Investigator

Xiaojun Liu

Union Hospital

XLXiaojun Liu
Papers(2)
RETRACTED: Long non‐c…LncRNA TTN‐AS1 acts a…
Institutions(1)
Union Hospital

Papers

RETRACTED: Long non‐coding RNA FEZF1‐AS1 induced progression of ovarian cancer via regulating miR‐130a‐5p/SOX4 axis

Abstract Emerging studies have revealed the critical role of long non‐coding RNAs (lncRNAs) in epithelial ovarian cancer (EOC) development and progression. Till now, the roles and potential mechanisms regarding FEZF1 antisense RNA 1 (FEZF1‐AS1) within ovarian cancer (OC) remain unclear. The objective of this study was to uncover the biological function and the underlying mechanism of LncRNA FEZF1‐AS1 in OC progression. FEZF1‐AS1 expression levels were studied in cell lines and tissues of human ovarian cancer. In vitro studies were performed to evaluate the impact of FEZF1‐AS1 knock‐down on the proliferation, invasion, migration and apoptosis of OC cells. Interactions of FEZF1‐AS1 and its target genes were identified by luciferase reporter assays. Our data showed overexpression of FEZF1‐AS1 in OC cell lines and tissues. Cell migration, proliferation, invasion, wound healing and colony formation were suppressed by silencing of FEZF1‐AS1. In contrast, cell apoptosis was promoted by FEZF1‐AS1 knock‐down in vitro. Furthermore, online bioinformatics analysis and tools suggested that FEZF1‐AS1 directly bound to miR‐130a‐5p and suppressed its expression. Moreover, the inhibitory effects of miR‐130a‐5p on the OC cell growth were reversed by FEZF1‐AS1 overexpression, which was associated with the increase in SOX4 expression. In conclusion, our results revealed that FEZF1‐AS1 promoted the metastasis and proliferation of OC cells by targeting miR‐130a‐5p and its downstream SOX4 expression.

LncRNA TTN‐AS1 acts as sponge for miR‐15b‐5p to regulate FBXW7 expression in ovarian cancer

AbstractEmerging evidence showed that long noncoding RNA (lncRNA) plays crucial roles in regulating various cancer biological behaviors. Titin‐antisense RNA1 (TTN‐AS1) has been reported to have crucial roles in cancers but its role in ovarian cancer remains unknown. The levels of TTN‐AS1, microNRA‐15b‐5p (miR‐15b‐5p), and F‐box and WD repeat domain containing 7 (FBXW7) in ovarian cancer cells were measured by quantitative reverse‐transcription PCR. Targets for TTN‐AS1 and miR‐15b‐5p were predicted by bioinformatic tools, and validated by luciferase activity reporter assay. Cell proliferation, colony formation, and cell apoptosis were analyzed with cell counting kit‐8 assay, colony formation assay, and flow cytometry. Correlation of TTN‐AS1 and FBXW7 was analyzed at gene expression profiling interactive analysis. TTN‐AS1 was found decreased expression in ovarian cancer tissues and cells. Dual‐luciferase activity validated TTN‐AS1 and FBXW7 shared binding site in miR‐15b‐5p. Functional assays showed TTN‐AS1 overexpression inhibits ovarian cancer cell proliferation, colony formation but promotes apoptosis. Rescue experiments showed that knockdown of FBXW7 could partially counteracted the effects of TTN‐AS1 overexpression on ovarian cancer cell behaviors. Our results indicated that the TTN‐AS1/miR‐15b‐5p/FBXW7 axis identified in this work could help to identify treatment biomarkers for ovarian cancer.

2Papers