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Updated: May 29, 2025

Modeling the Early Steps of Ovarian Cancer Dissemination in an Organotypic Culture of the Human Peritoneal Cavity
Published on: December 31, 2015
CircMETTL6 Suppresses Ovarian Cancer Cell Growth and Metastasis Through Inhibition of GDF15 Transcription by
Mengqian Yu1, Mengting Wu1, Tao Shen2
1Zhejiang Key Laboratory of Precision Diagnosis and Therapy for Major Gynecological Diseases, Women's Hospital and Institute of Translational Medicine, Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310006, China.
Abstract:
Circular RNAs (circRNAs) are a distinctive class of non-coding RNAs with covalent closed-loop structure, lacking 5' caps and 3' poly(A) tails. These molecules are prevalent in eukaryotes and play key roles in cancer. Here, the function of a new circRNA, circMETTL6, in ovarian cancer is identified and investigated. The prognostic significance of circMETTL6 is assessed using RNA in situ hybridization. Functional studies involving circMETTL6 overexpression are performed both in vitro and in vivo. Mechanistic investigations are performed using RNA-seq, RNA pull-down, RNA immunoprecipitation, co-immunoprecipitation, chromatin immunoprecipitation, protein degradation assay and dual-luciferase reporter assays. circMETTL6 is significantly downregulated in ovarian cancer, and its lower expression correlates with worse prognosis. Overexpression of circMETTL6 significantly inhibited proliferation, migration, and invasion of ovarian cancer cell in vitro, as well as tumor growth and metastasis in vivo. Mechanistically, circMETTL6 recruited the non-POU domain containing octamer binding protein (NONO) by binding to its Coiled-coil domain and disrupted its binding with RNA polymerase II subunit A (POLR2A), and consequently inhibiting growth differentiation factor 15 (GDF15) transcription, thereby suppressing ovarian cancer progression. These findings establish circMETTL6 as a novel tumor suppressor in ovarian cancer. Targeting the circMETTL6/NONO/GDF15 axis presents a potential therapeutic avenue for ovarian cancer treatment.
Insights
Circular RNAs (circRNAs) act as tumor suppressors in ovarian cancer. The novel circRNA, circMETTL6, inhibits cancer progression by regulating the NONO/GDF15 pathway, offering a new therapeutic target.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Circular RNAs (circRNAs) are non-coding RNAs with a closed-loop structure.
- circRNAs play critical roles in eukaryotic gene regulation and are implicated in various cancers.
Purpose of the Study:
- To investigate the function and prognostic significance of a novel circRNA, circMETTL6, in ovarian cancer.
- To elucidate the underlying molecular mechanisms by which circMETTL6 affects ovarian cancer progression.
Main Methods:
- RNA in situ hybridization for prognostic assessment.
- In vitro and in vivo functional studies (overexpression).
- Molecular mechanism studies including RNA-seq, RNA pull-down, RIP, Co-IP, ChIP, protein degradation assays, and dual-luciferase reporter assays.
Main Results:
- circMETTL6 is significantly downregulated in ovarian cancer, correlating with poor prognosis.
- circMETTL6 overexpression suppressed ovarian cancer cell proliferation, migration, invasion, tumor growth, and metastasis.
- Mechanistically, circMETTL6 inhibits GDF15 transcription by disrupting the NONO-POLR2A interaction.
Conclusions:
- circMETTL6 functions as a novel tumor suppressor in ovarian cancer.
- The circMETTL6/NONO/GDF15 axis represents a potential therapeutic target for ovarian cancer treatment.
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