1. RETRACTED ARTICLE: Silence of lncRNA ANRIL represses cell growth and promotes apoptosis in retinoblastoma cells through regulating miR-99a and c-Myc
- Author
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Baojun Wang, Yanfan Ren, Qiuli Wang, Yutong Han, Xinxia Zhang, Junxi Hu, and Xiaomin Wang
- Subjects
medicine.diagnostic_test ,Retinoblastoma ,Cell growth ,Chemistry ,Biomedical Engineering ,Pharmaceutical Science ,Medicine (miscellaneous) ,02 engineering and technology ,General Medicine ,Transfection ,021001 nanoscience & nanotechnology ,medicine.disease ,eye diseases ,Flow cytometry ,03 medical and health sciences ,0302 clinical medicine ,Apoptosis ,030220 oncology & carcinogenesis ,medicine ,Cancer research ,Viability assay ,0210 nano-technology ,Protein kinase B ,PI3K/AKT/mTOR pathway ,Biotechnology - Abstract
Retinoblastoma is a rare cancer of the immature retina. This study designed to see the function of the lncRNA ANRIL in retinoblastoma Y79 cells. ANRIL, miR-99a and c-Myc expression in Y79 cells was altered by transfection and then trypan blue, transwell assay and flow cytometry were carried out to evaluate the changes of cell phenotype. The connection between ANRIL, miR-99a and c-Myc was measured by luciferase reporter assay and RNA immunoprecipitation analysis. As a result, ANRIL expression was highly expressed in human retinoblastoma tissue as relative to the adjacent noncancerous tissues. ANRIL suppression inhibited Y79 cells viability, migration, invasion, while promoted apoptosis. ANRIL negatively regulated miR-99a by binding to miR-99a. Silence of miR-99a reversed the ANRIL-knockdown effects on Y79 cells. miR-99a overexpression suppressed Y79 cell viability, migration, invasion, and enhanced apoptosis through downregulating c-Myc. Meanwhile, we found that miR-99a inhibited JAK/STAT and PI3K/AKT pathways. To conclude, it seems that ANRIL suppression inhibits cell growth and metastasis in retinoblastoma Y79 cells by regulating miR-99a and c-Myc.
- Published
- 2019
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