Knockdown of long noncoding RNA 00152 (LINC00152) inhibits human retinoblastoma progression.

Abstract:

Background:A growing body of evidence supports the involvement of long noncoding RNA 00152 (LINC00152) in the progression and metastasis of multiple cancers. However, the exact roles of LINC00152 in the progression of human retinoblastoma (RB) remain unknown. We explored the expression and biological function of human RB. Materials and methods:The expression level of LINC00152 in RB tissues and cells was analyzed using quantitative real-time PCR. The function of LINC00152 was determined using a series of in vitro assays. In vivo, a nude mouse model was established to analyze the function of LINC00152. Gene and protein expressions were detected using quantitative real-time PCR and Western blot assays, respectively. Results:The expression of LINC00152 mRNA was upregulated in RB tissues and cell lines. Knockdown of LINC00152 significantly inhibited cell proliferation, colony formation, migration, and invasion and promoted cell apoptosis and caspase-3 and caspase-8 activities in vitro, as well as suppressing tumorigenesis in vivo. We identified several genes related to proliferation, apoptosis, and invasion including Ki-67, Bcl-2, and MMP-9 that were transcriptionally inactivated by LINC00152. Conclusion:Taken together, these data implicate LINC00152 as a therapeutic target in RB.

journal_name

Onco Targets Ther

journal_title

OncoTargets and therapy

authors

Li S,Wen D,Che S,Cui Z,Sun Y,Ren H,Hao J

doi

10.2147/OTT.S160428

subject

Has Abstract

pub_date

2018-06-06 00:00:00

pages

3215-3223

issn

1178-6930

pii

ott-11-3215

journal_volume

11

pub_type

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