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Updated: Jan 27, 2026

Establishment and Propagation of Human Retinoblastoma Tumors in Immune Deficient Mice
Published on: August 4, 2011
Long Noncoding RNA LINC00202 Promotes Tumor Progression by Sponging miR-3619-5p in Retinoblastoma
Guigang Yan1, Yi Su2, Zhao Ma2
1Department of Ophthalmology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University.
Abstract:
Retinoblastoma (RB) is the most common intraocular malignancy in childhood, and the prognosis in the advanced RB is poor. It is urgent to find novel therapeutic targets. Long noncoding RNAs (lncRNAs) have critical functions in cancer progression, and lncRNA LINC00202 is found associated with poor prognosis in RB. However, the functions of LINC00202 in RB remain unclear. We employed qRT-PCR and immunoblot to detect the expression levels of mRNAs and proteins, respectively. Cell proliferation was determined by CCK-8 assay and colony formation assay. Transwell assays were applied to evaluate the cell abilities of migration and invasion. Luciferase reporter assay was applied to examine RNA stability, and RNA pulldown assays were used to detect interaction between lncRNA and microRNA (miRNA). LINC00202 expression in RB tissues is higher than that in the paired adjacent normal tissues, which has correlation with poor prognosis in RB. RB cell proliferation, migration and invasion were weakened by LINC00202 depletion, but enhanced by LINC00202 overexpression. MiR-3619-5p was identified to directly bind and mediate LINC00202-promoted RB progression, meanwhile, miR-3619-5p directly regulated expression of an oncongene, RIN1. Moreover, RIN1 knockdown completely blocked miR-3619-5p-enhanced RB progression. In summary, high LINC00202 levels are correlated with poor prognosis in RB, and it promotes RB progression by sponging miR-3619-5p and therefore up-regulating RIN1 expression.Key words: LINC00202, miR-3619-5p, retinoblastoma, progression, RIN1.
Insights
High levels of LINC00202 long noncoding RNA correlate with poor prognosis in retinoblastoma (RB). LINC00202 promotes RB progression by interacting with miR-3619-5p, ultimately upregulating RIN1.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Retinoblastoma (RB) is the most common childhood intraocular cancer with a poor prognosis in advanced stages.
- Identifying novel therapeutic targets for RB is crucial.
- Long noncoding RNAs (lncRNAs) play significant roles in cancer progression, with LINC00202 implicated in poor RB prognosis.
Purpose of the Study:
- To investigate the functional role of lncRNA LINC00202 in retinoblastoma (RB) progression.
- To elucidate the molecular mechanism by which LINC00202 influences RB.
- To identify potential therapeutic targets for RB treatment.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) and immunoblotting were used to assess mRNA and protein expression.
- Cell proliferation, migration, and invasion assays (CCK-8, colony formation, Transwell) were performed.
- Luciferase reporter and RNA pulldown assays were employed to study RNA interactions and stability.
Main Results:
- LINC00202 expression was significantly higher in RB tissues compared to adjacent normal tissues and correlated with poor prognosis.
- LINC00202 depletion inhibited RB cell proliferation, migration, and invasion, while overexpression enhanced these processes.
- LINC00202 was found to sponge miR-3619-5p, which in turn regulated the expression of the oncogene RIN1. RIN1 knockdown abrogated the pro-tumorigenic effects of miR-3619-5p.
Conclusions:
- Elevated LINC00202 levels are associated with poor retinoblastoma prognosis.
- LINC00202 promotes RB progression by sponging miR-3619-5p, leading to increased RIN1 expression.
- The LINC00202/miR-3619-5p/RIN1 axis represents a potential therapeutic strategy for retinoblastoma.
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