Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression

AIM:To investigate the level of miR-218 in human retinoblastoma(RB)and its effect on the potential mechanism of tumorgenesis. <p>METHODS:Real-time PCR was applied to detect the expression of miR-218 in human RB and the corresponding tumor-adjacent tissues to analyze the relation between miR-21...

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Main Authors: Lin-Sheng Yang, Li-Lun Wang, Qing-Wei Du
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2015-12-01
Series:Guoji Yanke Zazhi
Subjects:
Online Access:http://ies.ijo.cn/cn_publish/2015/12/201512005.pdf
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spelling doaj-825b36f280684120a9419c3d29f027702020-11-24T23:06:39ZengPress of International Journal of Ophthalmology (IJO PRESS)Guoji Yanke Zazhi1672-51231672-51232015-12-0115122045204810.3980/j.issn.1672-5123.2015.12.05Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expressionLin-Sheng Yang0Li-Lun Wang1Qing-Wei Du2Department of Ophthalmology,Yan'an University Affiliated Hospital, Yan'an 716000, Shaanxi Province, ChinaDepartment of Ophthalmology,Yan'an University Affiliated Hospital, Yan'an 716000, Shaanxi Province, ChinaDepartment of Ophthalmology,Yan'an University Affiliated Hospital, Yan'an 716000, Shaanxi Province, ChinaAIM:To investigate the level of miR-218 in human retinoblastoma(RB)and its effect on the potential mechanism of tumorgenesis. <p>METHODS:Real-time PCR was applied to detect the expression of miR-218 in human RB and the corresponding tumor-adjacent tissues to analyze the relation between miR-218 and clinic pathology characteristics. The artificial miR-218 was transiently transfected into human Y79 cells in <i>vitro</i>. The proliferation and apoptosis of the cells were detected by MTT assay and flow cytometry, respectively. The expression level of Bmi-1 mRNA and protein were determined by RT-PCR and Western blot. <p>RESULTS:The expression level of miR-218 in RB tissues was significantly lower than that in the adjacent tissues, and it was associated with optic nerve infiltration and differentiated degree. Over-expressed miR-218 in Y79 cells suppressed cell proliferation and promoted cell apoptosis, and down-regulated mRNA and protein expressions of Bmi-1. <p>CONCLUSION:The expression of miR-218 in RB tissues is significantly lower than that in tumor-adjacent tissues.MiR-218 could inhibit RB cell proliferation and induce apoptosis by down-regulating the expression of Bmi-1.http://ies.ijo.cn/cn_publish/2015/12/201512005.pdfmiR-218retinoblastomaproliferationapoptosisBmi-1
collection DOAJ
language English
format Article
sources DOAJ
author Lin-Sheng Yang
Li-Lun Wang
Qing-Wei Du
spellingShingle Lin-Sheng Yang
Li-Lun Wang
Qing-Wei Du
Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression
Guoji Yanke Zazhi
miR-218
retinoblastoma
proliferation
apoptosis
Bmi-1
author_facet Lin-Sheng Yang
Li-Lun Wang
Qing-Wei Du
author_sort Lin-Sheng Yang
title Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression
title_short Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression
title_full Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression
title_fullStr Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression
title_full_unstemmed Growth inhibition of human retinoblastoma by miR-218 <i>via</i> down-regulation of Bmi-1 expression
title_sort growth inhibition of human retinoblastoma by mir-218 <i>via</i> down-regulation of bmi-1 expression
publisher Press of International Journal of Ophthalmology (IJO PRESS)
series Guoji Yanke Zazhi
issn 1672-5123
1672-5123
publishDate 2015-12-01
description AIM:To investigate the level of miR-218 in human retinoblastoma(RB)and its effect on the potential mechanism of tumorgenesis. <p>METHODS:Real-time PCR was applied to detect the expression of miR-218 in human RB and the corresponding tumor-adjacent tissues to analyze the relation between miR-218 and clinic pathology characteristics. The artificial miR-218 was transiently transfected into human Y79 cells in <i>vitro</i>. The proliferation and apoptosis of the cells were detected by MTT assay and flow cytometry, respectively. The expression level of Bmi-1 mRNA and protein were determined by RT-PCR and Western blot. <p>RESULTS:The expression level of miR-218 in RB tissues was significantly lower than that in the adjacent tissues, and it was associated with optic nerve infiltration and differentiated degree. Over-expressed miR-218 in Y79 cells suppressed cell proliferation and promoted cell apoptosis, and down-regulated mRNA and protein expressions of Bmi-1. <p>CONCLUSION:The expression of miR-218 in RB tissues is significantly lower than that in tumor-adjacent tissues.MiR-218 could inhibit RB cell proliferation and induce apoptosis by down-regulating the expression of Bmi-1.
topic miR-218
retinoblastoma
proliferation
apoptosis
Bmi-1
url http://ies.ijo.cn/cn_publish/2015/12/201512005.pdf
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