# Elucidating Circular Ribonucleic Acid Mechanisms Associated with Splicing Factor 3 Inhibition in Cervical Cancer

## TL;DR

This study investigates how circular RNAs and a splicing factor inhibitor affect cervical cancer cells, suggesting theophylline could be a potential treatment.

## Contribution

The study identifies novel circular RNA-miRNA interactions and demonstrates the cytotoxic effects of theophylline in cervical cancer cell lines.

## Key findings

- Theophylline induces cell cycle arrest and apoptosis in cervical cancer cell lines.
- hsa_circ_0001038 interacts with miR-205-5p, a tumor-suppressive miRNA, while circRNA_400029 interacts with miR-16-5p.
- A ceRNA network and KEGG pathway analysis reveal key signaling pathways involved in cervical cancer progression.

## Abstract

Cervical cancer (CCa) is the fourth leading cause of cancer-related deaths among women worldwide, with nearly 90% of cases in low- and middle-income countries, especially in Sub-Saharan Africa. This study explores the roles of circular ribonucleic acids (circRNAs), hsa_circ_0001038 and circRNA_400029, and the impact of the serine/arginine-rich splicing factor 3 (SRSF3) inhibitor, theophylline, in CCa cell lines. We utilized cell cycle fluorescence-activated cell sorting (FACS) and Annexin V/propidium iodide (PI) assays to evaluate theophylline’s effects on SiHa and C33A cell lines. Results showed S-phase arrest in SiHa and G2/M arrest in C33A, with significant cytotoxic effects indicated by apoptosis analysis. Using CircAtlas, we identified micro ribonucleic acids (miRNAs) binding to hsa_circ_0001038, particularly miR-205-5p, which has a tumour-suppressive role. miRTarBase identified miR-16-5p as a key interacting miRNA for circRNA_400029. We constructed a competing endogenous ribonucleic acid (ceRNA) network, revealing multiple miRNA targets. Pathway analysis via the Kyoto Encyclopedia of Genes and Genomes (KEGG) highlighted critical signalling pathways involved in CCa oncogenesis. In conclusion, theophylline demonstrates cytotoxicity in CCa cells, suggesting its potential for repurposing in CCa theranostics, though further optimization is necessary.