6000226/ /pubmed/26302345 http://dx.doi.org/10.3779/j.issn.1009-3419.2015.08.07 Text en 版权所有©《中国肺癌杂志》编辑部2015 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 基础研究
人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响
title 人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响
title_full 人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响
title_fullStr 人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响
title_full_unstemmed 人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响
title_short 人长链非编码RNA基因SPRY4-ITl对肺癌细胞A549侵袭和迁移能力的影响
title_sort 人长链非编码rna基因spry4-itl对肺癌细胞a549侵袭和迁移能力的影响
topic 基础研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000226/
https://www.ncbi.nlm.nih.gov/pubmed/26302345
http://dx.doi.org/10.3779/j.issn.1009-3419.2015.08.07
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