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Updated: Jan 25, 2026

Reconstruct Human Retinoblastoma In Vitro
Published on: October 11, 2022
FEZF1-AS1 functions as an oncogenic lncRNA in retinoblastoma
Lian-Jiao Quan1, Wen-Jun Wang2,3,4
1Department of Ophthalmology, Qingyang People's Hospital, Qingyan, Gansu 745000, China.
Abstract:
Long non-coding RNA (lncRNA) FEZF1 antisense RNA 1 (FEZF1-AS1) has been shown to be up-regulated in tumor tissues and cells, and exerts oncogenic effects on various types of malignancies. However, the expression and function of FEZF1-AS1 was still fully unclear in retinoblastoma. The purpose of our study was to investigate the expression and clinical value of FEZF1-AS1 in retinoblastoma patients, and explore the effect of FEZF1-AS1 on retinoblastoma cell proliferation, migration and invasion. In our results, levels of FEZF1-AS1 expression were elevated in retinoblastoma tissue specimens and cell lines compared with adjacent normal retina tissue specimens and human retinal pigment epithelial cell line, respectively. The correlation analysis indicated that high FEZF1-AS1 expression was significantly correlated with present choroidal invasion and optic nerve invasion. Survival analysis suggested that retinoblastoma patients in high FEZF1-AS1 expression group had obviously short disease-free survival (DFS) compared with retinoblastoma patients in low FEZF1-AS1 expression group, and high FEZF1-AS1 expression was an independent unfavorable prognostic factor for DFS in retinoblastoma patients. Loss-of-function study indicated silencing FEZF1-AS1 expression inhibited retinoblastoma cell proliferation, invasion and migration. In conclusion, FEZF1-AS1 functions as an oncogenic lncRNA in retinoblastoma.
Insights
Long non-coding RNA FEZF1 antisense RNA 1 (FEZF1-AS1) is elevated in retinoblastoma, correlating with advanced disease and poor survival. Silencing FEZF1-AS1 inhibits tumor cell growth and spread, identifying it as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Ophthalmology
Background:
- Long non-coding RNA (lncRNA) FEZF1 antisense RNA 1 (FEZF1-AS1) is implicated as an oncogene in various cancers.
- The role of FEZF1-AS1 in retinoblastoma, a rare eye cancer, remains largely uncharacterized.
Purpose of the Study:
- To investigate the expression patterns of FEZF1-AS1 in retinoblastoma.
- To evaluate the clinical significance of FEZF1-AS1 expression in retinoblastoma patients.
- To explore the functional role of FEZF1-AS1 in retinoblastoma cell behavior.
Main Methods:
- Quantitative real-time PCR was used to measure FEZF1-AS1 expression levels in tumor and normal tissues/cell lines.
- Correlation analyses were performed to associate FEZF1-AS1 expression with clinical parameters.
- Survival analysis (Kaplan-Meier) was conducted to assess the prognostic value of FEZF1-AS1.
- In vitro loss-of-function experiments (siRNA-mediated silencing) were employed to study FEZF1-AS1's effects on cell proliferation, migration, and invasion.
Main Results:
- FEZF1-AS1 expression was significantly upregulated in retinoblastoma tissues and cell lines compared to controls.
- High FEZF1-AS1 expression correlated significantly with choroidal and optic nerve invasion.
- Elevated FEZF1-AS1 levels were associated with shorter disease-free survival (DFS) and identified as an independent unfavorable prognostic factor.
- Silencing FEZF1-AS1 suppressed retinoblastoma cell proliferation, migration, and invasion.
Conclusions:
- FEZF1-AS1 is overexpressed in retinoblastoma and serves as a potential biomarker for disease progression and prognosis.
- FEZF1-AS1 promotes retinoblastoma cell proliferation, migration, and invasion, acting as an oncogenic lncRNA.
- Targeting FEZF1-AS1 may offer a novel therapeutic strategy for retinoblastoma.
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