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Murine Model for Non-invasive Imaging to Detect and Monitor Ovarian Cancer Recurrence
Published on: November 2, 2014
Deregulated circRNAs in Epithelial Ovarian Cancer With Activity in Preclinical In Vivo Models: Identification of
Ulrich H Weidle1, Fabian Birzele2
1Roche Pharma Research and Early Development, Roche Innovation Center Munich, Penzberg, Germany; weidle49@t-online.de.
Abstract:
Epithelial ovarian cancer (EOC) is associated with a dismal prognosis due to development of resistance to chemotherapy and metastasis in the peritoneal cavity and distant organs. In order to identify new targets and treatment modalities we searched the literature for up- and and down-regulated circRNAs with efficacy in preclinical EOC-related in vivo systems. Our search yielded circRNAs falling into the following categories: cisplatin and paclitaxel resistance, transmembrane receptors, secreted factors, transcription factors, RNA splicing and processing factors, RAS pathway-related components, proteolysis and cell-cycle regulation, signaling-related proteins, and circRNAs regulating proteins in additional categories. These findings can be potentially translated by validation and manipulation of the corresponding targets, inhibition of circRNAs with antisense oligonucleotides (ASO), small interfering RNAs (siRNA) or small hairpin RNA (shRNA) or by reconstituting their activity.
Insights
This study identifies circular RNAs (circRNAs) that are up- or down-regulated in epithelial ovarian cancer (EOC) models. These circRNAs offer potential new therapeutic targets for overcoming chemotherapy resistance and metastasis in EOC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Epithelial ovarian cancer (EOC) presents a poor prognosis due to chemoresistance and metastasis.
- Identifying novel therapeutic targets is crucial for improving EOC patient outcomes.
Purpose of the Study:
- To systematically review and categorize circular RNAs (circRNAs) implicated in epithelial ovarian cancer (EOC) preclinical models.
- To identify potential therapeutic targets and modalities for EOC treatment.
Main Methods:
- Literature search for up- and down-regulated circRNAs in preclinical in vivo EOC models.
- Categorization of identified circRNAs based on their biological functions and pathways.
Main Results:
- Identified circRNAs associated with cisplatin and paclitaxel resistance.
- Found circRNAs involved in transmembrane receptors, secreted factors, transcription factors, RNA processing, RAS pathway, and cell-cycle regulation.
- Highlighted circRNAs regulating signaling pathways and proteins in various categories.
Conclusions:
- Identified circRNAs represent promising targets for EOC therapy.
- Potential therapeutic strategies include target validation, circRNA inhibition (ASO, siRNA, shRNA), or reconstitution of activity.
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