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Published on: April 6, 2012
Long non-coding RNA RP11-379k17.4 derived microRNA-200c-3p modulates human endometrial cancer by targeting Noxa
Weijuan Xin1, Xiaodong Gao2, Peng Zhao3
1Department of Obstetrics and Gynecology, Obstetrics and Gynecology Hospital of Fudan University, 128 Shen-Yang Road, Shanghai 200090, China.
Abstract:
Objective: The research paid close attention to the function of lncRNA-related endogenous competitive RNAs (ceRNAs) network in endometrial cancer (EC). Methods: 45 primary endometrial cancer tissues (EC) and 45 normal endometrium (NE) were included in the research. The online software StarbaseV2.0 was made use of forecasting the lncRNA which most likely contained microRNA-200c-3p combining sites and could interact with microRNA-200c-3p. Subsequently, we chose lncRNAs which were consistent with the characteristics of polyadenylation of lncRNAs and lower expression in EC than that of NE. After that, lncRNAs, which were related with the microRNA-200c-3p-noxa network, were identified. Results: Rp11-379k17.4, a new gene related to endometrial cancer, was identified as noncoding RNA. It was a more effective ceRNA associated with the microRNA-200c-3p-noxa network. Conclusion: LncRNAs possess microRNA response elements (MREs) and give scope to significant roles in the post-transcriptional mechanism in EC.
Insights
This study identifies a novel long noncoding RNA (lncRNA) network involved in endometrial cancer (EC). This lncRNA-based ceRNA network plays a significant role in EC
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Endometrial cancer (EC) is a significant gynecological malignancy.
- Long noncoding RNAs (lncRNAs) are increasingly recognized for their roles in cancer.
- Endogenous competitive RNA (ceRNA) networks regulate gene expression post-transcriptionally.
Purpose of the Study:
- To investigate the function of lncRNA-related ceRNA networks in endometrial cancer.
- To identify specific lncRNAs interacting with microRNA-200c-3p in EC.
- To elucidate the role of the microRNA-200c-3p-noxa network in EC pathogenesis.
Main Methods:
- Analysis of 45 endometrial cancer tissues and 45 normal endometrium samples.
- Utilized StarbaseV2.0 to predict lncRNAs interacting with microRNA-200c-3p.
- Selected lncRNAs based on polyadenylation characteristics and differential expression in EC versus normal tissue.
Main Results:
- Identified Rp11-379k17.4, a novel noncoding RNA, as a key component of the EC ceRNA network.
- Rp11-379k17.4 demonstrated effective ceRNA activity within the microRNA-200c-3p-noxa network.
- The study highlights the dysregulation of specific lncRNAs in endometrial cancer.
Conclusions:
- LncRNAs with microRNA response elements (MREs) are crucial in EC post-transcriptional regulation.
- The identified lncRNA-ceRNA network, particularly involving Rp11-379k17.4, offers potential therapeutic targets for EC.
- Further research into lncRNA functions can advance understanding and treatment of endometrial cancer.
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