4.5 Article Proceedings Paper

The circular RNA expression profile in ovarian serous cystadenocarcinoma reveals a complex circRNA-miRNA regulatory network

期刊

BMC MEDICAL GENOMICS
卷 14, 期 SUPPL 2, 页码 -

出版社

BMC
DOI: 10.1186/s12920-021-01132-5

关键词

circRNA; Expression profile; Interaction network; Ovarian serous cystadenocarcinoma

资金

  1. National Natural Science Foundation of China [61973155]
  2. China Postdoctoral Science Foundation [2019M661817]

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This study revealed the expression profile of circRNAs in ovarian serous cystadenocarcinoma tissues, showing that the differential expression of circRNAs may be associated with the occurrence of ovarian serous cystadenocarcinoma. A complex circRNA-miRNA interaction network was constructed, demonstrating the potential functions of certain circRNAs for future diagnosis and treatment.
Background Ovarian serous cystadenocarcinoma is one of the most serious gynecological malignancies. Circular RNA (circRNA) is a type of noncoding RNA with a covalently closed continuous loop structure. Abnormal circRNA expression might be associated with tumorigenesis because of its complex biological mechanisms by, for example, functioning as a microRNA (miRNA) sponge. However, the circRNA expression profile in ovarian serous cystadenocarcinoma and their associations with other RNAs have not yet been characterized. The main purpose of this study was to reveal the circRNA expression profile in ovarian serous cystadenocarcinoma. Methods We collected six specimens from three patients with ovarian serous cystadenocarcinoma and adjacent normal tissues. After RNA sequencing, we analyzed the expression of circRNAs with relevant mRNAs and miRNAs to characterize potential function. Results 15,092 unique circRNAs were identified in six specimens. Approximately 46% of these circRNAs were not recorded in public databases. We then reported 353 differentially expressed circRNAs with oncogenes and tumor-suppressor genes. Furthermore, a conjoint analysis with relevant mRNAs revealed consistent changes between circRNAs and their homologous mRNAs. Overall, construction of a circRNA-miRNA network suggested that 4 special circRNAs could be used as potential biomarkers. Conclusions Our study revealed the circRNA expression profile in the tissues of patients with ovarian serous cystadenocarcinoma. The differential expression of circRNAs was thought to be associated with ovarian serous cystadenocarcinoma in the enrichment analysis, and co-expression analysis with relevant mRNAs and miRNAs illustrated the latent regulatory network. We also constructed a complex circRNA-miRNA interaction network and then demonstrated the potential function of certain circRNAs to aid future diagnosis and treatment.

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