Abstract

BackgroundOvarian 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.MethodsWe 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.Results15,092 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.ConclusionsOur 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.

Highlights

  • Ovarian serous cystadenocarcinoma is one of the most serious gynecological malignancies

  • Landscape of Circular RNA (circRNA) in ovarian serous cystadenocarcinoma Overall, we found 15,092 unique circRNAs with at least 2 junction reads spanning a head-to-tail splice junction

  • A total of 6500, 4370, and 2774 circRNAs were identified in the three tumor specimens, and 6201, 4932, and 5606 circRNAs were found in the three normal specimens (Fig. 1A)

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Summary

Introduction

Ovarian serous cystadenocarcinoma is one of the most serious gynecological malignancies. Abnormal circRNA expression might be associated with tumorigenesis because of its complex biological mechanisms by, for example, functioning as a microRNA (miRNA) sponge. 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. Dysregulation of special genes associated with adverse prognosis in ovarian cancer, such as p53 and VEGF, suggested that they have the potential to be used as biomarkers in diagnosis and treatment [4, 5]. The molecular mechanisms underlying ovarian serous cystadenocarcinoma remain unclear

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